** Categories not mutually exclusive.
The analysis cohort consisted of 18,965 opiate-positive cases and 78,838 test-negative controls. A quarter of both groups were female. Cases were older at their drug test (p < 0.001) and younger at their first recorded offence (p < 0.001). Cases were more likely to have a conviction for a serious acquisitive offence at this date (p < 0.001) and less likely to have a conviction for a violent offence (p < 0.001).
Sixty-seven per cent of opiate-positive cases had complete data on age-of-initiation. The majority of missing data were due to cases not having a linked treatment record (see Appendix A in the Supplementary material). The median age of initiation was similar for men and women.
Offending rates for four categories of offences.
All crimes | Non-serious acquisitive crimes | Serious acquisitive crimes | Violent crimes | |||||||
---|---|---|---|---|---|---|---|---|---|---|
Gender | Category | person years follow-up | Number | Rate [95% CI] | Number | Rate [95% CI] | Number | Rate [95% CI] | Number | Rate [95% CI] |
Male | non-users | 923,663 | 837,019 | 0.91 [0.90, 0.91] | 176,783 | 0.19 [0.19, 0.19] | 150,177 | 0.16 [0.16, 0.16] | 61,730 | 0.07 [0.07, 0.07] |
Opiate users | 290,007 | 528,153 | 1.82 [1.82, 1.83] | 153,031 | 0.53 [0.53, 0.53] | 103,654 | 0.36 [0.36, 0.36] | 25,247 | 0.09 [0.09, 0.09] | |
Pre-initiation | 96,491 | 115,682 | 1.20 [1.19, 1.21] | 25,285 | 0.26 [0.26, 0.27] | 34,317 | 0.36 [0.35, 0.36] | 6672 | 0.07 [0.07, 0.07] | |
Post-initiation | 97,788 | 270,885 | 2.77 [2.76, 2.78] | 91,148 | 0.93 [0.93, 0.94] | 40,917 | 0.42 [0.41, 0.42] | 10,796 | 0.11 [0.11, 0.11] | |
Initiation missing | 95,728 | 141,586 | 1.48 [1.47, 1.49] | 36,598 | 0.38 [0.38, 0.39] | 28,420 | 0.30 [0.29, 0.30] | 7779 | 0.08 [0.08, 0.08] | |
Female | non-users | 304,612 | 100,525 | 0.33 [0.33, 0.33] | 51,518 | 0.17 [0.17, 0.17] | 4194 | 0.01 [0.01, 0.01] | 8192 | 0.03 [0.03, 0.03] |
Opiate users | 87,373 | 120,336 | 1.38 [1.37, 1.39] | 66,637 | 0.76 [0.76, 0.77] | 4509 | 0.05 [0.05, 0.05] | 4840 | 0.06 [0.05, 0.06] | |
Pre-initiation | 32,839 | 15,139 | 0.46 [0.45, 0.47] | 8335 | 0.25 [0.25, 0.26] | 1096 | 0.03 [0.03, 0.04] | 1149 | 0.03 [0.03, 0.04] | |
Post-initiation | 29,807 | 80,056 | 2.69 [2.67, 2.70] | 44,767 | 1.50 [1.49, 1.52] | 2451 | 0.08 [0.08, 0.09] | 2523 | 0.08 [0.08, 0.09] | |
Initiation missing | 24,727 | 25,141 | 1.02 [1.00, 1.03] | 13,535 | 0.55 [0.54, 0.56] | 962 | 0.04 [0.04, 0.04] | 1168 | 0.05 [0.04, 0.05] |
In total, the cohort had 1.6 million sanctioned offences. For men, the rate of historical offending for opiate-positive cases was almost double that for test-negative controls (rate per year, opiate users: 1.82; non-users: 0.91; p < 0.001); the rate for opiate-positive females was more than four times that for test-negative females (opiate users: 1.38; non-users: 0.33; p < 0.001). For both male and female opiate users, the rate of offending was lower prior to initiation of opiate use compared to post-initiation. For males and females, the rate of violent and serious acquisitive offending peaked during the late teens, whilst the rate of non-serious acquisitive offences had a later peak ( Fig. 1 a and b).
Offending rates, per year by age, opiate users and non-users for: (a) male, non-serious acquisitive offences; (b) male, serious acquisitive offences; (c) male, violent offences; (d) female, non-serious acquisitive offences; (e) female, serious acquisitive offences; (f) female, violent offences.
Results of Generalised Estimating Equation analysis comparing historical offending rates of opiate users and non-users using whole sample (Model 1, N = 97,803) and those with complete data on age of initiation of opiate use (Model 2, N = 91,565), separately for males and females and for four categories of offences.
Male | Female | ||||||||
---|---|---|---|---|---|---|---|---|---|
Model 1 | Model 2 | Model 1 | Model 2 | ||||||
Offence category | Variable | RR | 95% CI | RR | 95% CI | RR | 95% CI | RR | 95% CI |
All crimes | Opiate users vs. non-users | 1.99 | [1.96, 2.01] | – | – | 4.59 | [4.48, 4.69] | – | – |
Initiation of opiate use | – | – | 1.16 | [1.15, 1.17] | – | – | 2.00 | [1.95, 2.05] | |
Users (pre-onset) vs. non-users | – | – | 2.00 | [1.97, 2.03] | – | – | 2.80 | [2.71, 2.90] | |
Users (post-onset) vs. non-users | – | – | 2.32 | [2.29, 2.35] | – | – | 5.61 | [5.47, 5.75] | |
Age | 1.92 | [1.92, 1.93] | 1.90 | [1.90, 1.91] | 2.53 | [2.51, 2.55] | 2.32 | [2.30, 2.34] | |
Age-squared | 0.77 | [0.77, 0.78] | 0.77 | [0.77, 0.77] | 0.78 | [0.78, 0.78] | 0.79 | [0.79, 0.79] | |
Age-cohort | |||||||||
<1975 | 0.75 | [0.74, 0.76] | 0.74 | [0.73, 0.75] | 0.62 | [0.60, 0.64] | 0.68 | [0.66, 0.70] | |
1975–1979 | 0.86 | [0.85, 0.87] | 0.85 | [0.84, 0.86] | 0.78 | [0.76, 0.80] | 0.82 | [0.79, 0.84] | |
1980–1984 | Ref | Ref | Ref | Ref | |||||
1985+ | 1.32 | [1.30, 1.34] | 1.33 | [1.31, 1.35] | 1.76 | [1.71, 1.82] | 1.71 | [1.65, 1.76] | |
Non-serious acquisitive | Opiate users vs. non-users | 2.65 | [2.61, 2.69] | – | – | 4.79 | [4.66, 4.91] | – | – |
Initiation of opiate use | – | – | 1.72 | [1.69, 1.75] | – | – | 2.18 | [2.11, 2.25] | |
Users (pre-onset) vs. non-users | – | – | 1.97 | [1.92, 2.02] | – | – | 2.73 | [2.62, 2.85] | |
Users (post-onset) vs. non-users | – | – | 3.39 | [3.34, 3.45] | – | – | 5.95 | [5.78, 6.12] | |
Age | 1.85 | [1.84, 1.85] | 1.74 | [1.73, 1.75] | 2.46 | [2.43, 2.48] | 2.23 | [2.20, 2.25] | |
Age-squared | 0.83 | [0.83, 0.83] | 0.83 | [0.83, 0.83] | 0.76 | [0.76, 0.77] | 0.78 | [0.77, 0.78] | |
Age-cohort | |||||||||
<1975 | 0.87 | [0.85, 0.89] | 0.92 | [0.90, 0.93] | 0.80 | [0.78, 0.83] | 0.90 | [0.87, 0.93] | |
1975–1979 | 0.95 | [0.93, 0.97] | 0.96 | [0.94, 0.98] | 0.88 | [0.85, 0.91] | 0.93 | [0.89, 0.96] | |
1980–1984 | Ref | Ref | Ref | Ref | |||||
1985+ | 1.08 | [1.05, 1.10] | 1.05 | [1.02, 1.07] | 1.30 | [1.25, 1.35] | 1.26 | [1.21, 1.32] | |
Serious acquisitive | Opiate users vs. non-users | 1.84 | [1.81, 1.87] | – | – | 4.11 | [3.85, 4.38] | – | – |
Initiation of opiate use | – | – | 1.25 | [1.22, 1.27] | – | – | 1.76 | [1.62, 1.92] | |
Users (pre-onset) vs. non-users | – | – | 1.87 | [1.82, 1.91] | – | – | 3.16 | [2.88, 3.46] | |
Users (post-onset) vs. non-users | – | – | 2.33 | [2.27, 2.38] | – | – | 5.58 | [5.19, 6.00] | |
Age | 1.16 | [1.15, 1.16] | 1.11 | [1.11, 1.12] | 1.39 | [1.36, 1.42] | 1.27 | [1.23, 1.30] | |
Age-squared | 0.66 | [0.66, 0.66] | 0.65 | [0.64, 0.65] | 0.81 | [0.80, 0.82] | 0.81 | [0.80, 0.83] | |
Age-cohort | |||||||||
<1975 | 0.83 | [0.81, 0.84] | 0.73 | [0.71, 0.75] | 0.75 | [0.69, 0.82] | 0.84 | [0.77, 0.93] | |
1975–1979 | 1.40 | [1.37, 1.43] | 1.39 | [1.36, 1.42] | 0.83 | [0.76, 0.91] | 0.90 | [0.82, 0.99] | |
1980–1984 | Ref | Ref | Ref | Ref | |||||
1985+ | 1.05 | [1.02, 1.07] | 1.06 | [1.04, 1.09] | 1.44 | [1.31, 1.57] | 1.46 | [1.33, 1.61] | |
Violent offences | Opiate users vs. non-users | 1.39 | [1.36, 1.42] | – | – | 2.42 | [2.30, 2.55] | – | – |
Initiation of opiate use | – | – | 0.75 | [0.72, 0.77] | – | – | 1.04 | [0.96, 1.13] | |
Users (pre-onset) vs. non-users | – | – | 1.79 | [1.72, 1.85] | – | – | 2.51 | [2.31, 2.72] | |
Users (post-onset) vs. non-users | – | – | 1.34 | [1.30, 1.37] | – | – | 2.61 | [2.45, 2.77] | |
Age | 1.85 | [1.84, 1.87] | 1.91 | [1.89, 1.93] | 1.79 | [1.76, 1.83] | 1.80 | [1.75, 1.84] | |
Age-squared | 0.80 | [0.80, 0.81] | 0.80 | [0.80, 0.80] | 0.88 | [0.87, 0.89] | 0.88 | [0.87, 0.89] | |
Age-cohort | |||||||||
<1975 | 0.71 | [0.69, 0.73] | 0.67 | [0.65, 0.69] | 0.43 | [0.40, 0.47] | 0.44 | [0.41, 0.48] | |
1975–1979 | 0.71 | [0.69, 0.73] | 0.69 | [0.67, 0.71] | 0.60 | [0.56, 0.65] | 0.61 | [0.56, 0.65] | |
1980–1984 | Ref | Ref | Ref | Ref | |||||
1985+ | 1.87 | [1.82, 1.92] | 1.92 | [1.86, 1.97] | 2.53 | [2.38, 2.70] | 2.59 | [2.43, 2.78] |
See Appendix D (Supplementary material) for rate within years.
Controlling for age, age-squared and age-cohort, male opiate positive’s prior total offending rate was double that for test-negatives (Rate Ratio: 1.99, 95% CI: 1.96–2.01); for females, it was over four times greater (RR: 4.59, 95% CI: 4.48–4.69). There was a relative increase in all categories of offending associated with being opiate-positive, with a greater increase for females than for males. The greatest increase associated with being an opiate–positive was for females and for the category non-serious acquisitive offending (RR: 4.79, 95% CI: 4.66–4.91). The lowest increase was for males and for the violent offences category.
The pre-initiation offending rate for male opiate-positive cases was double the rate for test-negative controls (RR = 2.00, 95% CI: 1.97–2.03), whilst the equivalent increased rate for females was 2.80 times (95% CI: 2.71–2.90). Initiation of opiate use increased the RR by 16% for males and 100% for females. Thus, the post-initiation rate was 2.32 times greater for cases than controls among males (95% CI: 2.29–2.35) and 5.61 times greater for females (95% CI: 5.47–5.75).
Both male and female cases had higher historical rates of non-serious and serious acquisitive offences prior to, and subsequent to, initiation of opiate use. For both serious and non-serious acquisitive offending categories and for both genders, initiation of opiate use increased the difference between cases and controls. Additionally, for both genders, there was a greater increase in the RR associated with initiation of opiate use for non-serious acquisitive crimes than serious crimes. In the case of violent offences, for females, the comparison between cases and controls was similar pre, and post, opiate-use initiation (RR: 2.51 and 2.61 respectively); the effect of opiate-use initiation in males was to reduce the RR (RR: 1.79 and 1.34).
