- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06593483
Increasing Effectiveness of an Alcohol Use Reduction Exercise Using Self-Talk Videos
November 6, 2025 updated by: Emily Grekin, Wayne State University
The goal of the current study is to develop and test an innovative, low-burden method of post-intervention contact that is based on principles of motivational interviewing and the elicitation of change talk.
Participants will be randomly assigned to an assessment only control group, a standard BMI group or a BMI + video group.
Participants in the BMI and BMI + video groups will complete a semi-structured, motivational intervention.
Following the intervention, participants in the BMI + video group will be asked to create a personalized video in which they speak to their future self and describe their reasons for wanting to reduce their alcohol use and their commitment to change.
Doctoral level psychology graduate students will assist participants in idea generation and creation of the post-intervention video.
Video group participants will then be sent their personalized videos 21 days after the baseline session, a time when motivation to reduce drinking often begins to wane.
It is hypothesized that participants in the BMI + video group will rate the video exercise as helpful, encouraging, and easy to complete.
It is further hypothesized that, over the 6-week intervention period, (1) participants in the BMI + video group will reduce their alcohol use more than those in the standard BMI and control groups and (2) participants in the standard BMI group will reduce their alcohol use more than those in the control group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
120
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 Locations
-
-
Michigan
-
Detroit, Michigan, United States, 48201
- Wayne State University
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Meets National Institute on Alcohol Abuse and Alcoholism criteria for heavy drinking
- 18 year or older
- Accessibility to internet and laptop with camera and microphone
Exclusion Criteria:
- Failure to meet inclusion criteria
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Assessment Only
|
|
|
Active Comparator: Motivational Interview Only
|
Participants will engage in an interview based in motivational interviewing
|
|
Experimental: Motivational Interview Plus Video
|
Participants will engage in an interview based in motivational interviewing techniques and then record a self talk video discussing their goals and reasons for reducing their drinking.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Alcohol Consumption
Time Frame: 6 weeks post intervention
|
6 weeks post intervention
|
|
|
Motivation to Change Rating Scale
Time Frame: 6 weeks post intervention
|
This outcome measure asks: On a scale of 1 to 5, how likely are you to reduce your drinking over the next week, month, and year.
In this scale 1 represents not at all likely and 5 represents extremely likely.
|
6 weeks post intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rating Scales Assessing Satisfaction with the Intervention
Time Frame: 6 weeks post intervention
|
This outcome measure asks participants to rate their experience with the intervention on a number of dimensions (e.g.
empathic, personalized).
Additionally, video participants are asked to rate the extent to which they experienced different emotions (e.g.
anger, proudness) while watching their video recording.
Responses range from not at all to extremely.
|
6 weeks post intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 15, 2024
Primary Completion (Actual)
November 26, 2024
Study Completion (Actual)
November 26, 2024
Study Registration Dates
First Submitted
September 3, 2024
First Submitted That Met QC Criteria
September 9, 2024
First Posted (Actual)
September 19, 2024
Study Record Updates
Last Update Posted (Actual)
November 10, 2025
Last Update Submitted That Met QC Criteria
November 6, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 23-10-6241
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.
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