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A Social Media Intervention for Risky Drinking

Not Applicable
Completed
Conditions
Drinking Behavior
Interventions
Behavioral: Social media messaging
Registration Number
NCT04721925
Lead Sponsor
University of Michigan
Brief Summary

This study is being completed to pilot prevention methods to promote wellness and reduce risky behaviors, including the use of substances such as alcohol and other drugs. This study will help the study team learn about ways of delivering this information that is both appealing and helpful to young adults.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
102
Inclusion Criteria
  • Reside in the United States of America (USA)
  • Be able to read English, view, and click on a social media advertisement.
  • Self-reported past-month high-intensity drinking (HID)
  • Regular Snapchat use (at least 3 days/week).
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Exclusion Criteria
  • If they fail identity verification based on: 1) internet protocol address (IP), 2) survey time completion, 3) repeat attempts, and 4) survey responses.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Social media messagingSocial media messagingHealth coaching via social media for 8 weeks
Primary Outcome Measures
NameTimeMethod
Feasibility of the Intervention (Completion)8 weeks

% of participants who remain connected to intervention account at 8 weeks (end of intervention) There are no statistical analyses because pre-registered primary outcomes are descriptive in nature.

Intervention Acceptability2 months

Study-specific acceptability rating completed by participants (% with a positive rating, higher % is better):

Item wording: Overall, how did you feel about Snapchatting with the team? Response options: Disliked it a lot, Disliked it, Neutral, Liked it/Liked it a lot

There are no statistical analyses because pre-registered primary outcomes are descriptive in nature.

Feasibility of the Intervention (Engagement)During the 8 week intervention delivery period

% of participants engaging in the intervention (at least one reply) There are no statistical analyses because pre-registered primary outcomes are descriptive in nature.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Michigan

🇺🇸

Ann Arbor, Michigan, United States

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