We observed cohort effects; for example, controlling for age and drug-test status, later birth cohorts had higher rates of overall historical offending than earlier birth cohorts. However, this did not hold for the sub-categories of non-serious acquisitive crime, where each birth cohort had a similar rate of offending, or for serious acquisitive crime where, for men, earlier birth cohorts had a higher rate of offending.
A sensitivity analysis which separated the opiate-positive group into those that tested positive for opiates only and those that tested positive for opiates and cocaine, showed that the effect of opiate initiation was similar for both (see Appendix C in the Supplementary material).
4.1. summary of main findings.
Those testing positive for opiates had substantially higher rates of prior sanctioned offending over their life-course than those testing negative for opiates and cocaine. This finding held for both males and females, whilst controlling for age and birth cohort. Findings support our four a priori hypotheses regarding offending prior to, and post, opiate-use initiation: 1) opiate–positives had higher rates of offending than test-negative controls prior to their opiate-use onset; 2) initiation of opiate use exacerbates existing levels of offending compared to controls; 3) initiation of opiate use was associated with a larger increase in the rate ratio (RR) for female than male users; 4) the effect of opiate-use initiation on historical offending differs by crime type as well as by gender.
Of particular interest is the RR reduction in violent offending associated with opiate use initiation observed in male users; while for female users, the RR was relatively unchanged. Opiate-use initiation was associated with greater elevation in non-serious (e.g., shop-lifting) than serious (e.g., burglary) acquisitive crime for both male and female users.
Our previous work demonstrated the association between opiate use and recent offending, whilst highlighting that the strength of the association varies by gender and offence type ( Pierce et al., 2015 ). The present study expands on this analysis to investigate the longitudinal relationship between opiate-use initiation and crime. The majority of research carried out to examine the association between opiate use and crime has used a single cohort, pre/post design ( Hayhurst et al., 2017 ), rather than a separate control group. Our use of offending records over the life-course, together with a suitable control group of non-using offenders, whilst also controlling for age and birth cohort, are all important design strengths. Additionally, we use a large sample size (n = 18,965 cases; n = 78,838 controls) to supply the necessary statistical power needed to detect differences differentiated by gender and sub-category of offending.
The current study has some weaknesses. First, the use of a retrospective design limits the inferences that can be made – for instance, we cannot assess the influence that prior offending has on the likelihood of future opiate use. We are unable to hypothesise the extent to which offending prior to opiate-use initiation is associated with use of other substances, such as cannabis or alcohol, which may precede opiate use initiation ( Lessem et al., 2006 , Lynskey, 2003 ). Also, the opiate-using cohort may not be representative of opiate users in general. The cohort is sampled from individuals who received a drug test on arrest and were subsequently sanctioned; therefore, it is of greater relevance to opiate-using offenders.
The measures used are imperfect. Drug-using offenders may be more likely than non-users to be apprehended ( Bond and Sheridan, 2007 , Stevens, 2008 ) due, for example, to intoxication leading to easier identification. This may account for some of the differences detected in the current analysis, and, potentially, for differences in the period prior to initiation of opiate use, during which the likelihood of arrest may be affected by misuse of other substances, but this explanation is unlikely to account for the strength of the association observed here. Our work corresponds with previous research highlighting high levels of offending in opiate users prior to opiate-use onset ( Shaffer et al., 1987 ); suggestive of common factors underlying both behaviours. Additionally, misclassification of non-cases was evident: 7% of negative testers were linked to an NDTMS record confirming drug-user status. Cases were identified via a saliva test which, despite having high sensitivity and specificity ( Kacinko et al., 2004 ), only detects opiates used up to 24 h prior to testing( Verstraete, 2004 ) and so may not have identified less-problematic users. Any such misclassification would mean that the opiate-user and non-user group identified in this study are more similar than they would be under any ‘gold-standard’ testing procedure, meaning that the results presented are likely to be overly conservative, therefore not disputing our conclusions.
There was missing information on age of initiation for 33% of opiate positive testers; the majority because they did not have a treatment record over the data collection period. Secondary analysis of those with missing data (see Appendix A in the Supplementary material) showed that those who were not linked to NDTMS were less likely to test positive for both opiates and cocaine and were more likely to be male. Inspection of the graphs of offending rate by age group shows that those with missing linkage to NDTMS records had lower rates of offending over the life-course than those with complete information (see Appendix E in the Supplementary material). This could be because individuals who had not sought treatment were a shorter time into their using careers and not caught in a cycle of addiction and offending seen among those in this analysis. Therefore, the generalisability of these results might be affected by our focus on those individuals with a linked treatment record (75% of our cohort).
The findings of the present study are subject to unmeasured confounding. Information on important social factors, such as substance use or criminal behaviour among family members, was not available; neither was socio-economic status ( Gauffin et al., 2013 ). However, even if suitable data were available, it may be difficult to establish the temporal ordering of change in socio-economic status and drug-use initiation.
Our findings are directly relevant to Government drug policy as they are derived from individuals who have persisted in both their opiate use and offending. The findings confirm the relationship between opiate use and offending observed by others ( Bennett et al., 2008 , Bukten et al., 2011 ). We were also able to demonstrate that opiate-use onset is associated with crime escalation, independent of changes which occur with age. Therefore, initiation of opiate use appears to be a crucial driver of offending; measures to reduce offending should include drug-use prevention.
Others have highlighted that onset substance use in offenders impedes the process of “maturing” out of crime described by the age-crime curve ( Hussong et al., 2004 , Ouimet and Le Blanc, 1996 , Schroeder et al., 2007 ). Greater escalation of offending, compared to controls, post-opiate initiation, was seen in female than male users. This confirms the findings of a recent review, which indicated lower offence rates pre-opiate use in females than males but a greater escalation of crime subsequent to opiate-use onset in females ( Hayhurst et al., 2017 ).
The absence of a relationship between violent crime and onset-opiate use in this study is of significance. Our previous work found a strong association between women testing positive for opiate use and recent violent offending, although such offences were only recorded in 8% of women ( Pierce et al., 2015 ). The current study indicates no apparent increase in violent offending by women associated with opiate initiation, and a relative reduction in violent crime for men. This finding tallies with previous research indicating no confirmed relationship between violent crime and onset-substance use ( Parker and Auerhahn, 1998 , White and Gorman, 2000 ).
The large impact of opiate-use initiation on non-serious acquisitive crime mirrors that of our previous work, which demonstrated a rate of shoplifting in opiate users that was between 3.5 (males) and 4.7 (females) times that of non-using offenders ( Pierce et al., 2015 ). These findings could be explained by opiate users focussing on criminal activity that generates sufficient income to support current drug use and that is within the skill set of the individual user ( James et al., 1979 ).
Previous research indicated greater increases in offending levels post-opiate use in individuals with onset of opiate use at an earlier age ( Hayhurst et al., 2017 ). This corresponds with key offending theories in demonstrating that early antisocial or delinquent behaviour is associated with a more pronounced offending trajectory ( Moffitt, 1993 ). It would be informative to examine this interaction further with the use of a control cohort. It would also be advantageous to analyse prospective, longitudinal cohorts so that information could be incorporated on those who desist in their offending and opiate use.
We have previously highlighted a surprising lack of high-quality research with which to delineate the nature of the relationship between drug use, in general, and opiate use, in particular, and crime. This is one of a handful of studies to employ a control group to account for the well-known relationship between age, drug use and crime. Findings indicate a more complex drugs-crime relationship than that espoused by current drug policy ( Home Office, 2010 ) with already higher than expected levels of offending in those who go on to use drugs, such as opiates, problematically and whose offending behaviour then escalates. Having a more nuanced understanding of the nature of the drugs-crime relationship is crucial to the development of policy responses underpinning decisions about how best to intervene to interrupt the pathway from onset crime to onset substance use ( Hayhurst et al., 2017 ). Findings suggest that complex interventions that target young, particularly female, offenders are required. Indeed, our findings align with the conclusions of others who have suggested that it is quite viable to identify future problematic substance users by patterns of early-life delinquent and offending behaviour, allowing for targeted intervention ( Macleod et al., 2013 ).
This research was funded as part of the Insights study by the UK Medical Research Council (MR/J013560/1). The MRC had no further role in study design; in the collection, analysis and interpretation of data; in the writing of the report; or in the decision to submit the paper for publication. The Home Office have been provided with a pre-submission version of this manuscript but have not exerted any editorial control over, or commented on, its content. Sheila Bird is funded by Medical Research Council programme number MC_U105260794.
Millar , Pierce and Hayhurst conceived of the study. Pierce with input from Bird wrote the analysis plan. Pierce analysed the data and wrote a first draft of the manuscript. Millar , Bird and Dunn supervised data analysis. All interpreted the data, edited, and approved of the manuscript.
Millar has received research funding from the UK National Treatment Agency for Substance Misuse and the Home Office. He has been a member of the organising committee for conferences supported by unrestricted educational grants from Reckitt Benckiser, Lundbeck, Martindale Pharma, and Britannia Pharmaceuticals Ltd, for which he received no personal remuneration. He is a member of the Advisory Council on the Misuse of Drugs. Bird holds GSK shares. She is formerly an MRC programme leader and has been elected to Honorary Professorship at Edinburgh University. She chaired Home Office’s Surveys, Design and Statistics Subcommittee (SDSSC) when SDSSC published its report on 21st Century Drugs and Statistical Science. She has previously served as UK representative on the Scientific Committee for European Monitoring Centre for Drugs and Drug Addiction. She is co-principal investigator for MRC-funded, prison-based N-ALIVE pilot Trial. Seddon has received research funding from the UK National Treatment Agency for Substance Misuse and the Home Office. Hayhurst has received grant research funding from Change, Grow, Live (CGL), a 3rd-sector provider of substance misuse services.
A number of organisations and individuals enabled access to data to support this research, including: The Home Office, The Ministry of Justice, Dr Sara Skodbo, Maryam Ahmad, Anna Richardson, Hannah Whitehead, and Nick Manton.
Appendix A Supplementary data associated with this article can be found, in the online version, at http://dx.doi.org/10.1016/j.drugalcdep.2017.07.024 .
The following is Supplementary data to this article:
National Institutes of Health ( NIH )
R36 Dissertation Award
See Section III. 3. Additional Information on Eligibility .
The goal of this Notice of Funding Opportunity (NOFO) is to support doctoral candidates from a variety of academic disciplines for up to two years for the completion of the doctoral dissertation research project. Research projects should align with the NIDA Strategic Plan ( 2022-2026 NIDA Strategic Plan Director's Message | National Institute on Drug Abuse (NIDA) (nih.gov) . This award will facilitate the entry of promising new investigators into the field of substance use/substance use disorder (SU(D) research, enhancing the pool of highly trained SU(D) researchers. Applications are particularly encouraged from individuals from diverse backgrounds, including those from underrepresented groups as described in the Notice of NIH's Interest in Diversity ( NOT-OD-20-031 ).
This NOFO is designed specifically for applicants proposing research that does not involve leading an independent clinical trial, a clinical trial feasibility study, or an ancillary clinical trial. Applicants to this NOFO are permitted to propose research experience in a clinical trial led by a mentor or co-mentor.
Not Required
The following table includes NIH standard due dates marked with an asterisk.
Dates in bold and italics reflect changes per NOT-DA-24-030
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Conformance to all requirements (both in the Application Guide and the NOFO) is required and strictly enforced. Applicants must read and follow all application instructions in the Application Guide as well as any program-specific instructions noted in Section IV. When the program-specific instructions deviate from those in the Application Guide, follow the program-specific instructions.
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Section i. notice of funding opportunity description.
The goal of this Notice of Funding Opportunity (NOFO) is to support doctoral candidates from a variety of academic disciplines for up to two years for the completion of the doctoral dissertation research project. Dissertation research topics should align with the National Institute on Drug Abuse (NIDA) strategic plan ( https://nida.nih.gov/about-nida/noras-blog/2022/09/nida-releases-its-2022-2026-strategic-plan ), or with the NIDA HIV/AIDS research priorities ( https://nida.nih.gov/about-nida/organization/offices/hiv-research-program-hrp/about-hiv-research-program ). This program will ultimately facilitate the entry of promising new investigators into the field of substance use/substance use disorder (SU/D) research.
Every facet of the United States scientific research enterprise from basic laboratory research to clinical and translational research to policy formation requires superior intellect, creativity and a wide range of skill sets and viewpoints. NIH’s ability to help ensure that the nation remains a global leader in scientific discovery and innovation is dependent upon a pool of highly talented scientists from diverse backgrounds who will help to further NIH's mission. ( NOT-OD-20-031 ).
