- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05486234
CARS: Cannabis and Alcohol Reduction Study (CARS)
August 11, 2026 updated by: Austin Hahn, Medical University of South Carolina
Brief Computerized Intervention for Reducing Adolescent Cannabis and Alcohol Use
The study will test a computerized treatment with subjects ages 13-17 years who are seeking treatment for alcohol and/or cannabis use.
Follow-up assessments will be conducted at one- and three-months following treatment.
Study Overview
Status
Recruiting
Study Type
Interventional
Enrollment (Estimated)
52
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Austin M Hahn, Ph.D.
- Phone Number: 854-444-9456
- Email: hahna@musc.edu
Study Locations
-
-
South Carolina
-
Charleston, South Carolina, United States, 29425
- Recruiting
- Medical University of South Carolina
-
Contact:
- Austin Hahn, Ph.D.
- Phone Number: 854-444-9456
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
13 years to 17 years (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- between the ages of 13 and 17
- be seeking treatment for either cannabis or alcohol use;
- report co-occurring alcohol and cannabis use during the past three months (i.e., participants who report using both alcohol and cannabis during the three months prior to participation in the study, regardless of if the use was simultaneous)
- have a caregiver willing to participate and provide consent.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A: Treatment Group
|
Participants will undergo a baseline assessment before completing computerized tasks.
During the baseline assessment, participants will be asked questions about alcohol and cannabis use.
We will also ask questions about the way participants think about things, past life experiences related to substance use, and questions about how participants feel about reducing their substance use.
Then, participants will complete a series computerized tasks where they will push and pull a joystick in response to images that are presented on a screen or where they will try to get a high score.
During the computerized tasks, we will also be measuring brain activity using EEG.
During the study, participants will also be asked to respond to questions about their health and behavior using an app on a smartphone or tablet using a secure program.
Participants in the Treatment Group will then complete four sessions of the modified Approach-Avoidance Task (mAAT), which aims to modify automatic approach bias.
|
|
Sham Comparator: Group B: Control Group
|
Participants will undergo a baseline assessment before completing computerized tasks.
During the baseline assessment, participants will be asked questions about alcohol and cannabis use.
We will also ask questions about the way participants think about things, past life experiences related to substance use, and questions about how participants feel about reducing their substance use.
Then, participants will complete a series computerized tasks where they will push and pull a joystick in response to images that are presented on a screen or where they will try to get a high score.
During the computerized tasks, we will also be measuring brain activity using EEG.
During the study, participants will also be asked to respond to questions about their health and behavior using an app on a smartphone or tablet using a secure program.
Participants in the Control Group will then complete four sessions of an Approach-Avoidance Task (mAAT) that does not aim to modify automatic approach bias.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in cannabis use as assessed by Timeline Followback
Time Frame: Baseline and Three-Month Follow-up
|
The TLFB is a calendar-assisted semi-structured interview that will be used to assess cannabis and alcohol use since the last assessment.
The TLFB will assess the number of days a person used cannabis over the past 90 days compared to the 90 days prior to enrolling in this study.
|
Baseline and Three-Month Follow-up
|
|
Change in alcohol use as assessed by Timeline Followback
Time Frame: Baseline and Three-Month Follow-up
|
The TLFB is a calendar-assisted semi-structured interview that will be used to assess cannabis and alcohol use since the last assessment.
The TLFB will assess the number of days a person consumed alcohol over the past 90 days compared to the 90 days prior to enrolling in this study.
|
Baseline and Three-Month Follow-up
|
|
Change in Cannabis Approach Bias (D-Score)
Time Frame: Baseline, One-Week Follow-up, and Three-Month Follow-up
|
D scores will be calculated for each participant at baseline, posttest, and three-month follow-up.
Participants' mean reaction times (RTs) during the approach cannabis trials will be subtracted from the mean avoid cannabis trial RTs.
These scores are then divided by the SD across all cannabis trials.
Positive scores indicate an approach bias for cannabis stimuli.
|
Baseline, One-Week Follow-up, and Three-Month Follow-up
|
|
Change Cannabis Approach Bias (D-Score)
Time Frame: Baseline, One-Week Follow-up, and Three-Month Follow-up
|
D scores will be calculated for each participant at baseline, posttest, and three-month follow-up.
Participants' mean reaction times (RTs) during the approach alcohol trials will be subtracted from the mean avoid alcohol trial RTs.
These scores are then divided by the SD across all alcohol trials.
Positive scores indicate an approach bias for alcohol stimuli.
|
Baseline, One-Week Follow-up, and Three-Month Follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 25, 2023
Primary Completion (Estimated)
September 30, 2026
Study Completion (Estimated)
October 1, 2026
Study Registration Dates
First Submitted
August 1, 2022
First Submitted That Met QC Criteria
August 2, 2022
First Posted (Actual)
August 3, 2022
Study Record Updates
Last Update Posted (Actual)
August 13, 2026
Last Update Submitted That Met QC Criteria
August 11, 2026
Last Verified
August 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 00106723
- 1K23DA050800-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.