Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07218471

Cannabis Reduction and Functional Outcomes

Led by Medical University of South Carolina · Updated on 2026-03-19

176

Participants Needed

1

Research Sites

202 weeks

Total Duration

On this page

Sponsors

M

Medical University of South Carolina

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study evaluates the effects of cannabis use reduction among adults diagnosed with cannabis use disorder (CUD). Participants will undergo an 8-week intervention combining motivational interviewing, computerized cognitive behavioral therapy (CBT4CBT), and financial incentives for reduction in urinary cannabinoids. The study aims to assess improvements in cannabis-related problems, sleep, cognitive performance, CUD severity, and quality of life.

CONDITIONS

Official Title

Cannabis Reduction and Functional Outcomes

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18+
  • Urinary cannabinoid level 65 50 ng/mL
  • Diagnosis of cannabis use disorder (mild, moderate, or severe) according to DSM-5
  • Willingness to attempt cannabis reduction
  • Completion of Intake Visit
Not Eligible

You will not qualify if you...

  • Serious medical or psychiatric conditions
  • Pregnancy or breastfeeding
  • Cannabis use in past 30 days was for medical purposes only
  • Cannabis use reduction may worsen a pre-existing condition
  • Cognitive or understanding difficulties preventing informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical University of South Carolina

Charleston, South Carolina, United States, 29425

Actively Recruiting

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Research Team

R

Rachel Tomko, PhD

CONTACT

E

Erin McClure, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

0

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