Testing a Novel Instagram Intervention for Heavy Alcohol Use

May 14, 2024 updated by: Emily Grekin

Testing a Novel Instagram Intervention for Heavy Alcohol Use: A Randomized Controlled

This project aims to test the efficacy of an Instagram-based intervention for reducing heavy alcohol use. More specifically, the investigators will use a randomized controlled design to analyze differences in alcohol use and alcohol-related outcomes (e.g., alcohol-related consequences, etc.) as well as differences in the use of protective behavioral strategies and mindfulness practices. Participants (80 Prolific users who report binge drinking) will be randomly assigned to 1 of 3 conditions: intervention or control. Those who are randomized to the intervention condition will be invited to follow study Instagram pages, and those who are randomized to the control condition will be invited to complete the assessments only. The investigators hypothesize that there will be greater reductions in alcohol use, frequency, and consequences and greater frequency of use of mindfulness exercises and protective behavioral strategies among those in the intervention condition as compared to those in the control condition.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

80

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

Study Locations

    • Michigan
      • Detroit, Michigan, United States, 48202
        • 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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Ages 18-30
  • Report regular Instagram usage (i.e., at least a few times a week)
  • Report having met the NIAAA's criteria for a binge-drinking episode (4+ drinks in a sitting for cisgender women, 5+ drinks in a sitting for all other genders) at least twice a month for the past three month

Exclusion Criteria:

  • No exclusion 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: Control
Experimental: Instagram Intervention
The intervention consists of a study Instagram page, which will post intervention content every day for 42 days.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Frequency of Past-month Alcohol Use Using the Computer-Administered Timeline Follow-Back
Time Frame: Given pre-intervention and at 10-week follow-up
The investigators will analyze differences in the amount of days spent drinking.
Given pre-intervention and at 10-week follow-up
Change in Quantity of Past-month Alcohol Use Using the Computer-Administered Timeline Follow-Back
Time Frame: Given pre-intervention and at 10-week follow-up
The investigators will analyze differences in amount of past-month alcohol use and the amount of past-month binge-drinking episodes.
Given pre-intervention and at 10-week follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Frequency of Protective Behavioral Strategy Use Using the Protective Drinking Practices Scale
Time Frame: Given pre-intervention and at 10-week follow-up
The investigators will analyze the difference in frequency of recent protective behavioral strategy use using the Protective Drinking Practices Scale (minimum score = 20, maximum score = 120, and higher scores indicate a better outcome).
Given pre-intervention and at 10-week follow-up
Change in the Amount of Recent Alcohol Consequences Using the Brief Young Adult Consequences Scale
Time Frame: Given pre-intervention and at 10-week follow-up
The investigators will analyze the difference in amount of consequences related to alcohol use using the Brief Young Adult Consequences Scale (minimum score = 0, maximum score = 24, and higher scores indicate a worse outcome).
Given pre-intervention and at 10-week follow-up
Change in Frequency of Mindfulness Practice Use Using the Mindfulness Awareness Scale
Time Frame: Given pre-intervention and at 10-week follow-up
The investigators will analyze the difference in frequency of use of mindfulness practices using the Mindfulness Awareness Scale (minimum score = 15, maximum score = 90, and higher scores indicate a better outcome).
Given pre-intervention and at 10-week follow-up
Change in Readiness to Change Drinking Behavior Using the Readiness to Change Questionnaire
Time Frame: Given pre-intervention and at 10-week follow-up
The investigators will analyze the difference in reported readiness to change drinking behavior using the Readiness to Change Questionnaire (minimum score = 12, maximum score = 84, and higher scores indicate a better outcome).
Given pre-intervention and at 10-week follow-up
Participant Subjective Reactions Using Likert Scales
Time Frame: Given at 10-week follow-up
The investigators will ask participants to rate the intervention content on acceptability dimensions created specifically for this study (i.e., relevance, empathy, interest, helpfulness, respectfulness, personalization). On a given domain, minimum score = 1, maximum score = 5, and higher scores indicate better outcomes.
Given at 10-week follow-up
Participant Subjective Reactions Using Simple Yes/No Questions
Time Frame: Given at 10-week follow-up
The investigators will ask participants to rate how the intervention has qualitatively impacted them using simple yes/no questions (i.e., if they remember seeing certain posts, if the posts made them think about their drinking, affected their sense of community, etc.).
Given at 10-week follow-up

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 (Estimated)

May 20, 2024

Primary Completion (Estimated)

September 30, 2024

Study Completion (Estimated)

September 30, 2024

Study Registration Dates

First Submitted

April 10, 2024

First Submitted That Met QC Criteria

May 14, 2024

First Posted (Actual)

May 17, 2024

Study Record Updates

Last Update Posted (Actual)

May 17, 2024

Last Update Submitted That Met QC Criteria

May 14, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • IRB-23-11-6344

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

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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