An Evaluation of an Online Sexual Assault Resistance Program (IDEA3)

NCT06058455 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1920

Last updated 2025-10-21

No results posted yet for this study

Summary

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.

Conditions

  • Sexual Assault

Interventions

BEHAVIORAL

IDEA3 Sexual Assault Resistance Intervention

Internet-delivered EAAA (IDEA3), adapted from an in-person sexual assault resistance education intervention: Enhanced Assess, Acknowledge, Act (EAAA) intervention that was found in a randomized trial to reduce sexual assault victimization by about 50% at follow-up. IDEA3 designed for female identifying university students and focuses on resisting sexual assault committed by males in 4, 3-hour units: 1-ASSESS builds ability to detect risk with male acquaintances and develop risk reduction strategies. 2-ACKNOWLEDGE explores overcoming emotional barriers preventing women from acknowledging risk and employing effective resistance strategies with males. 3-ACT shows effectiveness of resistance strategies and teaches verbal and physical self-defense in common situations. 4-RELATIONSHIPS \& SEXUALITY adapts the Our Whole Lives curriculum to increase women's comfort in talking about sex/sexuality and identify sexual values/desires.

BEHAVIORAL

Consent Workshop

Participant pairs assigned to the control arm will receive a 60-minute session consisting of a 60-min interactive, virtual consent workshop. The workshop will include information on a) what consent is, including the idea that consent is about bodily autonomy and applies to interactions beyond sex, b) how to give and ask for consent, and c) examples of what it looks like to ask for and give/not give consent. This presentation will be given by a well-trained Research Assistant.

Sponsors & Collaborators

  • University of Windsor

    collaborator OTHER
  • University of Nebraska

    collaborator OTHER
  • University of Guelph

    collaborator OTHER
  • Tufts University

    collaborator OTHER
  • University of Central Florida

    collaborator OTHER
  • University of Michigan

    collaborator OTHER
  • University of Maryland, College Park

    lead OTHER

Principal Investigators

  • Sarah M Peitzmeier, PhD · University of Maryland

  • Charlene Y Senn, PhD · University of Windsor

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
17 Years
Max Age
24 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-10-02
Primary Completion
2027-09-01
Completion
2027-12-31

Countries

  • United States
  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06058455 on ClinicalTrials.gov