ClinicalTrials.Veeva

Menu

A Brief Intervention for Cannabis Use (Bloom)

Medical University of South Carolina (MUSC) logo

Medical University of South Carolina (MUSC)

Status

Enrolling

Conditions

Cannabis Use Disorder

Treatments

Behavioral: Health Education (HealthEdu)
Behavioral: Bloom

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06395389
K23DA058077 (U.S. NIH Grant/Contract)
Pro00133931

Details and patient eligibility

About

The purpose of this study is to compare two brief interventions targeting potentially problematic cannabis use in emerging adults (ages 18-25). Brief interventions are two 40-50 minute sessions separated by 1 week. Eligible emerging adults will complete a detailed cannabis assessment (biological and self-report), followed by one of the two brief interventions, and three follow-up assessments: one immediately after the second session and at 1- and 3-months post-intervention. Assignment to the brief intervention is random. Salivary samples will be collected at baseline, post-intervention, and both follow-ups, for a total of 4 samples, to be tested for tetrahydrocannabinol (THC) and cannabidiol (CBD).

Full description

Cannabis is the most widely used federally illicit substance among emerging adults (age 18-25) in the U.S., and frequent cannabis use is associated with myriad long-term health, social, and academic/occupational consequences. Despite this, rates of perceived risk of daily/regular cannabis use have steadily declined over the past two decades, and this is associated with increased frequency of use, a risk for for Cannabis Use Disorder (CUD). Brief interventions (BIs) are among the most frequently used approaches for addressing problematic or potentially problematic substance use in non-treatment-seeking adolescents and young adults. Although several cannabis brief interventions have been developed and tested to date, meta-analyses indicate that the efficacy of these interventions for emerging adults is mixed and the quality of studies is low, suggesting that novel approaches and rigorous methodology are necessary to improve efficacy. The current study will evaluate the feasibility, acceptability, and preliminary efficacy of a novel cannabis BI for emerging adults who frequently use cannabis.

Enrollment

62 estimated patients

Sex

All

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Ages 18-25
  • Self-Report report cannabis use on at least 20 days of the past 30 days.
  • Completion of an Intake Visit (PRO #94743)
  • Submit a positive urine cannabinoid test during the Intake Visit

Exclusion criteria

  • Currently engaged in substance use treatment for any type of substance use or currently treatment seeking
  • History of substance use treatment for any type of substance
  • Severe alcohol use disorder or presence of any substance use disorder (SUD) requiring a higher level of care
  • Significant or acutely unstable medical or psychiatric problems (i.e., psychosis, mania) that would contraindicate research procedures, interfere with safety, compromise data integrity, or preclude consistent study participation
  • Significant risk of suicide or homicide

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

62 participants in 2 patient groups

Health Education (HealthEdu)
Active Comparator group
Description:
Brief intervention providing recommendations/advice for good sleep hygiene, nutrition and physical activity, stress, and relationships.
Treatment:
Behavioral: Health Education (HealthEdu)
Bloom
Experimental group
Description:
Brief intervention providing personalized discussion of values/goals, reasons for cannabis use, and strategies to help live in line with values and achieve goals.
Treatment:
Behavioral: Bloom

Trial contacts and locations

1

Loading...

Central trial contact

Kathryn Gex, Ph.D.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems