Intervention for Teens With ADHD and Substance Use

Sponsor
Florida International University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02502799
Collaborator
(none)
158
1
3
85
1.9

Study Details

Study Description

Brief Summary

Individuals with ADHD are at markedly high risk for increased substance use and Substance Use Disorder (SUD). Given the strong evidence for the negative trajectory of individuals with co-occurring ADHD and substance use initiation, the goal of this study is to conduct a controlled examination of a brief, early intervention (BEI) for substance modified for adolescents with ADHD. Importantly, this intervention will address individuals who are at risk for problems with substance use, but do not yet meet criteria for severe SUD.

Although brief interventions have been found to be effective in other populations, their efficacy in an ADHD population with emerging risk for substance use problems remains uninvestigated. This study aims to understand why some adolescents with ADHD and elevated risk for SUD respond to (BEI) and others do not. The investigators will test whether situational and individual characteristics predict substance use development and response to treatment. Further, this study will assess which types of additional treatment are most effective for youth who do not respond to the initial BEI. It is hypothesized that rates of adolescent substance use will be lower among adolescents who participate in study treatments.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Brief Early Intervention
  • Behavioral: Parent Training with Adolescent Cognitive Behavioral Therapy
  • Drug: Methylphenidate
Phase 3

Detailed Description

The goal of this study is to evaluate the efficacy of a brief early intervention (BEI) for reducing early alcohol and marijuana use in a group of 300 adolescents (age 12-16) with ADHD. All adolescents will receive the BEI based on the Teen Intervene program with the addition of enhanced decision making skills. Due to the existing support for the intervention and concern for randomizing families with adolescents at risk for worsening substance use outcomes into a control (no treatment) condition for one to two years, no control condition is used in the current design at the first level of intervention. Similarly, due to the time required to see a potential effect of the treatment (6 months post-brief intervention), a wait-list control condition was not considered.

Adolescents will be evaluated for treatment non-response at 6, 9, 12, 15, and 18 months post-treatment. Non-response is defined as non-normative use of alcohol, marijuana, or other drugs during the past 90 days. Tobacco products are excluded from consideration. Adolescents who demonstrate non-response to the initial BEI at any of the follow-up assessments will be randomized to one of the following conditions: 1) Continued monitoring of substance use with no additional treatment 2) Parent training and adolescent cognitive behavioral therapy (PT/ACBT) 3) PT/ACBT plus concurrent stimulant medication (PT/ACBT + MED). Participants who are randomized will be assessed at 6 months post-treatment and again one year later. The difference in days of substance use at the follow-up assessments among the three conditions will inform which type of intervention is best for youth who do not respond to the initial BEI.

Study Design

Study Type:
Interventional
Actual Enrollment :
158 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Intervention for Teens With ADHD and Substance Use
Study Start Date :
Jul 1, 2015
Anticipated Primary Completion Date :
Aug 1, 2022
Anticipated Study Completion Date :
Aug 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Continued Monitoring and Assessment

All participants will receive 5 sessions of BEI. Non-responders will then be randomized to one of three conditions. Participants randomized to the continued monitoring and assessment arm will receive no additional intervention. Primary and secondary outcomes will be monitored.

Behavioral: Brief Early Intervention
Adolescents receive 5 individual sessions designed to strengthen the following skills: problem-solving, resisting peer pressure, and coping with emotions. Parents join portions of 3 sessions.
Other Names:
  • BEI, Teen Intervene
  • Active Comparator: PT with ACBT

    All participants will receive 5 sessions of BEI. Non-responders will then be randomized to one of three conditions. For participants randomized to the PT with ACBT arm, parents will participate in behavioral parent training (PT) and adolescents will participate in cognitive behavioral therapy to reduce substance use (CBT).