Research Objectives
Research supported by NIDA encompasses the underlying mechanisms and health effects of SU/D. This NOFO provides students with funding to conduct dissertation research in support of NIDA's mission. Research may be related to basic neuroscience, etiology, epidemiology, prevention, treatment, services, or women and sex/gender differences. Please view NIDAs current Strategic Plan ( https://nida.nih.gov/about-nida/noras-blog/2022/09/nida-releases-its-2022-2026-strategic-plan ) for more information. This program is intended to encourage investigators to seek research careers that will reduce the health, social, and financial costs of substance use disorders (SUD) to society.
NIDA supports projects that enable doctoral degree candidates to receive training in clinical research, including clinical trials. However, trainees cannot be supported under the R36 mechanism to conduct independent clinical trials (see https://grants.nih.gov/policy/clinical-trials/definition.htm for a definition). If the R36 project involves a proposed or ongoing clinical trial, the trial must be led by a mentor or a more experienced investigator, who is responsible for completing all required approvals. The doctoral candidate can be a part of the research team and can use the data generated during the clinical trial in the proposed project. However, the research experience of the doctoral candidate must be supervised by a more experienced Principal Investigator (PI).
The descriptions below are examples of research areas supported by this program and are provided to help potential applicants determine whether a particular scientific topic is appropriate for this initiative. These descriptions are not intended to be comprehensive. In addition, given the complexity of SU/D research, it is permitted to conduct the proposed dissertation research in conjunction with an ongoing research study or to use extant data. Research studies focused on high-priority NIDA HIV/AIDS topics ( https://nida.nih.gov/about-nida/organization/offices/hiv-research-program-hrp/about-hiv-research-program ) and minority health and NIH-designated populations that experience health disparities (including racial and ethnic minority populations, less privileged socioeconomic status (SES) populations, underserved rural populations, and sexual and gender minorities (SGM)) are also encouraged. Applicants are strongly encouraged to discuss their proposed research plan with a program official.
Basic Neuroscience
Etiology and Epidemiology
Women and Sex/Gender Differences
Through this dissertation award program, NIDA seeks to foster research on females (both humans and in animal models) and sex/gender differences in all areas of substance use research. From basic cellular and genetics research to epidemiology, prevention, treatment, and services research, investigators are encouraged to explore the possible importance of sex/gender differences in their chosen area of study and to explore substance use issues specific to females.
Examples of research areas appropriate for this announcement include:
Applications Not Responsive to this NOFO
Application lacking the following will be considered non-responsive and will not be reviewed:
Special Considerations
NIDA applicants are strongly encouraged to review the guidelines and adhere to the requirements applicable to their research listed in the Special Considerations for NIDA Funding Opportunities and Awards . Upon award, these considerations will be included in the Notice of Grant Award.
See Section VIII. Other Information for award authorities and regulations.
Grant: A support mechanism providing money, property, or both to an eligible entity to carry out an approved project or activity.
The OER Glossary and the SF424 (R&R) Application Guide provide details on these application types. Only those application types listed here are allowed for this NOFO.
Not Allowed: Only accepting applications that do not propose clinical trials.
Need help determining whether you are doing a clinical trial?
The number of awards is contingent upon NIH appropriations and the submission of a sufficient number of meritorious applications.
Grants to support dissertation research will provide no more than $50,000 in direct costs per year. The salary proposed must be appropriately related to the existing salary structure at the recipient institution.
Indirect Costs (also known as Facilities & Administrative [F&A] Costs) are reimbursed at 8% of modified total direct costs (exclusive of tuition and fees, consortium costs in excess of $25,000, and expenditures for equipment), rather than on the basis of a negotiated rate agreement.
Applications may request a minimum of one and a maximum of two years of support.
NIH grants policies as described in the NIH Grants Policy Statement will apply to the applications submitted and awards made from this NOFO.
1. Eligible Applicants
Higher Education Institutions
The following types of Higher Education Institutions are always encouraged to apply for NIH support as Public or Private Institutions of Higher Education:
Nonprofits Other Than Institutions of Higher Education
For-Profit Organizations
Local Governments
Federal Government
Non-domestic (non-U.S.) Entities (Foreign Institutions) are not eligible to apply.
Non-domestic (non-U.S.) components of U.S. Organizations are not eligible to apply.
Foreign components, as defined in the NIH Grants Policy Statement , are allowed.
Applicant Organizations
Applicant organizations must complete and maintain the following registrations as described in the SF 424 (R&R) Application Guide to be eligible to apply for or receive an award. All registrations must be completed prior to the application being submitted. Registration can take 6 weeks or more, so applicants should begin the registration process as soon as possible. The NIH Policy on Late Submission of Grant Applications states that failure to complete registrations in advance of a due date is not a valid reason for a late submission.
Program Directors/Principal Investigators (PD(s)/PI(s))
All PD(s)/PI(s) must have an eRA Commons account. PD(s)/PI(s) should work with their organizational officials to either create a new account or to affiliate their existing account with the applicant organization in eRA Commons. If the PD/PI is also the organizational Signing Official, they must have two distinct eRA Commons accounts, one for each role. Obtaining an eRA Commons account can take up to 2 weeks.
By the time of award, the dissertation candidate must be a citizen or a non-citizen national of the United States or have been lawfully admitted for permanent residence (i.e., possess a currently valid Permanent Resident Card USCIS Form I-551, or other legal verification of such status). Furthermore, at the time of award the applicant must have completed all institutional requirements to enter the dissertation stage of their research program.
Trainees who have received F31 funding are ineligible for the R36 Dissertation Award. Concurrent F31 and R36 applications are not allowed. Multiple PD/PI applications are not allowed.
2. Cost Sharing
This NOFO does not require cost sharing as defined in the NIH Grants Policy Statement.
3. Additional Information on Eligibility
Number of Applications
Applicant organizations may submit more than one application, provided that each application is scientifically distinct.
The NIH will not accept duplicate or highly overlapping applications under review at the same time, per 2.3.7.4 Submission of Resubmission Application . This means that the NIH will not accept:
1. Requesting an Application Package
The application forms package specific to this opportunity must be accessed through ASSIST, Grants.gov Workspace or an institutional system-to-system solution. Links to apply using ASSIST or Grants.gov Workspace are available in Part 1 of this NOFO. See your administrative office for instructions if you plan to use an institutional system-to-system solution.
2. Content and Form of Application Submission
It is critical that applicants follow the instructions in the Research (R) Instructions in the SF424 (R&R) Application Guide except where instructed in this notice of funding opportunity to do otherwise. Conformance to the requirements in the Application Guide is required and strictly enforced. Applications that are out of compliance with these instructions may be delayed or not accepted for review.
All page limitations described in the SF424 Application Guide and the Table of Page Limits must be followed.
The following section supplements the instructions found in the SF424 (R&R) Application Guide and should be used for preparing an application to this NOFO.
All instructions in the SF424 (R&R) Application Guide must be followed.
Other Attachments:
Instruction in the Responsible Conduct of Research (required): All applications must include a plan to fulfill NIH requirements for Instruction in the Responsible Conduct of Research (RCR). The attachment is limited to one page. The plan must address the five, required instructional components outlined in the NIH policy: 1) Format - the required format of instruction, i.e., face-to-face lectures, coursework, and/or real-time discussion groups (a plan with only on-line instruction is not acceptable); 2) Subject Matter - the breadth of subject matter, e.g., conflict of interest, authorship, data management, human subjects and animal use, laboratory safety, research misconduct, research ethics; 3) Faculty Participation - the role of the mentor(s) and other faculty involvement in the instruction; 4) Duration of Instruction - the number of contact hours of instruction; and 5) Frequency of Instruction instruction must occur during each career stage and at least once every four years. Document any prior instruction during the applicant’s current career stage, including the inclusive dates instruction was last completed. See also NOT-OD-10-019 .
Scientific Support Plan (required) : All applications must include a plan for scientific support of the PD/PI. The attachment is limited to two pages. Outline activities that will ensure that the PD/PI has a thorough understanding of the scientific principles and methods required for the proposed study. Describe plans for professional skills development to assist the PD/PI to transition to the next stage of their research career. Highlight the time to be allocated by the advisor to guide and support the PD/PI so that they will complete the dissertation in a timely manner.
All instructions in the SF424 (R&R) Application Guide must be followed, with the following additional instructions.
Biographical Sketches must be provided for the PD/PI and the dissertation project advisor, and include the following:
R&R Subaward Budget
All instructions in the SF424 (R&R) Application Guide must be followed, with the following additional instructions:
Research Strategy
Letters of Support: All letters must be combined into a single PDF file.?
Letter of Certification (required): The faculty advisor, dissertation committee chair, or university official directly responsible for supervising the dissertation research must submit a letter certifying that the PD/PI meets the eligibility criteria for this award.
Advisor and Reference Letters (required): The faculty advisor and at least one other member of the dissertation committee must submit letters, each no longer than 2 pages, that assess (a) the doctoral candidate’s progress to date; and (b) the candidate’s commitment to SU(D) research and their prospect of becoming an independent investigator in this area. The letters must address the institutional support and resources available to foster the completion of the dissertation project in a timely manner.
Resource Sharing Plan:
Individuals are required to comply with the instructions for the Resource Sharing Plans as provided in the SF424 (R& R ) Application Guide.
Other Plan(s):
Note: Effective for due dates on or after January 25, 2023, the Data Management and Sharing Plan will be attached in the Other Plan(s) attachment in FORMS-H application forms packages.
A Data Management and Sharing Plan is not applicable for this NOFO.
Only limited Appendix materials are allowed. Follow all instructions for the Appendix as described in the SF424 (R&R) Application Guide.
When involving human subjects research, clinical research, and/or NIH-defined clinical trials (and when applicable, clinical trials research experience) follow all instructions for the PHS Human Subjects and Clinical Trials Information form in the SF424 (R&R) Application Guide, with the following additional instructions:
If you answered Yes to the question Are Human Subjects Involved? on the R&R Other Project Information form, you must include at least one human subjects study record using the Study Record: PHS Human Subjects and Clinical Trials Information form or Delayed Onset Study record.
Study Record: PHS Human Subjects and Clinical Trials Information
Delayed Onset Study
Note: Delayed onset does NOT apply to a study that can be described but will not start immediately (i.e., delayed start). All instructions in the SF424 (R&R) Application Guide must be followed.
3. Unique Entity Identifier and System for Award Management (SAM)
See Part 1. Section III.1 for information regarding the requirement for obtaining a unique entity identifier and for completing and maintaining active registrations in System for Award Management (SAM), NATO Commercial and Government Entity (NCAGE) Code (if applicable), eRA Commons, and Grants.gov
Part I. Overview Information contains information about Key Dates and times. Applicants are encouraged to submit applications before the due date to ensure they have time to make any application corrections that might be necessary for successful submission. When a submission date falls on a weekend or Federal holiday , the application deadline is automatically extended to the next business day.
Organizations must submit applications to Grants.gov (the online portal to find and apply for grants across all Federal agencies). Applicants must then complete the submission process by tracking the status of the application in the eRA Commons , NIH’s electronic system for grants administration. NIH and Grants.gov systems check the application against many of the application instructions upon submission. Errors must be corrected and a changed/corrected application must be submitted to Grants.gov on or before the application due date and time. If a Changed/Corrected application is submitted after the deadline, the application will be considered late. Applications that miss the due date and time are subjected to the NIH Policy on Late Application Submission.
Applicants are responsible for viewing their application before the due date in the eRA Commons to ensure accurate and successful submission.
Information on the submission process and a definition of on-time submission are provided in the SF424 (R&R) Application Guide.
5. Intergovernmental Review (E.O. 12372)
This initiative is not subject to intergovernmental review.
All NIH awards are subject to the terms and conditions, cost principles, and other considerations described in the NIH Grants Policy Statement .
Pre-award costs are allowable only as described in the NIH Grants Policy Statement .
Applications must be submitted electronically following the instructions described in the SF424 (R&R) Application Guide. Paper applications will not be accepted.
Applicants must complete all required registrations before the application due date. Section III. Eligibility Information contains information about registration.
For assistance with your electronic application or for more information on the electronic submission process, visit How to Apply Application Guide . If you encounter a system issue beyond your control that threatens your ability to complete the submission process on-time, you must follow the Dealing with System Issues guidance. For assistance with application submission, contact the Application Submission Contacts in Section VII .
Important reminders:
All PD(s)/PI(s) must include their eRA Commons ID in the Credential field of the Senior/Key Person Profile form . Failure to register in the Commons and to include a valid PD/PI Commons ID in the credential field will prevent the successful submission of an electronic application to NIH. See Section III of this NOFO for information on registration requirements.
The applicant organization must ensure that the unique entity identifier provided on the application is the same identifier used in the organization’s profile in the eRA Commons and for the System for Award Management. Additional information may be found in the SF424 (R&R) Application Guide.
See more tips for avoiding common errors.
