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N/A N=59 Randomized Treatment

Behavioral Treatment of Adolescent Substance Use

Substance Use Disorders

Enrolled (actual)
59
Serious AEs
0.0%
Results posted
May 2021
Primary outcome: Primary: Any Cannabis Abstinence — 13; 18 participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Intensive Outpatient Treatment (IOP) + Contingency Management (CM) (Behavioral); Working Memory Training (Behavioral)
Age
Pediatric, Adult · 12+ yrs
Sex
All
Sponsor
Dartmouth-Hitchcock Medical Center
Primary completion
Feb 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Any Cannabis Abstinence
13; 18
PRIMARY
Weeks of Continuous Cannabis Abstinence
7.15; 4.88
SECONDARY
Any Days of Cannabis Use
11; 14
SECONDARY
Days of Cannabis Use
32.5; 24.5
SECONDARY
Any Cannabis Abstinence Across Four Treatment Strategies
12; 12; 14; 11
SECONDARY
Weeks of Cannabis Abstinence Across Four Treatment Strategies
6.17; 7.42; 5.29; 7.82

Summary

This study will continue research designed to improve treatment outcomes for adolescent substance use disorders by integrating neuroscience- and behaviorally-based treatments. In particular, this project will be the first to evaluate whether Working Memory Training can enhance cognitive function and reduce impulsive decision making to improve abstinence outcomes. In addition, an adaptive abstinence-based incentive program will be evaluated as a new method for intervening with those who do not respond to their first-line treatment.

Eligibility Criteria

Inclusion Criteria

Participants must be 12 to 26 years of age, must live at home with the parent who will participate, report using marijuana during the previous 30 days or provide a marijuana-positive urine test, meet criteria for cannabis abuse or dependence, and have a parent who can participate.

Exclusion Criteria: DSM criteria for dependence (likely to be adjusted for DSM-5 Use Disorder) on alcohol or other drugs other than marijuana (use of or meeting criteria for abuse of other substances will not be an exclusion criterion), active psychosis, severe medical or psychiatric illness limiting participation, or pregnant or breast-feeding.

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02063984). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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