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Active, not recruitingNCT07011615Updated Jun 3, 2026

Feasibility/Acceptability of a Brief Motivational Intervention for Frequent/High-Intensity Cannabis Use

An interventional study of Brief Motivational Mobile Health (mHealth) Intervention and Psychoeducational Attention Control (AC) in Cannabis Use, sponsored by University of Washington. Active, not recruiting at 1 site in United States. Open to participants aged 18 Years to 29 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-03.

Sponsored by University of Washington · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 29 Years
Sex
All
01

Study summary

The study aims to develop a novel brief motivational mobile health (mHealth) intervention for frequent and/or high-intensity cannabis use for non-collegiate young adults. A total of 120 young adults (ages 18-29, not enrolled at or attending a 4-year college or university) will be randomized to receive a mHealth intervention with text messages for five weeks or to an online resource/program with psychoeducation information about cannabis. The mHealth intervention will focus on prompting the young adult to reflect on their journey with cannabis and to reflect on their personal goals and how cannabis is reflected in these goals. Additional mini-modules are included related to topics such as motivations for use, perceived norms and tracking cannabis use. Participants will return to the program each week to reflect on the prior week and reflect on goals for the upcoming week. All participants will complete a program satisfaction survey and complete follow-up assessments at 3- and 6-months post-program.

02

Conditions studied

  • Cannabis Use
03

In context

Lead sponsor

University of Washington is the lead sponsor of 1,397 studies on the registry; 225 are open to participants now.

Of its 154 completed or terminated interventional studies of FDA-regulated products, 132 (86%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 29 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 18-29 years old
  • reside in Washington or Oregon State
  • have valid email address
  • report using cannabis on 15 or more days in the past month, and/or using high THC concentration products in the past month (>60% THC)
  • have a mobile phone and agree to receive text messages and has an internet browser
  • not attending or enrolled at a 4-year college or university or graduate/professional school.

Exclusion criteria

Exclusion Criteria:

  • females who are pregnant or trying to become pregnant
  • those who are in substance abuse treatment at screening
  • those attending or enrolled at a 4-year college or university or graduate/professional school.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Brief Motivational Mobile Health (mHealth) Intervention

    Participants randomized to the Brief Motivational mHealth intervention will experience a five week self-directed web-based intervention with text messages.

    Behavioral: Brief Motivational Mobile Health (mHealth) Intervention

  • Other
    Psychoeducational Attention Control

    Participants randomized to the control group will receive a program to learn more about psychoeducational information about cannabis. They will receive psychoeducational material via text messages.

    Other: Psychoeducational Attention Control (AC)

Interventions

  • BehavioralBrief Motivational Mobile Health (mHealth) Intervention

    Participants randomized to the mHealth intervention condition will receive a five-week online program that incorporates weekly text messages. The program will begin with prompting the young adult to reflect on their journey with cannabis and to reflect on their personal goals and how cannabis is reflected in these goals and how their social network may support their goals. Additional mini-modules are included related to topics such as motivations for use, perceived norms and tracking cannabis use. Text messages will be sent weekly to return to the program to prompt reflection and support any goals the participant indicates.

  • OtherPsychoeducational Attention Control (AC)

    Participants randomized to the control group will receive a program to learn more about psychoeducational information about cannabis. They also receive psychoeducational material via text messages.

06

What researchers measure

Primary outcomes

  1. Cannabis use - typical hours high in a week

    The count of the self-reported typical number of hours high per week during the past month

    Time frame: Baseline, 3-month follow-up, 6-month follow-up

  2. Negative cannabis-related consequences

    Total sum score on the Marijuana Consequences Checklist based on number of self-reported cannabis-related consequences experienced in the past month. Higher scores indicate reporting greater number of negative cannabis-related consequences.

    Time frame: Baseline, 3-month follow-up, 6-month follow-up

Secondary outcomes

  1. Cannabis use - Number of sessions

    Self-reported number of times/sessions used cannabis on the typical day during the past month

    Time frame: Baseline, 3-month follow-up, 6-month follow-up

07

Study locations

1 site
  • University of Washington
    Seattle, Washington 98195, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07011615
Lead sponsor
University of Washington
Collaborators
National Institute on Drug Abuse (NIDA)
Responsible party
Christine Lee (Research Professor, School of Medicine: Psychiatry, University of Washington) — Principal investigator
First posted
Jun 9, 2025
Start date
Dec 8, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Jun 3, 2026

Study contacts

Christine M Lee, PhD
principal investigator · leecm@uw.edu

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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