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Rewards for Cannabis Abstinence-study (RECAB)

Primary Purpose

Cannabis Use Disorder

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Abstinence-focused Contingency Management (CM) - stand alone
Standard Outpatient Cognitive Behavioural Therapy (CBT)
Sponsored by
Parnassia Addiction Research Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cannabis Use Disorder focused on measuring contingency management, cognitive behavioural therapy, CM, CBT, cost-effectiveness, youth, randomized controlled trial (RCT)

Eligibility Criteria

16 Years - 22 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Abstinence-focused Contingency Management (CM)

    Cognitive Behavioural Therapy (CBT)

    Arm Description

    Youths receive 12 weeks of outpatient abstinence-focused CM consisting of providing incentives for cannabis abstinence, based on twice-weekly rapid test urinalysis.

    Youths receive 12 weeks of outpatient usual care CBT consisting of once-weekly 60-minute sessions according to the standard CBT youth protocol by a trained psychologist.

    Outcomes

    Primary Outcome Measures

    Cannabis-abstinent days (biochemically verified)
    Number of biochemically verified cannabis-abstinent days during the 12-week intervention period

    Secondary Outcome Measures

    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.
    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.
    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)

    Full Information

    First Posted
    April 18, 2023
    Last Updated
    April 18, 2023
    Sponsor
    Parnassia Addiction Research Centre
    Collaborators
    Leiden University Medical Center, Brijder Verslavingszorg, Antes, Novadic-Kentron, Amsterdam University of Applied Sciences, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), Trimbos, Het Zwarte Gat
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05836207
    Brief Title
    Rewards for Cannabis Abstinence-study
    Acronym
    RECAB
    Official Title
    The Cost-effectiveness of Contingency Management Compared to Standard Cognitive Behavioral Treatment for Treating Cannabis Use Disorder in Youth: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 2023 (Anticipated)
    Primary Completion Date
    January 2026 (Anticipated)
    Study Completion Date
    August 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Parnassia Addiction Research Centre
    Collaborators
    Leiden University Medical Center, Brijder Verslavingszorg, Antes, Novadic-Kentron, Amsterdam University of Applied Sciences, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA), Trimbos, Het Zwarte Gat

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    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).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cannabis Use Disorder
    Keywords
    contingency management, cognitive behavioural therapy, CM, CBT, cost-effectiveness, youth, randomized controlled trial (RCT)

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    154 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Abstinence-focused Contingency Management (CM)
    Arm Type
    Experimental
    Arm Description
    Youths receive 12 weeks of outpatient abstinence-focused CM consisting of providing incentives for cannabis abstinence, based on twice-weekly rapid test urinalysis.
    Arm Title
    Cognitive Behavioural Therapy (CBT)
    Arm Type
    Active Comparator
    Arm Description
    Youths receive 12 weeks of outpatient usual care CBT consisting of once-weekly 60-minute sessions according to the standard CBT youth protocol by a trained psychologist.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Abstinence-focused Contingency Management (CM) - stand alone
    Intervention Description
    Outpatient abstinence-focused contingency management (CM) as stand-alone treatment (12 weeks). Monetary incentives (vouchers) are provided for cannabis abstinence, based on twice-weekly rapid test urinalysis and an escalating reward scheme with bonuses. Urine samples are collected at the treatment centre during 15-minute sessions by a trained CM-practitioner. For each cannabis-negative urine, patients receive a monetary voucher starting at €5 and escalating to max. €35 after eight consecutive weeks of cannabis abstinence, with an additional €10 bonus after two consecutive cannabis-negative urines. The voucher-value is reset to €5 after a cannabis-positive urine test. Total earnings can be max. €675 for 12 weeks of consecutive cannabis abstinence (average: €8 p/day). Youths sign an agreement stating that vouchers must be spent on recovery-oriented goals.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Standard Outpatient Cognitive Behavioural Therapy (CBT)
    Intervention Description
    CBT is the usual care first line treatment for CUD in youth, in the Netherlands. CBT for CUD is focused on learning cognitive, emotional, motivational and behavioral skills to reduce or cease cannabis use, and generally consists of 12 once-weekly 60-minute sessions and 'homework' exercise assignments, provided by a psychologist. Youths receive 12 weeks of outpatient usual care CBT consisting of once-weekly 60-minute sessions according to the standard CBT youth protocol by a trained psychologist. CBT-youths receive the same cannabis urine-testing procedures as CM-youths, but test results will not be disclosed to treatment staff or patient, and no rewards will be given for cannabis abstinence.
    Primary Outcome Measure Information:
    Title
    Cannabis-abstinent days (biochemically verified)
    Description
    Number of biochemically verified cannabis-abstinent days during the 12-week intervention period
    Time Frame
    12 weeks
    Secondary Outcome Measure Information:
    Title
    long-term 'treatment response'
    Description
    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.
    Time Frame
    52 weeks
    Title
    Incremental costs per treatment responder
    Description
    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.
    Time Frame
    52 weeks
    Title
    Incremental costs per QALY
    Description
    Incremental costs per quality-adjusted life years (QALY) gains based on the The 5-level EQ-5D version (EQ-5D-5L)
    Time Frame
    52 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    16 Years
    Maximum Age & Unit of Time
    22 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    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.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Eva Garssen, MsC
    Phone
    +3188 358 20 34
    Email
    e.garssen@brijder.nl
    First Name & Middle Initial & Last Name or Official Title & Degree
    Renske Spijkerman, PhD
    Phone
    +31630661532
    Email
    renske.spijkerman@brijder.nl
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Renske Spijkerman, PhD
    Organizational Affiliation
    PARC
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Vincent Hendriks, Prof. dr.
    Organizational Affiliation
    PARC
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    First draft of datamanagement plan has been submitted to funding organisation.
    IPD Sharing Time Frame
    december 2028, 15 years

    Learn more about this trial

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