Upon receipt, applications will be evaluated for completeness and compliance with application instructions by the Center for Scientific Review and responsiveness by NIDA, NIH. Applications that are incomplete, non-compliant and/or nonresponsive will not be reviewed.
Applicants are required to follow the instructions for post-submission materials, as described in the policy
1. Criteria
Only the review criteria described below will be considered in the review process. Applications submitted to the NIH in support of the NIH mission are evaluated for scientific and technical merit through the NIH peer review system.
Overall Impact
Reviewers will provide an overall impact score to reflect their assessment of the likelihood for the project to exert a sustained, powerful influence on the research field(s) involved, in consideration of the following review criteria and additional review criteria (as applicable for the project proposed).
Scored Review Criteria
Reviewers will consider each of the review criteria below in the determination of scientific merit and give a separate score for each. An application does not need to be strong in all categories to be judged likely to have major scientific impact. For example, a project that by its nature is not innovative may be essential to advance a field.
Significance
Does the project address an important problem or a critical barrier to progress in the field? Is the prior research that serves as the key support for the proposed project rigorous? If the aims of the project are achieved, how will scientific knowledge, technical capability, and/or clinical practice be improved? How will successful completion of the aims change the concepts, methods, technologies, treatments, services, or preventative interventions that drive this field?
Specific to this NOFO: significance should be evaluated within the context of a doctoral dissertation: to what extent will successful completion of the project help the PD/PI to advance their research career goals?
Investigator(s)
Are the PD(s)/PI(s), collaborators, and other researchers well suited to the project? If Early Stage Investigators or those in the early stages of independent careers, do they have appropriate experience and training? If established, have they demonstrated an ongoing record of accomplishments that have advanced their field(s)? If the project is collaborative or multi-PD/PI, do the investigators have complementary and integrated expertise; are their leadership approach, governance, and organizational structure appropriate for the project?
Specific to this NOFO: How strong is the promise of the PD/PI as a research investigator in research areas relevant to the application, as evidenced in their Biographical Sketch and letters of support? How well-qualified is/are the advisor(s) to provide guidance, i.e., how strong is their mentoring experience? How adequate is the time allocated by the faculty advisor to guide and support the PD/PI so that he/she will complete the dissertation in a timely manner?
Does the application challenge and seek to shift current research or clinical practice paradigms by utilizing novel theoretical concepts, approaches or methodologies, instrumentation, or interventions? Are the concepts, approaches or methodologies, instrumentation, or interventions novel to one field of research or novel in a broad sense? Is a refinement, improvement, or new application of theoretical concepts, approaches or methodologies, instrumentation, or interventions proposed?
Specific to this NOFO: Innovation should be considered within the context of the doctoral dissertation - how appropriate is the level of innovation as compared to the PD/PI’s career stage?
Are the overall strategy, methodology, and analyses well-reasoned and appropriate to accomplish the specific aims of the project? Have the investigators included plans to address weaknesses in the rigor of prior research that serves as the key support for the proposed project? Have the investigators presented strategies to ensure a robust and unbiased approach, as appropriate for the work proposed? Are potential problems, alternative strategies, and benchmarks for success presented? If the project is in the early stages of development, will the strategy establish feasibility and will particularly risky aspects be managed? Have the investigators presented adequate plans to address relevant biological variables, such as sex, for studies in vertebrate animals or human subjects?
If the project involves human subjects and/or NIH-defined clinical research, are the plans to address 1) the protection of human subjects from research risks, and 2) inclusion (or exclusion) of individuals on the basis of sex/gender, race, and ethnicity, as well as the inclusion or exclusion of individuals of all ages (including children and older adults), justified in terms of the scientific goals and research strategy proposed?
Specific to this NOFO: How adequate are the proposed activities in ensuring that the PD/PI will have a thorough understanding of the scientific principles and methods required for the proposed study? How strong are plans for professional skills development to assist the PD/PI to transition to the next stage of their research career? How strong is the proposed plan for instruction in the responsible conduct of research?
Environment
Will the scientific environment in which the work will be done contribute to the probability of success? Are the institutional support, equipment, and other physical resources available to the investigators adequate for the project proposed? Will the project benefit from unique features of the scientific environment, subject populations, or collaborative arrangements?
Specific to this NOFO: is there sufficient institutional support to foster completion of the dissertation project in a timely manner, as evidenced by the letters of support?
Additional Review Criteria
As applicable for the project proposed, reviewers will evaluate the following additional items while determining scientific and technical merit, and in providing an overall impact score, but will not give separate scores for these items.
Protections for Human Subjects
For research that involves human subjects but does not involve one of the categories of research that are exempt under 45 CFR Part 46, the committee will evaluate the justification for involvement of human subjects and the proposed protections from research risk relating to their participation according to the following five review criteria: 1) risk to subjects, 2) adequacy of protection against risks, 3) potential benefits to the subjects and others, 4) importance of the knowledge to be gained, and 5) data and safety monitoring for clinical trials.
For research that involves human subjects and meets the criteria for one or more of the categories of research that are exempt under 45 CFR Part 46, the committee will evaluate: 1) the justification for the exemption, 2) human subjects involvement and characteristics, and 3) sources of materials. For additional information on review of the Human Subjects section, please refer to the Guidelines for the Review of Human Subjects .
Inclusion of Women, Minorities, and Individuals Across the Lifespan
When the proposed project involves human subjects and/or NIH-defined clinical research, the committee will evaluate the proposed plans for the inclusion (or exclusion) of individuals on the basis of sex/gender, race, and ethnicity, as well as the inclusion (or exclusion) of individuals of all ages (including children and older adults) to determine if it is justified in terms of the scientific goals and research strategy proposed. For additional information on review of the Inclusion section, please refer to the Guidelines for the Review of Inclusion in Clinical Research .
Vertebrate Animals
The committee will evaluate the involvement of live vertebrate animals as part of the scientific assessment according to the following criteria: (1) description of proposed procedures involving animals, including species, strains, ages, sex, and total number to be used; (2) justifications for the use of animals versus alternative models and for the appropriateness of the species proposed; (3) interventions to minimize discomfort, distress, pain and injury; and (4) justification for euthanasia method if NOT consistent with the AVMA Guidelines for the Euthanasia of Animals. Reviewers will assess the use of chimpanzees as they would any other application proposing the use of vertebrate animals. For additional information on review of the Vertebrate Animals section, please refer to the Worksheet for Review of the Vertebrate Animals Section .
Reviewers will assess whether materials or procedures proposed are potentially hazardous to research personnel and/or the environment, and if needed, determine whether adequate protection is proposed.
Resubmissions
For Resubmissions, the committee will evaluate the application as now presented, taking into consideration the responses to comments from the previous scientific review group and changes made to the project.
Not applicable
As applicable for the project proposed, reviewers will consider each of the following items, but will not give scores for these items, and should not consider them in providing an overall impact score.
Applications from Foreign Organizations
Not Applicable.
Select Agent Research
Reviewers will assess the information provided in this section of the application, including 1) the Select Agent(s) to be used in the proposed research, 2) the registration status of all entities where Select Agent(s) will be used, 3) the procedures that will be used to monitor possession use and transfer of Select Agent(s), and 4) plans for appropriate biosafety, biocontainment, and security of the Select Agent(s).
Resource Sharing Plans
Reviewers will comment on whether the Resource Sharing Plan(s) (i.e., Sharing Model Organisms ) or the rationale for not sharing the resources, is reasonable.
Authentication of Key Biological and/or Chemical Resources:
For projects involving key biological and/or chemical resources, reviewers will comment on the brief plans proposed for identifying and ensuring the validity of those resources.
Budget and Period of Support
Reviewers will consider whether the budget and the requested period of support are fully justified and reasonable in relation to the proposed research.
Applications will be evaluated for scientific and technical merit by (an) appropriate Scientific Review Group(s) convened by the Center for Scientific Review, in accordance with NIH peer review policy and procedures , using the stated review criteria. Assignment to a Scientific Review Group will be shown in the eRA Commons.
As part of the scientific peer review, all applications will receive a written critique.
Applications may undergo a selection process in which only those applications deemed to have the highest scientific and technical merit (generally the top half of applications under review) will be discussed and assigned an overall impact score.
Applications will be assigned to the appropriate NIH Institute or Center. Applications will compete for available funds with all other recommended applications. Following initial peer review, recommended applications will receive a second level of review by the National Advisory Council for Drug Abuse. The following will be considered in making funding decisions:
3. Anticipated Announcement and Award Dates
After the peer review of the application is completed, the PD/PI will be able to access his or her Summary Statement (written critique) via the eRA Commons . Refer to Part 1 for dates for peer review, advisory council review, and earliest start date.
Information regarding the disposition of applications is available in the NIH Grants Policy Statement .
1. Award Notices
If the application is under consideration for funding, NIH will request "just-in-time" information from the applicant as described in the NIH Grants Policy Statement .
A formal notification in the form of a Notice of Award (NoA) will be provided to the applicant organization for successful applications. The NoA signed by the grants management officer is the authorizing document and will be sent via email to the recipient's business official.
Recipients must comply with any funding restrictions described in Section IV.5. Funding Restrictions. Selection of an application for award is not an authorization to begin performance. Any costs incurred before receipt of the NoA are at the recipient's risk. These costs may be reimbursed only to the extent considered allowable pre-award costs.
Any application awarded in response to this NOFO will be subject to terms and conditions found on the Award Conditions and Information for NIH Grants website. This includes any recent legislation and policy applicable to awards that is highlighted on this website.
Institutional Review Board or Independent Ethics Committee Approval: Recipient institutions must ensure that protocols are reviewed by their IRB or IEC. To help ensure the safety of participants enrolled in NIH-funded studies, the recipient must provide NIH copies of documents related to all major changes in the status of ongoing protocols.
2. Administrative and National Policy Requirements
All NIH grant and cooperative agreement awards include the NIH Grants Policy Statement as part of the NoA. For these terms of award, see the NIH Grants Policy Statement Part II: Terms and Conditions of NIH Grant Awards, Subpart A: General and Part II: Terms and Conditions of NIH Grant Awards, Subpart B: Terms and Conditions for Specific Types of Grants, Recipients, and Activities , including of note, but not limited to:
If a recipient is successful and receives a Notice of Award, in accepting the award, the recipient agrees that any activities under the award are subject to all provisions currently in effect or implemented during the period of the award, other Department regulations and policies in effect at the time of the award, and applicable statutory provisions.
Should the applicant organization successfully compete for an award, recipients of federal financial assistance (FFA) from HHS will be required to complete an HHS Assurance of Compliance form (HHS 690) in which the recipient agrees, as a condition of receiving the grant, to administer programs in compliance with federal civil rights laws that prohibit discrimination on the basis of race, color, national origin, age, sex and disability, and agreeing to comply with federal conscience laws, where applicable. This includes ensuring that entities take meaningful steps to provide meaningful access to persons with limited English proficiency; and ensuring effective communication with persons with disabilities. Where applicable, Title XI and Section 1557 prohibit discrimination on the basis of sexual orientation, and gender identity, The HHS Office for Civil Rights provides guidance on complying with civil rights laws enforced by HHS. See https://www.hhs.gov/civil-rights/for-providers/provider-obligations/index.html and https://www.hhs.gov/civil-rights/for-individuals/nondiscrimination/index.html .
HHS recognizes that research projects are often limited in scope for many reasons that are nondiscriminatory, such as the principal investigator’s scientific interest, funding limitations, recruitment requirements, and other considerations. Thus, criteria in research protocols that target or exclude certain populations are warranted where nondiscriminatory justifications establish that such criteria are appropriate with respect to the health or safety of the subjects, the scientific study design, or the purpose of the research. For additional guidance regarding how the provisions apply to NIH grant programs, please contact the Scientific/Research Contact that is identified in Section VII under Agency Contacts of this NOFO.
Please contact the HHS Office for Civil Rights for more information about obligations and prohibitions under federal civil rights laws at https://www.hhs.gov/ocr/about-us/contact-us/index.html or call 1-800-368-1019 or TDD 1-800-537-7697.
In accordance with the statutory provisions contained in Section 872 of the Duncan Hunter National Defense Authorization Act of Fiscal Year 2009 (Public Law 110-417), NIH awards will be subject to the Federal Awardee Performance and Integrity Information System (FAPIIS) requirements. FAPIIS requires Federal award making officials to review and consider information about an applicant in the designated integrity and performance system (currently FAPIIS) prior to making an award. An applicant, at its option, may review information in the designated integrity and performance systems accessible through FAPIIS and comment on any information about itself that a federal agency previously entered and is currently in FAPIIS. The Federal awarding agency will consider any comments by the applicant, in addition to other information in FAPIIS, in making a judgement about the applicant’s integrity, business ethics, and record of performance under Federal awards when completing the review of risk posed by applicants as described in 45 CFR Part 75.205 and 2 CFR Part 200.206 Federal awarding agency review of risk posed by applicants. This provision will apply to all NIH grants and cooperative agreements except fellowships.
