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Recruiting NCT07557745

uSafeUS+ App Pilot Testing

Conditions: Alcohol Consumption, Sexual Assault

Sex: All
Ages: 18 Years – 25 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 90
Sponsor: University of Florida

Location: University of Florida Gainesville Florida

Summary

The purpose of this study is to test the feasibility and acceptability of an innovative mobile application (uSafeUS+) to reduce college student drinking and sexual assault (SA) risk in real time. Following an initial period of app development, this study will use a pilot 3-arm randomized controlled trial (N = 90; 30/arm) to examine the acceptability, feasibility, and initial evidence of efficacy of the novel, expanded uSafeUS+ app, relative to the existing SA-only focused uSafeUS app (already in use on 24 college campuses), and an assessment-only control condition. Specifically, the investigators aim to answer the following research questions: 1. Do students like the app (overall and specific features)? 2. How frequently do students use the app within the 1-month exposure period? 3. What barriers and facilitators impact app use? 4. Is there evidence of increased use of protective behaviors on drinking days and over time? 5. Is there evidence of decreased drinking (amount, frequency) or SA risk on drinking days and over time? Participants will complete: * A baseline assessment * A 1-month app exposure period with daily surveys about app use on the weekends * Follow-up surveys at 1- and 2-months post-intervention.

Eligibility Criteria

Inclusion Criteria: * Participants must be between the ages of 18 and 25 years old; * Currently enrolled as a residential undergraduate student at a participating university; * Intend to reside on or near (in the same town) campus over the two-month study period * Own a smartphone/mobile device; * Have consumed at least one alcoholic beverage per week or engaged in dating or social behaviors where alcohol is present at least once a week over the past 30 days; * Intend to drink or go out at the same frequency (at least weekly) over the two-month study period Exclusion Criteria: * Unable or unwilling to provide informed consent

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07557745). StuddyBuddy aggregates publicly available trial information.