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Pilot Trial of Contingency Management for Long-Term Cannabis Abstinence

Not Applicable
Completed
Conditions
Cannabis Use
Adolescent Behavior
Interventions
Behavioral: Contingency Management
Registration Number
NCT03786224
Lead Sponsor
Massachusetts General Hospital
Brief Summary

This study is a critically important first-of-its-kind investigation of the potential research utility of using contingency management to examine long-term changes in cannabis use with six months of abstinence. These pilot data will inform a later trial which will focus on testing the longitudinal relationships between adolescent cognition and cannabis use, questions of high and growing public health significance given adolescents' increased access to cannabis with legalization.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
6
Inclusion Criteria
  • Male and female adolescents actively enrolled in a middle or high school in the Boston area who are between the ages of 13 and 19 (inclusive);
  • Average use of cannabis at least 3 times per week during the 3 months prior to study enrollment;
  • Cannabis use reported within 7 days of study enrollment;
  • No immediate plan to discontinue cannabis use;
  • Have a parent or legal guardian who is competent and willing to provide written informed consent for the active study phase (if under the age of 18);
  • Competent and willing to provide written informed assent for the active study phase (if under the age of 18);
  • Competent and willing to provide written informed consent (if age 18 or older);
  • Able to communicate in English language;
  • Have a parent/guardian who can communicate in English language;
  • Able to commit to 27 study visits in approximately 6 months;
  • Able to safely participate in the protocol and appropriate for outpatient level of care, in the opinion of the investigator.
Exclusion Criteria
  • Any severe developmental delays (including, but not limited to, Autism Spectrum Disorder, Intellectual Disability, and Down Syndrome).

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
AbstinentContingency Management-
Primary Outcome Measures
NameTimeMethod
Continuous Abstinence Via Progressive Declines in Urine THCCOOHSix months

Cannabis abstinence will be indexed by progressively decreasing quantitative levels (ng/mL) of 11-nor-delta-9-THC-9-carboxylic acid (THCCOOH), the primary cannabis metabolite, in urine. Residual cannabinoid excretion will be differentiated from new cannabis exposure using a statistical model developed by Schwilke and colleagues (2011). This model was empirically derived from urine CN-THCCOOH concentration ratios of consecutively collected specimen pairs (current specimen/prior specimen). This model takes into account the time between collection of specimens, which enhances the accuracy of prediction of new cannabis use. This formula yields an expected CN-THCCOOH ratio associated with specimen pairs during abstinence, and observed ratios that exceed this expected value are interpreted as new cannabis use.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Massachusetts General Hospital

🇺🇸

Boston, Massachusetts, United States

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