3. Data Management and Sharing
Note: The NIH Policy for Data Management and Sharing is effective for due dates on or after January 25, 2023.
Consistent with the NIH Policy for Data Management and Sharing, when data management and sharing is applicable to the award, recipients will be required to adhere to the Data Management and Sharing requirements as outlined in the NIH Grants Policy Statement . Upon the approval of a Data Management and Sharing Plan, it is required for recipients to implement the plan as described.
4. Reporting
When multiple years are involved, recipients will be required to submit the Research Performance Progress Report (RPPR) annually and financial statements as required in the NIH Grants Policy Statement.
A final RPPR, invention statement, and the expenditure data portion of the Federal Financial Report are required for closeout of an award, as described in the NIH Grants Policy Statement . NIH NOFOs outline intended research goals and objectives. Post award, NIH will review and measure performance based on the details and outcomes that are shared within the RPPR, as described at 45 CFR Part 75.301 and 2 CFR Part 200.301.
The Federal Funding Accountability and Transparency Act of 2006 (Transparency Act), includes a requirement for recipients of Federal grants to report information about first-tier subawards and executive compensation under Federal assistance awards issued in FY2011 or later. All recipients of applicable NIH grants and cooperative agreements are required to report to the Federal Subaward Reporting System (FSRS) available at www.fsrs.gov on all subawards over $25,000. See the NIH Grants Policy Statement for additional information on this reporting requirement.
In accordance with the regulatory requirements provided at 45 CFR 75.113 and Appendix XII to 45 CFR Part 75, recipients that have currently active Federal grants, cooperative agreements, and procurement contracts from all Federal awarding agencies with a cumulative total value greater than $10,000,000 for any period of time during the period of performance of a Federal award, must report and maintain the currency of information reported in the System for Award Management (SAM) about civil, criminal, and administrative proceedings in connection with the award or performance of a Federal award that reached final disposition within the most recent five-year period. The recipient must also make semiannual disclosures regarding such proceedings. Proceedings information will be made publicly available in the designated integrity and performance system (currently FAPIIS). This is a statutory requirement under section 872 of Public Law 110-417, as amended (41 U.S.C. 2313). As required by section 3010 of Public Law 111-212, all information posted in the designated integrity and performance system on or after April 15, 2011, except past performance reviews required for Federal procurement contracts, will be publicly available. Full reporting requirements and procedures are found in Appendix XII to 45 CFR Part 75 and 2 CFR Part 200 Award Term and Conditions for Recipient Integrity and Performance Matters.
We encourage inquiries concerning this funding opportunity and welcome the opportunity to answer questions from potential applicants.
eRA Service Desk (Questions regarding ASSIST, eRA Commons, application errors and warnings, documenting system problems that threaten submission by the due date, and post-submission issues)
Finding Help Online: https://www.era.nih.gov/need-help (preferred method of contact) Telephone: 301-402-7469 or 866-504-9552 (Toll Free)
General Grants Information (Questions regarding application instructions, application processes, and NIH grant resources) Email: [email protected] (preferred method of contact) Telephone: 301-480-7075
Grants.gov Customer Support (Questions regarding Grants.gov registration and Workspace) Contact Center Telephone: 800-518-4726 Email: [email protected]
Marsha F. Lopez, Ph.D., M.H.S. National Institute on Drug Abuse (NIDA) Telephone: 301-443-6504 Email: [email protected]
Keisher Highsmith, Ph.D. National Institute on Drug Abuse (NIDA) Telephone: 301-402-1984 Email: [email protected]
Guifang Lao, M.D., Ph.D. National Institute on Drug Abuse (NIDA) Telephone: 301-827-5931 Email: [email protected]
Beth Babecki, M.A. National Institute on Drug Abuse (NIDA) Telephone: 301-435-0899 Email: [email protected] Lindsey Friend, Ph.D. National Institute on Drug Abuse (NIDA) Telephone: 301-402-1428 Email: [email protected]
Examine your eRA Commons account for review assignment and contact information (information appears two weeks after the submission due date).
Ericka Wells National Institute on Drug Abuse (NIDA) Telephone: 301-827-6705 Email: [email protected]
Recently issued trans-NIH policy notices may affect your application submission. A full list of policy notices published by NIH is provided in the NIH Guide for Grants and Contracts . All awards are subject to the terms and conditions, cost principles, and other considerations described in the NIH Grants Policy Statement .
Awards are made under the authorization of Sections 301 and 405 of the Public Health Service Act as amended (42 USC 241 and 284) and under Federal Regulations 42 CFR Part 52 and 45 CFR Part 75 and 2 CFR Part 200.
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Your kidneys could be damaged if you take large amounts of over-the-counter medications, such as aspirin, naproxen and ibuprofen. None of these medicines should be taken daily or regularly without first talking to your healthcare provider. Thousands of Americans have damaged their kidneys by using these medicines regularly for too long. To learn more about pain medications and your kidneys click here .
Heavy drinking can hurt both your kidneys and your liver. Alcoholics have a high risk of developing both kidney and liver failure. Learn more about alcohol and your kidneys .
Antibiotics can also be dangerous if they are not taken correctly. People with kidney disease need to take a smaller amount of antibiotics than people with healthy kidneys. Take only medicines ordered for you by your healthcare provider.
In general, over-the-counter laxatives are safe for most people. However, some prescription laxatives that are used for cleaning the bowel (usually before a colonoscopy) can be harmful to the kidneys. To learn more click here .
Some medical tests called "imaging tests" contain a type of dye called "contrast dye." Examples of imaging tests are MRIs and CT-scans. Contrast dyes can be harmful to people who have kidney disease. Not all imaging tests contain contrast dyes. To learn more about contrast dye click here .
Most street drugs, including heroin, cocaine and ecstasy can cause high blood pressure, stroke, heart failure and even death, in some cases from only one use. Cocaine, heroin and amphetamines also can cause kidney damage.
Related kidney topics, six easy ways to prevent kidney stones, nutrition and hemodialysis, percutaneous nephrolithotomy / nephrolithotripsy, sodium-glucose cotransporter-2 (sglt2) inhibitors, dialysis: dry, itchy skin, related news and stories.
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More than half of Arkansans using medical marijuana in 2021 used the drug as a pain reliever, and a large proportion of patients have used it to treat post-traumatic stress disorder, according to study findings presented to state lawmakers Wednesday.
The study, conducted by the Arkansas Center for Health Improvement, is the first ever population-based study of medical marijuana funded by a federal health agency, the National Institutes of Health.
As of this month, more than 3% of Arkansas adults have received permission from physicians to use the drug to treat one or more of the state’s 18 qualifying medical conditions . The state currently has more than 105,000 cardholders, an increase of roughly 29,000 in three years, according to ACHI’s study.
Thompson said ACHI is seeking another federal grant to do further research on medical marijuana use, including rates of substance use disorder among users.
“There’s been very little clinical research because there’s no federal money flowing for clinical research, so we don’t really know much about marijuana other than anecdotal reports and small studies,” Thompson said.
Arkansans voted to legalize cannabis for medicinal use via a constitutional amendment in 2016, though the first products were not sold until 2019. Five years later, medical marijuana has grown to be a billion-dollar industry with 37 dispensaries throughout Arkansas.
Marijuana is federally illegal because it is classified as a Schedule I controlled substance. The Drug Enforcement Administration has recommended that the Department of Justice reclassify it to Schedule III, the category for regulated but legal substances.
Thirty-eight states and the District of Columbia have legalized marijuana to some extent, and Arkansas is one of 14 states in which the drug is legal only for medicinal purposes.
Physicians are not allowed to prescribe specific amounts or dosages of marijuana because of its current federal status compared to other drugs, said committee co-chair Sen. Missy Irvin, R-Mountain View, in response to some lawmakers’ questions.
Cardholders visit dispensaries every 11 days on average, and the amount of product sold daily “far exceeds existing clinical recommendations” for consumption, according to the report.
All dispensaries are required to have consultant pharmacists who can provide advice on the distribution of marijuana, but most of them work remotely, and several facilities employ the same few pharmacists, Thompson said.
The study relied on a variety of data sources, including the state medical board’s licensure database and the All-Payer Claims Database, which tracks “how and where healthcare is being delivered and how much is being spent,” according to its website .
The APCD showed that in 2021, about 92% of medical marijuana cardholders had seen a physician in the previous year, and 62% had seen a physician regarding a diagnosed condition that they used medical marijuana to treat, the report states.
The study examined the clinical impact of medical marijuana on conditions it is frequently used to treat, and data showed that there was no significant difference in prescription medication use for PTSD patients whether they did or didn’t use medical marijuana, according to the report. However, non-users of medical marijuana were hospitalized more frequently for PTSD symptoms than those who used the drug for the illness.
Researchers have not found proof that medical marijuana use plays a role in the opioid epidemic, Thompson said in response to a question from Sen. Fred Love, D-Mabelvale.
Thompson gave the committee several policy recommendations from the results of the study, such as strengthening the requirements to prove physicians’ relationships with the patients they are certifying for a medical marijuana card, altering purchase limits based on consumption recommendations and creating stronger enforcement policies to discourage users from giving away or selling unconsumed products.
Rep. Zack Gramlich, R-Fort Smith, said he was concerned that the growth of the medical marijuana industry might unintentionally give children access to marijuana products. Medical marijuana cardholders must be at least 18 years old.
“Kids who would never normally be around this stuff are now getting connected to it,” said Gramlich, citing his experience teaching middle school.
Thompson said he was aware of the “real challenge” parents and educators face trying to keep children away from controlled substances but was not aware of any existing ways the state can identify which medical marijuana cardholders have children.
Sen. Linda Chesterfield, D-Little Rock, said she wanted more state oversight of the medical marijuana industry to confirm that “from seed to sale, we are making sure that the product is a good product.”
She also said she was more concerned about “the industry itself” and dispensaries being managed by very few people despite there being dozens of facilities and owners throughout the state.
A Little Rock law firm was sued last year in Pope and St. Francis counties over fraud and legal malpractice claims regarding the creation of ownership groups to obtain four of the state’s first 32 dispensary licenses in 2019. The defendants responded with a defamation lawsuit in Pulaski County Circuit Court. Both cases are still pending.
Arkansas Advocate is part of States Newsroom, a nonprofit news network supported by grants and a coalition of donors as a 501c(3) public charity. Arkansas Advocate maintains editorial independence. Contact Editor Sonny Albarado for questions: [email protected] . Follow Arkansas Advocate on Facebook and X .
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When you buy soaps and body washes, do you reach for products labeled “antibacterial” hoping they’ll keep your family safer? Do you think those products will lower your risk of getting sick, spreading germs or being infected?
According to the U.S. Food and Drug Administration, there isn’t evidence to show that over-the-counter (OTC) antibacterial soaps are better at preventing illness than washing with plain soap and water. In fact, some data suggest that antibacterial ingredients could do more harm than good over the long-term.
“Following simple handwashing practices is one of the most effective ways to prevent the spread of many types of infection and illness at home, at school and elsewhere,” says Theresa M. Michele, M.D., of the FDA. “We can’t advise this enough. It’s simple, and it works.”
The FDA issued a final rule in 2016 under which most antibacterial active ingredients, including triclosan and triclocarban, can no longer be marketed in nonprescription consumer antiseptic wash products. Those products include liquid, foam and gel hand soaps; bar soaps; and body washes.
The FDA made this determination because manufacturers didn’t prove that those ingredients are safe for daily use over a long period of time. Also, the manufacturers didn’t prove that those ingredients are any more effective than plain soap and water in preventing illnesses and the spread of certain infections.
The FDA’s rule doesn’t apply to three ingredients: benzalkonium chloride, benzethonium chloride and chloroxylenol. Manufacturers are developing and planning to submit new safety and effectiveness data for these ingredients.
The FDA’s final rule covers only consumer antibacterial soaps and body washes that are used with water. It does not apply to hand sanitizers , hand wipes or antibacterial soaps used in health care settings, such as hospitals and nursing homes. To learn about the difference between consumer hand sanitizers and consumer antibacterial soaps, visit the FDA’s webpage on this topic.
Antibacterial soaps (sometimes called antimicrobial or antiseptic soaps) contain certain chemicals not found in plain soaps. Those ingredients are added to many consumer products with the intent of reducing or preventing bacterial infection.
“There’s no data demonstrating that these drugs provide additional protection from diseases and infections. Using these products might give people a false sense of security,” Michele says. “If you use these products because you think they protect you more than soap and water, that’s not correct. If you use them because of how they feel, there are many other products that have similar formulations but won’t expose your family to unnecessary chemicals.”
