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Reducing Alcohol Use and Sexual Dysfunction in Survivors of Sexual Trauma
Sponsor: Lifespan
Summary
The goal of this clinical trial is to develop and evaluate the preliminary efficacy of an intervention to address alcohol use, sexual distress, and sexual assault risk among college women with a history of sexual victimization. The main questions it aims to answer are: 1) what is the feasibility of the recruitment method, research design, interventionist training methods, and delivery of the intervention; 2) does the intervention, relatively to control, the 2- and 4-month follow-up produces reductions in the quantity/frequency of alcohol use and heavy drinking, sexual distress, and sex-related drinking motives, and sexual revictimization. Participants will engage in both individual and group based intervention for alcohol use, sexual distress, and sexual assault risk. Follow-up assessments are completed at 2- and 4-months following program completion. The intervention is compared to a wait list control group who will have the opportunity to complete the program after completing the 4-month follow up.
Key Details
Gender
FEMALE
Age Range
18 Years - 24 Years
Study Type
INTERVENTIONAL
Enrollment
90
Start Date
2023-02-14
Completion Date
2026-04-30
Last Updated
2026-01-07
Healthy Volunteers
Yes
Interventions
AWARE
AWARE addresses alcohol use, sexual distress, and sexual assault risk among college women with a history of sexual victimization.
Locations (1)
Rhode Island Hospital
Providence, Rhode Island, United States