Cannabis Use Disorder Clinical Trial
— RECABOfficial title:
The Cost-effectiveness of Contingency Management Compared to Standard Cognitive Behavioral Treatment for Treating Cannabis Use Disorder in Youth: A Randomized Controlled Trial
The goal of this clinical trial is to investigate the (cost-)effectiveness of contingency management (CM) compared with Cognitive Behavioural Therapy (CBT) for the treatment of cannabis use disorder (CUD) in youth (16-22 years). The main questions it aims to answer are: - What is the efficacy of 12 weeks outpatient CM versus CBT in youths with a CUD, in terms of cannabis abstinence during the intervention period? - What is the long-term efficacy of CM versus CBT at 6- and 12-months follow-up (FU)? - What is the cost-effectiveness of CM versus CBT at 12-months FU from a societal perspective? Study hypotheses are: 1. CM will result in more cannabis-abstinent days than CBT during the intervention; 2. CM is more effective and cost-effective than CBT at 12 months follow-up. Eligible patients (n=154) will be randomly assigned to either 12 weeks of outpatient CM or CBT. Assessments are conducted by trained research-assistants at baseline, after 6, 12, 26 and 52 weeks, and twice-weekly during treatment and consist of questionnaires, a computer task and collection of urine samples. Primary endpoint is the number of biochemically verified cannabis abstinent days in the 12-week treatment period. Key secondary endpoint: Treatment response: 50% or more reduction in cannabis use days in the past 4 weeks, compared with baseline. The primary outcome will be modelled in the intention-to-treat population in a (negative binomial) regression analysis with treatment group as independent variable and stratification variables as covariates. Cost-effectiveness and cost-utility analysis (CEA; CUA) will be performed from a societal perspective. CEA: Treatment response is the central clinical endpoint for calculations of incremental costs per responder. CUA: Incremental costs per QALY (based on EuroQoL).
Status | Recruiting |
Enrollment | 154 |
Est. completion date | January 2027 |
Est. primary completion date | March 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 16 Years to 22 Years |
Eligibility | Inclusion Criteria: - Youths (16-22 years) seeking treatment for a primary CUD - Regular cannabis use (=14 days) in past 4 weeks - Intention to cease cannabis use during intervention - Able and willing to attend the treatment center and submit urine samples under supervision twice-weekly - Informed consent. Exclusion Criteria: - Health contra-indications (e.g., acute psychosis/suicidality) - Insufficient Dutch language. |
Country | Name | City | State |
---|---|---|---|
Netherlands | Antes Youz | Rotterdam | |
Netherlands | Brijder | the Hague | |
Netherlands | Novadic-Kentron | Vught |
Lead Sponsor | Collaborator |
---|---|
Parnassia Addiction Research Centre | Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), Amsterdam University of Applied Sciences, Antes, Brijder Verslavingszorg, Het Zwarte Gat, Leiden University Medical Center, Novadic-Kentron, Trimbos |
Netherlands,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cannabis-abstinent days (biochemically verified) | Number of biochemically verified cannabis-abstinent days during the 12-week intervention period | 12 weeks | |
Secondary | long-term 'treatment response' | defined as 50% or more reduction in cannabis use days in the 4 weeks preceding week 12 (end-of-treatment), and week 26 and 52, compared with baseline. | 52 weeks | |
Secondary | Incremental costs per treatment responder | Incremental cost-effectiveness ratio (ICER) per treatment responder (see above) will be determined based on the incremental costs and effects of CM compared with CBT. | 52 weeks | |
Secondary | Incremental costs per QALY | Incremental costs per quality-adjusted life years (QALY) gains based on the The 5-level EQ-5D version (EQ-5D-5L) | 52 weeks |
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