How do you tell if a product is antibacterial? For nonprescription drugs, antibacterial products generally have the word “antibacterial” on the label. Also, a Drug Facts label on a soap or body wash is a sign a product contains antibacterial ingredients.
What should consumers do? Wash your hands with plain soap and water.
Washing your hands is easy , and it’s one of the most effective ways to prevent the spread of germs.
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Student research journal, drug use in relation to popular culture, media and identity.
The objective of this study is to examine the extent to which representations of drug use within popular culture and media, are impacting an individual’s identity within contemporary society. This concept has been vastly under-researched and theories, as well as drug normalisation in terms of an individual’s identity, making this research tremendously invaluable as it to give a rigorous investigation in a modern setting.
Through the use of secondary data collection methods, this research has investigated the positive perception of drug consumption displayed in music, and the honest insights displayed in television and cinema; it has highlighted the usefulness of social media to individuals looking to create their own realities surrounding drug consumption in comparison the mass media that creates moral panics and fear. The research revealed that drug representation trends in both popular culture and media are perennial and impact an individual’s identity differently. For example, fans of punk music during the 1970s cultivated the amphetamine look to fit into the social group surrounding this genre of music, even though they might not have experimented with amphetamine itself, whereas the media created a moral panic around mephedrone in which they and society used drug users as social pariahs.
Author: Olivia Mackay, April 2020
BA (Hons) Criminology with Forensic Science
Firstly, I would like personally thank Kay Brady for her expert knowledge and continual support throughout this academic year, and the composing of this dissertation paper.
“When we think about drugs, we may draw upon our own experiences or the knowledge and understanding of those close to us, but our experience is always intimately bound up with, or tempered by, the mediated images and in ideas about drugs that circulate through wider popular culture”, (Manning, 2013: 8).
This dissertation is about the depiction of drug consumption in popular culture and media, and how this is directly affecting an individual’s identity; popular culture shall relate to music, television, and cinema while media will relate to mass and social media.
Although defining the term can be considered difficult, the term ‘drug’ can be defined as a ‘single substance that, when ingested, produces a physiological effect, pharmacological effect, or change’, (Bell, 2012: 74). Gossop (2007) offers a slightly different definition, stating it to be ‘”any chemical substance, whether of natural or synthetic origin, which can be used to alter perception, mood or other psychological states”, (Gossop, 2007: 2). Furthermore, recreational drug use can be defined as the ‘use of drugs for pleasure or leisure’, (DrugScope, 2014); this is frequently mentioned throughout this dissertation. Drug use is something that has always been associated with distinct youth culture movements; in terms of popular culture, these movements included the ‘speeding mods’ on the 1960s whereby drug experimentation focused on amphetamines, ‘hippies’ throughout the 1970s and LSD consumption and heroin users throughout the 1980s.
This was of course picked up on by the media, who have waged a ‘war on drugs’ throughout the decades. Boyd (2002) highlighting that this trend is perennial stating that since the mid-1800s, media representations of drugs users and traffickers have centrered on what is perceived as the ‘dangerous classes’, that threaten white, middle-class protestant morality, (Boyd, 2002: 397).
I decided to do this piece of work as I find the topic of drug use in contemporary society academically interesting. The idea that the representation of drug consumption in the media and popular culture can affect someone’s social identity is vastly under-researched and theorised, which makes this piece of work vital in understanding that there are direct links and correlations. Consequently, the hypothesis is ‘the representation of drugs in popular culture and media will have consequences on an individual’s identity in contemporary society’. The core research question to be tested for this dissertation is ‘how drug use is presented within popular culture and media, and how this can affect an individual’s identity’.
One of the aims of this dissertation is to conclude whether listening to specific genres of music, corresponds to drug consumption or drug experimentation. The second aim is to highlight whether popular culture is seen to offer a positive perception of poly-drug use in contrast to social and mass media and whether this causes a moral panic. The overall objective is to emphasise whether trends in popular culture and media are perennial; therefore, popular culture and mass media will not differ from the pre-conceived ideas set out historically, and how this ultimately affects the individual in contemporary society.
Chapters within this dissertation include a methodology section, literature-based discussion and a conclusion. The methodology section will primarily focus upon the research methodology and summarize the research technique. It shall take note of the advantages and disadvantages of both a literature-based discussion and secondary data collection. Lastly, it will address any ethical issues encountered during the writing of this dissertation. The second section will provide a comprehensive view of the existing literature that is relevant to popular culture, media, and identity. It will provide an in-depth analysis of the emergence of drug imagery in mainstream popular culture and media, bringing forward the normalisation and social identity concepts using fundamental case studies such as Leah Betts and mephedrone. The conclusion section shall draw together all the findings from the literature-based discussion, striving to support the research hypothesis.
I decided to do a literature-based dissertation as I believed this topic to be vastly under-researched and theorised; it became relevant to combine pre-existing literature and to bring this into a more contemporary setting. Furthermore, I really wanted to study this topic and to be able to do this ethically, at an undergraduate level, it was necessary to use secondary data collection methods over that of primary data methods. This was necessary as trying to collect primary data could implicate the dissertation ethically, (this is something touched upon during the ethical considerations).
Secondary Data is classified as “the act of collecting or analysing data that was originally collected for another purpose”, (Bachman et al., 2011: 306). Secondary data allows for examination of already accessible material based on the speculations and acknowledgments within this research area; it will utilise core texts such as books, websites, journal articles and newspaper articles. Core texts, such as books, can be useful as they explain the pre-
existing data and acknowledge the relevant arguments that may be pertinent to today’s society. Journal articles offer the researcher a view of late modernity and websites and newspaper articles can note relevant and contemporary changes; these also tend to offer a personal view of the study.
One benefit of collecting secondary data is that it gives this dissertation access to a plethora of resources that have already been accumulated. This method allows from the use of a substantial scale of data which I believe could not have been replicated by an undergraduate student within the set time sale. It gives this dissertation access to more meticulous data evaluations, making it easier to submit findings and correlations between pre-existing data and theories.
However, it must be mentioned that secondary data has potential limitations. At the original time of this data being collected and created, the researcher has decided upon a subject of interest which could inadvertently lead to bias or a subjective outcome; this means that I can become hard to clarify whether the data collected was accurate. Both newspaper articles and journal articles can lead to a misrepresentation of results through tabloid political and ideological bias. Furtherance of this, what is known as the ‘dubious value’, when attempting to pinpoint the levels of crime in society, serves to highlight that there is a lack of understanding; this has become the ‘dark figure of crime’.
This dissertation does not include primary data and is solely based on academic material that was available as the University of Hull’s, Brynmor Jones Library. Any and all online sources where accessed through Google Scholar. Keyword searches were utilised and refined to ensure that sources found were both disparate and relevant to the key question; sources that fitted both these criteria where contemplated for inclusion.
The most prominent ethical consideration that was made whilst planning this dissertation is attributed to the collection of primary data. The original idea for the dissertation focused on drug normalisation within university students, with primary data being accumulated through the use of interviews and surveys from students across the country. It strived to look at the differing drug use depending on the attending university, and the course undertook by the student. However, in doing so, individuals would have implicated themselves and risked confessing to illicit drug consumption and experimentation, thus disclosing illegal behaviour. According to the ethics policy published by the University of Hull, “research involving human participants must consider the impact/s of the research on the participants. This includes direct, indirect and broader impacts (for example, impact(s) on their family, society, employers or colleagues), (Research Ethics Policy, 2017: 9). This means that the research being conducted for this dissertation should not impact the individual, which admitting to illicit drug consumption (whether anonymous or not) had the potential of achieving.
This literature-based discussion will critically analyse the surrounding literature regarding the representation of drug use within popular culture and media, and how this can have an impact on an individual’s identity; it shall be separated into sectioned to guarantee that there is precise assessment and simplicity surrounding the key themes and arguments. The first segment intends to investigate popular culture and include themes such as music, television, and cinema. The theme of music shall explore the changing representations of drugs and drug consumption, referencing influential musicians such as Johnny Rotten and The Beatles. It will also discuss statistics surrounding music genre preference and drug consumption and experimentation rates. The theme of television and cinema shall explore the negative portrayal of drug use that is portrayed in British television dramas, Shameless and Ideal, as well as popular Scottish film, Trainspotting.
The second section will discuss both mass and social media, bringing forward theorists such as Ben-Yehuda and Kohn, who highlight the false reality of media representations. It will critically analyse the mephedrone epidemic of 2009/2010 and the death of Leah Betts, paying particular attention to, The Sun newspaper’s contribution to the moral panic that ensued. When discussing social media, the contemporary studies by both Cavazos-Rehg and colleagues (2014) and Hanson and colleagues (2013a) will be drawn upon to support the idea that social media enables the user to create their own media and realities, that allow for positive perceptions of poly-drug use.
The final section will reference identity. This will discuss the normalisation thesis, creating links to the first two sections of popular culture and media. The social identity theory, which was documented by Tajfel and Turner (1979), will also be utilised to aid in critically analysing whether popular culture and media do indeed have a direct correlation to an individual’s social identity and stance on drug experimentation.
Popular culture is arguably one of the most influential sources for positive perceptions of poly-drug use; it is noted that both illicit and licit drug use has continuously been considered lived elements within popular culture, therefore providing substantial concepts for popular culture literature. Blackman (1996) support this notion, stating that “one of the visible links between youth culture and drug culture is the visible display of youth styles; it is possible to argue that there exists a repository of ideas and images in popular youth culture which are drug-influenced, (Blackman, 1996: 139). This gives the view that both drug consumption and popular culture, (and their mediations through society), are of some importance; for example, the distinction between both licit and illicit is maintained through definitions that are politically, but more importantly, socially administered. Before delving into this research, it is important to note (as Oksanen, 2012 does) that the recent body of research surrounding popular music and drug use is virtually non-existent; a large section of contemporary literature has concentrated on rave and techno club music. Thus, the data may be skewed, (Oksanen, 2012: 143).
Beginning firstly with the notion that music inspires drug consumption, preceding the 1990s, recreational drug experimentation was vastly viewed as a marginal activity. Beginning firstly with the notion that music inspired drug consumption, prior to the 1990s, recreational drug experimentation was vastly regarded as a marginal activity; Shapiro (1999) remarking that those who took part in such activities were to be branded as ‘mad, bad or sad’, (Shapiro, 1999: 17). Looking at contemporary society, Brian and Measham (2005) point to a new culture of inebriation whereby both illicit substances and alcohol are at the forefront, (Manning, 2007: 3). It can be speculated that the relationship between drug consumption and music is perennial, with each coming decade offering a new music genre coupled with a novel, ‘fashionable’ drug to experiment with. This is exemplified in the role of a reefer (a cannabis cigarette) within jazz and blues in the early twentieth century, as well as amphetamines and hallucinogens at the close of the century with dance and rave music. From this, it can be maintained that popular music appears to offer listeners the possibility, real or imagined, to share the drug experiences with the cultural producers, meaning that these pleasures are considered a ‘secret’ between performers and fans. Andrew Blake touches on this, commenting that pop music has been central in the construction and rotation of symbolic frameworks that ‘make sense’ of drugs and drug consumption, (Manning, 2007: 101). Popular music has arguably offered the most extensive cultural space within which drug pleasures and experiences can be globally represented; these energies and opportunities for drug experimentation in musical form have found a parallel in the willingness of famous musicians to experiment with drugs.
A prime example of this comes from The Beatles, whose careers survived and flourished on drugs such as Drinamyl and Preludin (a stimulant drug, previously used as an appetite suppressant); this drug trend spread from the band to the fans, (Normal, 1992: 98 cited in Shapiro, 2000: 20). Drugs, for the most part, provided The Beatles with a means of escape and distraction from being in the public eye; they openly discussed their drug consumption, arguing that they never wanted their fans to mimic their actions. Gooddens (2017) quotes John Lennon, who, in 1970 said, “I do not lead my life to affect other people”; a year adding “I do not feel responsible for turning [fans] onto acid. Because I do not think we did anything to kids; anything someone does, they do themselves” (Gooddens, 2017: ND). This suggests that musicians realise the promotion of drug consumption is replicating onto individuals, however they perceive it to be an individual’s choice not because of their influence.
The representation of drug consumption continued with the emergence of a new club culture termed ‘mod’. Bands such as The Who, and Small Faces, began to express the amphetamine style both lyrically and stylistically. Shapiro (2000) exemplifies Roger Daltrey, lead singer of The Who, who punctuated the popular song ‘My Generation’ with the amphetamine stutter – something which is considered typical of a user who had great difficulty getting their words out fast enough. Furthermore, Small Faces explicitly mentioned ‘speed’ and ‘itchycoo park’ (rumoured to be an explicit reference to amphetamine formulation) during their performance of ‘Here Comes the Nice’ on Top of the Pops, (Shapiro, 2000: 20). This amphetamine culture became prominent, during the 1970s Punk era and thus had a more profound impact. During this period, the commodification of punk and rock genres of music had increased alongside its cultural respectability. Shapiro (2000) exemplified Johnny Rotten, lead singer of the Sex Pistols, who can be considered a prominent drug figure during this period. Rotten gained his renowned stage name from the state of his rotten teeth; he became so influential to the punk style and scene, that many adolescents that followed punk music, attempted to cultivate his amphetamine look, without partaking in drug use, (Shapiro, 2000: 27). This highlights that the ‘drug look’ became favourable among fans because they wanted to convey a particular identity or fit into a specific social group.
