Efficacy of a Web-based Sexual Violence Risk Reduction Program for Female College Students

Completed · Not applicable

Conditions studied: Sexual Violence

In brief

This study evaluates the efficacy of a web-based program for female college freshmen ("RealConsent") in reducing their risk of sexual violence victimization. Half the participants will receive RealConsent-F and half will receive an attention-placebo control ("Stress and Mood Management").

Key facts

Study ID

NCT03726437

Run by

Georgia State University

People needed

881

Starts

2018-10-17

Expected to finish

2019-11-01

Last updated by the study team

2023-02-13

Who can join

Age: 18 and older, up to 20. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• female, aged 18-20 years, full-time freshmen, matriculated at Georgia State University, Emory University, or University of Georgia, and single (i.e., not in a committed dating relationship).

You may not qualify if…

• other education levels, married, and/or graduate status

Where it is running

• Georgia State University — Atlanta, Georgia, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.