An Evaluation of an Online Sexual Assault Resistance Program (IDEA3) (NCT06058455)
A Randomized Controlled Trial of the Efficacy of IDEA3 - An Evidence-based Sexual Assault Resistance Intervention for Undergraduate Women Adapted for Internet Delivery
🩺 Plain-English Summary (8th-Grade Level)
The goal of this randomized trial is to test whether the Internet-Delivered Enhanced Assess, Acknowledge, Act (IDEA3) sexual assault resistance education intervention reduces sexual violence victimization in undergraduate women. Participants in the intervention group will be asked to attend four three-hour group sessions of a sexual assault resistance program called IDEA3 with a partner, as well as fill out a number of surveys. Participants in the control group will be asked to attend a one-hour consent workshop with a partner and fill out surveys. Researchers will compare sexual assault victimization between the groups in the one year following the intervention.
Who can join: Review the eligibility criteria below.
Location: University of Central Florida — Orlando, Florida
Age range: 17 Years to 24 Years
🧪 Interventions in This Study
- IDEA3 Sexual Assault Resistance Intervention (BEHAVIORAL)
- Consent Workshop (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (6 Sites)
- University of Central Florida — Orlando, Florida
- University of Maryland — College Park, Maryland
- University of Michigan — Ann Arbor, Michigan
- University of Nebraska - Lincoln — Lincoln, Nebraska
- University of Guelph — Guelph, Ontario
- University of Windsor — Windsor, Ontario
📞 Contact the Study Coordinator
Phone: (301) 405-2526
Email: speitzme@umd.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.