Shapiro (2000) further relates this to contemporary society and the rise of the dance culture that came from Ibiza. This new dance culture, which is based on the sounds of house and garage, sprang up in the UK with many DJ’s looking to recreate the ‘sounds of the summer’; this led to the emergence of MDMA. Shapiro (2000) continues with this, stating that these critical developments in popular music, and the catalytic appearance of ecstasy, combined to create a unique symbiosis, heralding the normalisation of illicit drug use, (Shapiro, 2000: 18). This suggests that lyrically and stylistically, the positive representation of drug experimentation and consumption is deeply rooted in music and can be considered perennial.
This directly links to the notion that listening to specific genres of music positively correlates to drug consumption. Lewis (1980) conducted a survey in which 2,950 16-year-olds were asked who their favourite recording artist was and several questions concerning drug usage; he found that heavy metal listeners were more likely to engage in drug experimentation (across all categories of drugs) compared to other genres such as Jazz, Rock & Roll, and Disco-Dance. For example, out of 831 heavy metal listeners, 275 frequently smoked marijuana in comparison to 88 for Rock & Roll, and 39 for Disco-Dance; another example shows that, again out of 831 heavy metal listeners, 53 frequently took stimulants over that of 6 for Jazz and 1 for country music. This trend is mimicked across other categories of drugs such as cocaine, PCP, tranquillizers, inhalants and opiates, (Lewis, 1980: 176 – 179). Furtherance of this, Lewis draws upon the Youth in Transition Survey (1970), which focused on 19-year-old males. Robinson found a slight correlation between individuals with a preference for protest rock and self-reported drug consumption; he found that protest rock and drug consumption was the strongest for marijuana and hallucinogens and weaker with amphetamine and barbiturates. However, it must be noted that Robinson believed that this was more to do with peer group usage over the positive representation of drug consumption by the musicians.
Another popular culture source comes from television and cinema, which are seen to offer negative but normal views of drug consumption, with shows such as, The Mighty Boosh, and Shameless, depicting marijuana as a normal part of everyday lives. Manning (2007) firstly draws attention to popular British television drama Shameless, which is seen to portray a picture of normalised, but illegal, recreational drug use – something which is not far removed from the everyday lived realities of many young, ordinary people in the UK, (Manning, 2007: 1). The main character, Lip, is seen ordering a pint of lager, a whiskey chaser and an ‘E’ (ecstasy), to relieve himself of relationship drama; this specific scene offers the audience the idea that poly-drug use can be routine. Whilst customers may not be able to buy illicit drug substances over the bar, drugs are quite likely to be on sale somewhere close by. This normalised image is supported by the television programme, Ideal. Carter (2007) believes that, Ideal was an important development in British television broadcasting as it was the first sit-com to have a drug-dealer as a main character while acknowledging the illegality and making drug dealing appear as unglamorous as possible, (Carter, 2007: 169).
The risks of the show, overall, appear severely mediated by the attempts to show the life of a drug dealer as unattractive and squalid.
A prominent film is the Scottish, Trainspotting, which despite being about a group of heroin users, became popular across Britain; its 1996 release coming at a pivotal time for the British drug culture. Trainspotting follows a group of young Scottish heroin users during the late 1980s in Edinburgh, Scotland; the narration is done by that of the protagonist, Mark Renton, who is a self-proclaimed heroin addict. Throughout the film, Renton goes through periods of being both on and off heroin, which seemingly corresponds with the highs and lows of Renton’s life; throughout these periods of heroin use and withdrawal, the audience is shown the image of a heroin addict, with Renton’s narration offering insight into the attitude of a heavy user and their mentality. Director, Danny Boyle, comments on his representation of drug use throughout the film, stating:
“This isn’t what drugs are about. When you take drugs, you have a [expletive] time – unless you’re very unlucky. We wanted the film to capture that. There’s half of the film which is considerably darker. If you prolong the experience with drugs, your life will darken. The film doesn’t try and hide that. But it also doesn’t try to hobble along with the moral consensus” (Byrne, 1997: 173).
This quote highlights that film is attempting to show an honest view of drug use and what prolonged us (addiction) can so to someone. Overall, the film fits the notion that cinema and television offer a negative view of drug use in comparison to other forms of popular culture. This is evident through the fact that Renton’s values and convictions surrounding life and heroin use conflict with the overarching message of the film; the dual messages of Renton’s rocky relationship with heroin serves to challenge the popular notions of heroin addiction.
For the majority of people in contemporary society, primary exposure to drug consumption derives from mainstream media outlets such as newspapers and region-specific television broadcasts. Manning (2007) cites the work of Jenkins, who observes that the perennial public scepticism concerning the lurid drug scare, circulates mainstream media outlets because an increasing portion of the news audience has either direct or indirect exposure to drugs, (Manning, 2007: 8). Ben-Yehuda (1994) builds from this, remarking that the representation of the drug ‘problem’ by such media outlets bears little resemblance to the reality of the situation, (Ben-Yehuda, 1994: 200). This suggests that, although the audience may have the knowledge or lived experience of drug use, media outlets still portray it in a distorted way with a potential outcome of a moral panic. Kohn supports this, arguing that how mass media represents the drug ‘problem’ in the UK, is nothing more than an attempt to divert attention away from other burgeoning issues such as high unemployment and poverty, (Ben-Yehuda, 1994: 200). Boland (2000) notes that these views on drug consumption are embedded in the public mindset; therefore, the media can use drug users like social pariahs that can be blamed for today’s social ills, (Boland, 2000: 173); this leads to individuals in society doing the same. However, Manning (2007) comments that the suggestion that mainstream media outlets play an essential role in the identification, definition, and construction of social problems is not new. Mainstream media outlets have long played an essential part in the differentiation of patterns of intoxication and what is deemed ‘appropriate’ and ‘inappropriate’ drug use (Manning, 2007: ND).
The most prominent feature of mass media that surrounds drug use is moral panics; Cohen
(1971) conceptualised moral panics and folk devils, stating:
“Societies appear to be subject, now and then, to periods of moral panic. A condition, episode, person or group of persons emerge to come defined as a threat to societal values and interests, its nature is presented in a stylised and stereotypical fashion by the mass media; the moral barricades are manned by editors, bishops, politicians and other right-thinking people … Sometimes the object of the panic is entirely novel, and at other times it is something which has been in existence long enough, but suddenly appears in the limelight.” (Marsh et al., 2011: 2)
This is supported by Goode (2017) who highlights that a moral panic is an intense and heightened sense of exaggerated concern about a threat, or supposed threat, posed by deviants or ‘folk devils’, (Goode, 2017: 149). Jewkes and colleagues (2005), depict moral panics as events that occur randomly and provoke an extreme reaction, (Jewkes et al¸ 2005: 22). Beginning to relate this to contemporary society, Thompson (1998) regards that the new decade is the age of moral panics, stating that tabloid headlines are continually warning society of new dangers that result in moral laxity; however, Thompson continues by stating that moral panics are not a new concept as there has been a multitude of moral panics over issues such as crime and youth activities, (Thompson, 1998: 1). Young (1971a) highlights that within these moral panics, mass media can create ‘fantasy notions’ around drug takers and the consequences of deviancy amplification. Furtherance of this, Murji (1998) persuasively argues that:
“The dominant, conventional approach has seen the media as a key force in the demonisation and marginalisation of drug users, as presenting lurid, hysterical images and as a provider of an un-critical platform from which politicians and other moral entrepreneurs can launch and wage drug ‘wars’. The media is thus seen to comprehensively misrepresent drugs, their effects, typical users and sellers … In many ways, the media may even define what we ‘see’ as drugs … thereby conditioning public attitudes about the ‘drug problem’ and what the response to it should be”. (Murji, 1998: 69)
This serves to highlight that due to the media negative image of drug consumption being so prominent, high-ranking members of society are able to control information given to the public – a lot of said information being false or distorted.
These ‘fantasy notions’ surrounding drug moral panics creates what is known as outsiders. Taylor (2008) conveys that the negative and, quite frankly, stereotypical depictions of drug users by the media, creates criminal outsiders that are a threat to middle-class sobriety, (Taylor, 2008: 370). This is supported by Peretti-Watel (2003), who emphasised the importance of the aforementioned ‘folk devil’ stereotype, using the publics pre-conceived notions of heroin users as a prime example. For instance, Peretti-Watel stresses that the media’s depiction of heroin users is that of devils that concentrate all types of vices (Peretti-Watel, 2003: 322). This has links to Becker’s (1963) illustration of drug users being framed as ‘others’ and presented as a risk to ‘us’ as a society.
Boyd (2002) supports the idea, noting that these perceptions created by the media are indeed perennial. He relates this to the USA, but these themes are equally tenable to the UK:
“Since the mid-1800s, media representations of drug users and traffickers in the US have centred on what is perceived as the ‘dangerous classes’ and racial minorities as the ‘other’. Drug traffickers are constructed as the ‘outsiders’ that threaten the world order of white, middle-class protestant morality. They are depicted as dangerous, out of control, and a threat to the nation and the family. Today’s war on drugs is characterised by the ‘routinisation of caricature’ which promotes worst-case scenarios as the norm, sensationalises, and distorts drug issues in the media’, (Boyd, 2002: 397).
This quote serves to highlight that between the 1800s and today’s society, the image of drug users and traffickers represented in the media hasn’t differed from the ‘dangerous thug’ that risks being a detriment to societies morality.
However, there are a plethora of criticisms attributed to moral panics that must be observed. Firstly, the formulation of moral panics implies that the media’s audience is passive; however, audiences today are considered much more active and are able to critically evaluate media content; this may be due to the rise of social media as a different source of news. Additionally, Sparks (1992) notes that the term ‘moral panic’ can be overused to such as extent that society risk reducing this period of late modernity to an endlessly cyclical state of ‘pickiness’, (Sparks, 1992: 65). Taylor (2005) supports this believing that moral panics are nothing more than a ‘simmering’ panic than a moral one. Moreover, Thornton (1995) found that the media failed to produce a moral panic over the rave culture as this culture, and taking drugs such as ecstasy, had become mainstream and ‘normal’.
An excellent case study that shows how the media negatively portrays illicit substances and creates moral panics is that of mephedrone. Mephedrone, also known as 4-methylmethcathinone, is a central nervous system stimulant that is structurally similar to amphetamine, (Kari et al., 2011: 2). Presently, there are no pharmacokinetic or pharmacodynamic studies concerning mephedrone, nor are there any psychological or behavioural studies which asses the effects on humans; any reported psychological or behavioural effects of mephedrone are based on user reports as well as clinical reports on the toxicity of mephedrone, (Pistos et al., 2011: 192). This means that any media-generated human effects are cultivated to produce fear and does not stem from scientific research.
In 2009, mephedrone was at the forefront of public agenda after the tabloid newspaper, The Sun, published a fake report under the headline ‘Legal drug teen ripped his scrotum off’; this story had been initially published as a joke on an online forum and later quoted in a police report. This was information The Sun had failed to include (Kari et al., 2011: 3). Before the general election in 2010, the purportedly innocuous drug had the attention of the general public and politicians as the leading media outlets called for an immediate ban on the substance. The Sun, one of the aforementioned leading media outlets, launched an open campaign in which they demanded action from the government whilst simultaneously dismissing statements to wait on advice from the Advisory Council on the Misuse of Drugs; this instigated weeks of media debate regarding mephedrone, (Kari et al., 2011: 4).
During the campaign, The Sun reported that an 18-year-old and 19-year-old had died whilst under the influence of mephedrone; it was only speculated that mephedrone played a part in the deaths of both these boys. Toxicology reports state that mephedrone was not present.
However, the drug had already been framed by the media as dangerous, and the emotively reported deaths of these young adults had narrowed the possibility for an open and frank discussion about the actual harm of mephedrone, and the best policy options to be implemented.
