Brief Family-Based Cannabis Use Intervention for Youth With Early Juvenile Justice Involvement
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Brief Family Based Intervention, Parenting Psychoeducation.
- Who it may be relevant to
- Registry conditions: Cannabis Use, Delinquency. Basic parameters: 12 years — 16 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The goal of this randomized clinical trial is to learn if a brief family-based intervention in effective in reducing cannabis use and delinquency in youth participating in juvenile diversion. The main questions it aims to answer are: Hypothesis 1: the intervention will be (a) feasible, as evidenced by enrollment rates (\> 80%), follow-up rates (\> 80%), and withdrawal rates (\< 20%); and (b) acceptable, as evidenced by \> 80% of treatment evaluation ratings in the highest two Likert rating categories and positive exit interview feedback. Hypothesis 2: those parents in the experimental condition, as compared to the active comparison psychoeducation condition, will evidence greater improvement over time in the hypothesized family-level mechanisms proposed in the intervention (i.e., parenting practices and parent well-being) as well as in youth-level outcomes, including cannabis use, recidivism, and HIV/STI risk. Researchers will compare the family-based treatment to parenting psychoeducation. Caregiver and youth participants will complete measures relevant to primary outcomes and putative mechanisms at baseline, 3-month, and 6-month follow-ups.
Detailed description
Approximately 50% of youth with early juvenile justice system (JJS) involvement (i.e., diverted youth with less severe or first-time arrest histories) screen positive for cannabis use.Cannabis use is especially problematic for youth with early JJS involvement, given research suggesting that cannabis use is linked with continued and chronic involvement in the JJS. Moreover, cannabis use among justice-involved youth (JIY) is also associated with other consequences, including HIV/STI risk behaviors (e.g., lack of condom usage). Early JIY who use cannabis also differ from youth without justice involvement, such that they are more likely to belong to marginalized communities and also evidence worse family functioning. Thus, this population warrants specialized interventions targeting cannabis use and associated consequences.
To date, the most effective cannabis and other substance use interventions for youth in the JJS are largely intensive, personalizable family-based models (e.g., multisystemic therapy), which also have documented efficacy in reducing the risk for HIV/STIs and long-term criminal involvement. However, these models were intended for youth with serious juvenile justice involvement and, thus, early JIY are rarely referred to these services.21 Such models are also likely overly intensive for treating cannabis use among early JIY. Despite evidence suggesting parenting practices, parent well-being, and family functioning are linked to cannabis use, delinquency, and HIV/STI risk behaviors for early JIY, there is a concerning lack of family-based services addressing cannabis use and other risk behaviors specifically developed for early JIY. Therefore, there is still a need for family-based interventions for early JIY. However, these interventions should be briefer in nature, so that they can be implemented as part of a larger continuum of care within the JJS.
The primary goal of this NIDA-funded K23 research project is to adapt an existing evidence-based family-based intervention to families of early JIY who screen positive for cannabis use. The proposed 6-session, modular, family-based intervention will be delivered via telehealth and primarily focus on changing parent behaviors, consistent with prior family-based interventions for the present population.The modules will focus on: 1) psychoeducation delivered in motivational interviewing style (e.g., encouraging caregivers' role in preventing substance use), 2) parenting practices (e.g., supervision, managing peer relations), and 3) parent well-being (e.g., increasing social support). Family intervention strategies across these modules will be adapted from existing evidence-based interventions and personalized to best meets each youth and parents' clinical needs (consistent with NIDA Goal 2.3). Our objective will be to understand the initial efficacy of the intervention in treating adolescent cannabis use and other important, related outcomes (e.g., HIV/STI risk behaviors) through a pilot randomized clinical trial (RCT).
Primary aim. Evaluate the acceptability, feasibility, and initial family-level mechanisms and youth substance-use related outcomes of a brief, family-based intervention for early justice-involved youths. A pilot RCT (N = 60) will be conducted in which youth and families will be randomized to either the proposed family-based intervention or parent psychoeducation. The youth and their primary caregiver will participate in these conditions via telehealth and will complete follow-up assessments at 3 and 6 months. H1: the intervention will be (a) feasible, as evidenced by enrollment rates (\> 80%), follow-up rates (\> 80%), and withdrawal rates (\< 20%); and (b) acceptable, as evidenced by \> 80% of treatment evaluation ratings in the highest two Likert rating categories and positive exit interview feedback. H2: is that those parents in the experimental condition, as compared to the active comparison psychoeducation condition, will evidence greater improvement over time in the hypothesized family-level mechanisms proposed in the intervention (i.e., parenting practices and parent well-being) as well as in youth-level outcomes, including cannabis use, recidivism, and HIV/STI risk.
Interventions
- Behavioral Brief Family Based Intervention
The intervention is proposed as 6 sessions long and will have the following modules: 1) Introduction to Treatment; 2) Parent Training Strategies (clinician must cover at least 1 topic from this module); 3) Improving Parent Well-Being (clinician must cover at least 1 topic from this module); and 4) Treatment Termination and Future Planning. Youth may attend the first and last session, in addition to other relevant sessions (e.g., household rules/consequences); parents will attend every session. C - Behavioral Parenting Psychoeducation
Psychoeducation in the comparison group will involve 6 hour-long sessions delivered via secure videoconferencing focused on providing parents with key developmental knowledge regarding adolescence and parenting. To differentiate the psychoeducation provided in the intervention group, sessions will focus on typical adolescent development and parenting knowledge derived from Centers for Disease Control publicly available information.The first two sessions will provide information about typical dev
Primary outcome measures
- Timeline Follow-Back [Time frame: The Timeline Follow-Back will be administered at baseline, 3-months, and 6-months post baseline.]
- Official arrest records [Time frame: Official arrest records will be collected for the 12 months following baseline.]
- Marijuana Adolescent Problem Inventory [Time frame: We will collect this measure at baseline, 3-months, and 6-months post baseline.]
Eligibility criteria
Inclusion Criteria: 1) parent and youth are English or Spanish speaking, 2) legal guardian is able to consent for their own and juvenile's participation, 3) youth flags for CU on either the Drug/Alcohol scale of the MAYSI-2 or on the CRAFFT 2.0, 4) not currently in substance use treatment elsewhere, and 5) youth currently residing in the community.
Exclusion Criteria: Youth and parents will not be able to participate in the present study if they have developmental or cognitive delays or a major psychiatric disorder, documented in the intake materials, that would interfere with completing consent, assessments, or the intervention
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Single group
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
United States · 1 center
- Bradley-Hasbro Children's Research Center — Providence
Identifiers
NCT: NCT07700849 · 2079613 · K23DA058014