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Behavioral Intervention

Bystander Intervention Programs for Preventing Sexual Violence (MAP Trial)

N/A
Recruiting
Led By David DiLillo, PhD
Research Sponsored by University of Nebraska Lincoln
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up months 0-9

Summary

This trial aims to test different methods to encourage people to intervene in situations where others are at risk. They will compare the effectiveness of a bystander intervention program alone, the program with an alcohol component,

Who is the study for?
This trial is for individuals aged 18-25 who are heavy drinkers, fluent in English, and from Lancaster or nearby counties in Nebraska. Participants must be willing to follow study procedures and have signed a consent form.
What is being tested?
The study compares three approaches: 'Motivate-the-Bystander' (MTB) protocol alone, MTB with an added focus on reducing alcohol use ('MTB+Alcohol'), and a control condition aimed at stress reduction. It evaluates the effectiveness of these methods in promoting intervention behaviors during sexual risk situations and reducing alcohol consumption.
What are the potential side effects?
Since this trial involves behavioral interventions like online measures, virtual reality simulations, and diary surveys rather than medical treatments, traditional side effects are not applicable. However, participants may experience discomfort discussing sensitive topics.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~months 0-9
This trial's timeline: 3 weeks for screening, Varies for treatment, and months 0-9 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Alcohol use
Daily self-reports of bystander behavior
Observational bystander behavior

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Placebo Group
Group I: Motivate-the-Bystander+AlcoholExperimental Treatment1 Intervention
A Zoom-based motivational interviewing prevention program that enhances knowledge, motivation, and skills for reduced alcohol use and increased bystander behaviors.
Group II: Motivate-the-BystanderActive Control1 Intervention
A Zoom-based motivational interviewing prevention program that enhances knowledge, motivation, and skills for increased bystander behaviors.
Group III: Attention-only controlPlacebo Group1 Intervention
A Zoom-based stress reduction program in which progressive muscle relaxation and other techniques are introduced and practiced.

Find a Location

Who is running the clinical trial?

National Institute on Alcohol Abuse and Alcoholism (NIAAA)NIH
839 Previous Clinical Trials
1,083,321 Total Patients Enrolled
University of Nebraska LincolnLead Sponsor
37 Previous Clinical Trials
12,440 Total Patients Enrolled
David DiLillo, PhDPrincipal InvestigatorUniversity of Nebraska Lincoln
Sarah J Gervais, PhDPrincipal InvestigatorUniversity of Nebraska Lincoln
~294 spots leftby May 2026