Petley and collaborators (2013) exemplify the death of 14-year-old girl, Gabi Price, who also gained widespread media coverage. Tabloid papers reported that Price had taken mephedrone alongside ketamine, later dying of heart failure; it was further testified by the pathologist report that Price had died of natural causes following pneumonia from heart failure. Petley believes that stories such as these allow moral panics to ‘construct a discourse of information’ in which deaths are misattributed to drug consumption and the ‘real’ causes are ignored, (Petley et al., 2013: 126). This suggestion was supported by David Nutt (2010), who was the former chairman of the UK’s Advisory Council on the Misuse of Drugs; he stated that the knee-jerk policy change that was implemented, only served to highlight the ongoing tensions between “the causes of evidence-based policymaking and the imperative of headline-driven politics”, (Kari et al., 2011: 1). Overall, this case study supports the previous arguments surrounding moral panics as mephedrone was represented as a ‘threat to societal values or interests’, (Cohn, 2002: 1, cited in Petley et al., 2013: 127). It clearly shows how mainstream right-wing British media framed mephedrone as a moral epidemic and a ‘killer of youth’, perpetuating the traditional war on drugs rhetoric. Alexandrescu (2013) uses Van Dijk’s (1998, 2005, 2009) socio-cognitive model to explain that this ‘war on drugs’ rhetoric illustrates ideological discourses that derive from social elites, aiding in their domination because they can structure cognitive maps of social universes and shape the social context in which they are decoded, (Alexandrescu, 2013: 27). This suggests that tabloid newspapers were using their position of power and the growing ‘War on Drugs’ rhetoric to dominate an individual’s views and morals.
Another example of the media’s distorted and negative portrayal of drug consumption comes from the death of Leah Betts. Betts was an 18-year-old schoolgirl from Latchingdon, Essex, who on the 11th November 1995, took MDMA and drank seven litres of water in 90 minutes. Four hours later, Leah Betts collapsed into a coma from which she never recovered. This received extended media coverage from the time it occurred, through to her funeral and over two months later when the inquest returned a verdict of accidental death, (Murji, 1998: 71). During the peak of media attention, the aforementioned newspaper, The Sun, gave its front page to the story with the headline ‘Leah took ecstasy on her 18th Birthday’ and a full-page photograph of her lying on a hospital bed with a respirator on her face. Osgerby (1998) notes that, for the media, Leah’s death was a ‘potent image of innocence corrupted by a dangerous and malevolent subculture’, (Osgerby, 1998: 183). After Leah’s death, the media began to focus on the putative fact that it was the first time Betts had taken the drug; however, it arose later that she had taken ecstasy at least three times previously – although this was much less publicised.
In terms of this case study supporting the idea that the media creates drug moral panics, Cohn noted that psychoactive drugs had been a remarkably consistent source of moral panics, using the reaction to the ecstasy-related death of Leah Betts as a ‘melodramatic example’; Cohn argues that Leah’s death had been ‘symbolically sharpened’ by her ‘respectable home background: father an ex-police officer, mother had worked as a drug counsellor … Leah was the girl next door”, (Cohn, 2002: xiii, cited in Shiner et al., 2015: 1)
Thanki and colleagues (2016) define social media as encompassing numerous types of social interaction applications and sites, including social networking sites, photo and video-sharing sites, blogs and microblogs, discussion and forum sites, review and rating sites and social streams, (Thanki et al., 2016: 115).
Cavazos-Rehg and colleagues (2014) analysed demographics of almost 1 million followers of pro-marijuana Twitter handle as well as the content under that handle. They found that 73% of followers were 19-year-olds or under, with 54% being female. Furthermore, they found that content posted, mainly concerned positive cannabis discourse, with many being perceived as humorous, (Thanki et al., 2016: 117).
Another Twitter-based study comes from Hanson and colleagues (2013a). They performed a qualitative analysis of the quantity and content of tweets containing the drug name ‘Adderall’. Hanson recorded 213,633 Adderall-related tweets over six months, with a peak coinciding during the examination period. These tweets were also analysed for content relating to motives, side effects, poly-use and possible normative influence. It was concluded that Adderall discussions through social media outlets such as Twitter, may contribute to normative behaviour regarding its abuse (Thanki et al., 2016: 117).
The limitations of discussing social media in relation to its portrayal of drug consumption comes from the fact that social media is a relatively new concept, and again vastly under-researched in terms of this topic. Therefore, data and theories and very limited and it is hard to draw comparison and correlations between social identity and social media. However, from the data found, social media clearly contrasts mass media, as it suggests that social media allows for less negative perceptions. This could be because people are able to portray a distorted view of their life in which they can make poly-drug use seem favourable, making viewers believe that it is normal behaviour.
“The transition from adolescence to young adulthood is a crucial period in which experimentation with illicit drugs, in many cases, begins. Drugs may have a strong appeal to young people who are beginning to struggle from independence as they search for their identity. Because of innate curiosity, thirst for new experience, peer pressures and resistance to authority, sometimes low self-esteem problems in establishing interpersonal relationships, young people are susceptible to the culture of drugs”, (UN Commission Document 1999, 14:4).
As the previous section highlighted, popular culture, in particular music, was a catalyst for recreational drug use to become culturally accommodated amongst a vast amount of conventional young people. Parker and colleagues argue that ‘it was the watershed whereby drugs moved from subculture status to become part of mainstream youth culture’, (Parker et al., 1995: 24). Drug users are now as likely to be female as male and come from all social and academic backgrounds; therefore, they could no longer be simply written off as ‘delinquent, street-corner, no-hopers’, (Parker et al., 1998: 1-2). Due to the magnitude of these changes, licit and illicit drug use could no longer be adequality explained by either subcultural theory or traditional notions of deviance – hence the creation of the normalisation thesis.
The term ‘normalisation’ is fundamentally concerned with how ‘a deviant, often subcultural population or their deviant behaviour can be accommodated into a larger grouping or society,’ (Parker et al., 1998: 152). The term can be used in various contexts; therefore, Parker and colleagues utilised the concept as a way of exploring and explaining the unprecedented increase of drug use of young adults throughout the 1990s. Parker and colleagues describe normalisation concerning recreational drug use as follows:
“Normalisation cannot be reduced to the intuitive phrase ‘it is normal for young people to take drugs’; that is both to oversimplify and overstate the case. We are concerned only with the spread of abnormal activity and associated attitudes from the margins to the centre of youth culture, where it joins many other accommodated ‘deviant’ activities such as excessive drinking, casual sexual encounters and daily cigarette smoking … Normalisation need not be concerned with absolutes; we are not even considering the possibility that most you Britons will become illicit drug users”, (Parker et al., 1998: 152 – 153).
Parker and colleagues (1998) acquired evidence for the normalisation thesis from the North West Longitudinal Study, which began in 1991 and tracked over 700 young people to assess how they developed attitudes and behaviours surrounding drugs. They found that 91.1% of respondents had been offered an illicit drug and that drugs were becoming more routinely available in locations such as schools, colleges, pubs and clubs. The study also revealed how six in ten respondents had tried an illicit drug and found precise closure to gender and social class differences. Most importantly, Parker’s study revealed how culturally accommodated drug use was becoming as a result of broader social changes, which has altered young people’s experiences of growing up in late modernity. This further suggests that 9% of participants that have not been offered drugs are ‘abnormal’.
The normalisation thesis is one of the most significant theoretical developments to have emerged in youth and drug studies literature; this is because it differed from previous criminological and psychological theories that associated drug use with deviance or resistance, (Pennay et al¸ 2016: 187).
Manning (2013) comments on the normalisation thesis, adding that there is a strong case for viewing drug consumption and its cultural practices as occupying a more visible position within contemporary popular cultures. Of course, this view is dependent on the normalisation thesis; the argument being that recreational drug use is now so familiar to those aged 35 and below that it should be regarded as ‘normal’, (Manning, 2013: 49). This is supported by Taylor (2008) who believes that in the context of the normalisation debate, drug use in the UK as well as the media’s reporting of drugs, drug consumption and drug-related crime has become such a regular force and indeed a normal image, (Taylor, 2008: 371).
Whilst normalisation does not necessarily mean that everyone partakes in drug consumption, it implies that non-acquaintance with drugs has become the deviation. MacDonald and Marsh (2002) usefully suggest that ‘differentiated normalisation’ may be occurring, with many adolescents abstaining from drug consumption, and some being frequent recreational users – a minority being dangerous, problematic drug addicts, (Carrabine, 2014: 273).
In terms of the media’s negative representation of drug use creating normalisation, Young (1971) highlights that stigmatisation from mass media may be used to enable or causes those who use drugs to affirm their identities as deviant and rebellious members of subcultures that differ from ‘straight’ society, (Carrabine et al., 2014: 272). In terms of popular culture, due to the vast amount of recording artists that partake in drug consumption and exude a drug style, it’s more than likely that to individual’s engaging with these musicians, drug consumption is normal behaviour as someone with immense amounts of popularity and fame is showing it to be an acceptable behaviour.
However, Shiner and Newburn (1997, 1999) argued that the normalisation thesis tends to exaggerate the degree of change that has taken place within contemporary society, and, that drug consumption remains a minority pursuit within youth culture.
Moving on, Tajfel and Turner (1979) proposed that the social identity theory emphasised obtained attitudes that mediate an individual’s identification with a specific social group (Hammersley et al., 2001: 137). This implies that an individual may act or respond differently depending on their diverse social groups. Stets and colleagues (2000) believe that social identity is a person’s knowledge that her or she, belongs to a specific social category or group; a social group is considered to be a set of individuals who hold a common social identification or view themselves as members of the same social category. Through a subconscious social comparison process, similar individuals are categorised and labelled ‘in-group’; individuals who differ are categorised as the ‘out-group’, (Stets et al., 2000: 225). Miller (2014) agrees with this, extending to say that many individuals, particularly adolescents and young adults, are willing to experiment with drugs simply because their peer group are favourably inclined to do the same. Thus, if an individual perceives a favourable response from peers for drug experimentation, they are more likely to engage in this behaviour, (Miller et al¸ 2014: 318).
Hammersley and colleagues (2001) exemplify cannabis in relation to social identity; they question that very little is known about contemporary experiences surrounding cannabis use and the problems that mass users encounter and how it fits into their everyday lives. Hammersly notes that cannabis use (or any substance use) can only relate to identity in one of two ways; the first being that cannabis is used to signify membership to a group or cannabis does not signify membership to a group, (Hammersley et al, 2001: 137). They note that as well as being a signifier for identity, it could also signify social setting as there is unlikely to be homogenous social group of cannabis use.
The core research question that was being tested was ‘how drug use is presented within popular culture and media can have an effect on an individual’s identity’ which is something this literature-based discussion has achieved. Both popular culture and media outlets are seen to create and support the normalisation thesis through different sources, as well as impacting on a person’s social identity in differing ways.
Beginning with popular culture, musicians are showing drug consumption in a positive light through their fame and popularity, and, even though they may not have the intention of putting this trait onto their fans, this trend is being replicated. This is affecting an individual’s social identity as people are beginning to identity with the social group surrounding a particular band and, subconsciously or not, cultivating their behavioural patterns and style. In terms of the normalisation thesis, as individuals continually engage with this drug behaviour, it becomes a prominent normal image for them to encounter.
However, television and cinema are seen to have the opposite effect as they tend to show more realistic images of drug consumption such as addiction and squalid living conditions. Although the audiences may realise that this is dramatized, it may have a direct impact on what social groups they identify with.
In terms of mass media, newspaper and region-specific broadcasts clearly have a direct impact on both the normalisation thesis and social identity theory through their use of moral panics. Moral panics serve to distort information to create fear within society; although this presented imagery can be considered false, the repeated reporting of drug scares serves to highlight that drug consumption and experimentation is a ‘normal’ part of society even though it threatens societies moral laxity. This could also affect a member of society’s social identity as an individual may become apprehensive to affiliate themselves with a social group known for drug experimentation or known to accommodate those who partake in drug consumption.
Social media endeavours to offer a different perception to drug use, suggesting that there is a large number of individuals who socially accept those who take drugs and that this ‘war on drugs’ rhetoric is nothing more than a media scare tactic. This may be due to the fact that social media allows its users to create its own media and realities; for example, those who find drug consumption socially acceptable are able to block out negative media stories that stem from drugs and only receive positive interpretations.
Both popular culture and media highlight that, whether presenting drug use positively or negatively, these trends are perennial. As Lewis (1980) states, there has been a long-standing linkage between new forms of popular music and immoral behaviour, such as drug use, (Lewis, 1980: 176). For example, the 1950s and 60s saw a link between Rock and Roll and alcohol and the 1960s and 70s with protest rock, marijuana and LSD. This continued with the 1980s and 1990s with genres such as Indie and Brit-pop and drugs such as ecstasy and MDMA.
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The core research question to be tested for this dissertation is 'how drug use is presented within popular culture and media, and how this can affect an individual's identity'.
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The core research question to be tested for this dissertation is 'how drug use is presented within popular culture and media, and how this can affect an individual's identity'. One of the aims of this dissertation is to conclude whether listening to specific genres of music, corresponds to drug consumption or drug experimentation.