    Behavioral: Brief Early Intervention
    Adolescents receive 5 individual sessions designed to strengthen the following skills: problem-solving, resisting peer pressure, and coping with emotions. Parents join portions of 3 sessions.
    Other Names:
  • BEI, Teen Intervene
  • Behavioral: Parent Training with Adolescent Cognitive Behavioral Therapy
    Participants receive 12 family sessions with individual adolescent, parent, and joint adolescent and parent time. Includes additional parent training in behavioral modification, adolescent and parent contracting, and adolescent decision-making skills.

    Active Comparator: PT with ACBT and Methylphenidate

    All participants will receive 5 sessions of BEI. Non-responders will then be randomized to one of three conditions. For participants randomized to the PT with ACBT and Methylphenidate arm, parents will participate in behavioral parent training (PT) and adolescents will participate in cognitive behavioral therapy to reduce substance use (ACBT). Adolescents will also receive methylphenidate.

    Behavioral: Brief Early Intervention
    Adolescents receive 5 individual sessions designed to strengthen the following skills: problem-solving, resisting peer pressure, and coping with emotions. Parents join portions of 3 sessions.
    Other Names:
  • BEI, Teen Intervene
  • Behavioral: Parent Training with Adolescent Cognitive Behavioral Therapy
    Participants receive 12 family sessions with individual adolescent, parent, and joint adolescent and parent time. Includes additional parent training in behavioral modification, adolescent and parent contracting, and adolescent decision-making skills.

    Drug: Methylphenidate
    Adolescents will receive methylphenidate.
    Other Names:
  • Concerta
  • Outcome Measures

    Primary Outcome Measures

    1. Past 90-day substance use [Assessed at 6 months after randomization to treatment]

      Number of days during which substances were used in the past 90 days

    2. Evidence of illicit substances in urine screen [Assessed at 6 months after randomization to treatment]

      Urine analysis indicates presence of illicit substance(s)

    Secondary Outcome Measures

    1. Parent-adolescent conflict [Assessed at 6 months after randomization to treatment]

      Parent and youth report of conflict on the Conflict Behavior Questionnaire

    2. Disruptive Behaviors [Assessed at 6 months after randomization to treatment]

      Adolescent disruptive behaviors as measured by adolescent self-report and parent report on the Deviant Behavior Scale and the Disruptive Behavior Questionnaire.

    3. Likelihood of future substance use [Assessed at 6 months after randomization to treatment]

      Youth self-report of likelihood of future substance use during the next 3 months and the next year

    4. Youth impairment [Assessed at 6 months after randomization to treatment]

      Level of impairment experienced across multiple domains of functioning (e.g., at school, at home, with peers) as measured by parent report and adolescent self-report on the Impairment Rating Scale.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years to 16 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Diagnosis of ADHD

    • At elevated risk for substance use problems as evidenced by at least one general risk factor (e.g., elevated symptoms of ODD or CD, elevated conflict with parents, low parental monitoring, or academic failure) and at least one substance use specific risk factor (e.g., non-normative use of alcohol or other drugs, use of cigarettes or e-cigarettes, parental substance use problems, family history of substance use problems, peer or sibling substance use).

    Exclusion Criteria:
    • IQ < 80

    • Current substance use disorder meeting DSM-IV criteria for the severe qualifier

    • Psychotropic medications for ADHD or any other condition

    • Active medical conditions that could be worsened by stimulants unless approved for participation by the treating physician

    • Diagnosis of bipolar disorder, schizophrenia, and/or other psychotic disorder

    • Diagnosis of autism spectrum disorder (ASD) with a severity level of 2 or 3 or significant intellectual or language impairment

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Florida International University Center for Children and Families Miami Florida United States 33199

    Sponsors and Collaborators

    • Florida International University

    Investigators

    • Principal Investigator: William E Pelham, PHD, Florida International University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Florida International University
    ClinicalTrials.gov Identifier:
    NCT02502799
    Other Study ID Numbers:
    • DA034731
    First Posted:
    Jul 20, 2015
    Last Update Posted:
    Oct 4, 2021
    Last Verified:
    Sep 1, 2021

    Study Results

    No Results Posted as of Oct 4, 2021