Reducing Alcohol Use and Sexual Dysfunction in Survivors of Sexual Trauma

Completed · Not applicable

Conditions studied: Alcohol Use, Unspecified, Sexual Dysfunction, Sexual Assault

In brief

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 facts

Study ID
NCT05599620
Run by
Lifespan
People needed
86
Starts
2023-02-14
Expected to finish
2026-03-30
Last updated by the study team
2026-04-29

Who can join

Age: 18 and older, up to 24. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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