In-School Evaluation of Bystander: A Game-Based Intervention for Sexual Violence Prevention

February 21, 2023 updated by: University of Chicago
The investigators have developed a game-based sexual violence prevention program that uses a bystander intervention approach. This program is called Bystander and was designed for use with high school students in grades 9-12. The goal of this research is to evaluate the efficacy and feasibility of Bystander when implemented in a school setting. The research will capture data on knowledge about sexual violence and harassment, as well as attitudes, self-efficacy, perceived social norms and behavioral intentions around bystander behaviors. This research will consist of a baseline survey, program participation, a immediate post-program survey, and a 3-month follow up survey with youth participants. It will also involve qualitative in-depth interviews with school staff and administration about the program.

Study Overview

Detailed Description

Using the investigators' experience in game-based learning, digital media, behavior theory, and adolescent sexual and reproductive health, the investigators have developed a digital game-based sexual violence prevention program-Bystander-to be used with high school students to teach them about prosocial bystander behaviors and decrease acceptance of common rape myths. The goal of this research is to evaluate the efficacy and feasibility of Bystander when implemented in a school setting.

This study will evaluate Bystander, a four-module intervention program. Each module is designed to last one school class period. It includes 20 minutes of individual gameplay through an interactive narrative featuring prosocial bystander behaviors and discussions dispelling rape myths. Each module also includes facilitated class discussion about the topics covered that day.

The research team will conduct a pre/post efficacy and feasibility study that will capture data through a pre-, immediate post-, and 3-month follow up survey on knowledge about sexual violence and harassment, as well as attitudes, self-efficacy, perceived social norms and behavioral intentions around bystander behaviors (all measured at pre-, immediate post- and follow-up time points). It will also capture demographic information and previous bystander behaviors at baseline. It will finally involve qualitative in-depth interviews with school staff and administration about the program.

Study Type

Interventional

Enrollment (Actual)

601

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Chicago, Illinois, United States, 60637
        • University of Chicao

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

13 years to 19 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age 13-19 years
  • A student in grades 9-12 at one of three identified study site schools
  • Able to speak and read English at a 7th grade level
  • Provide informed consent and express willingness to complete the follow-up survey.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
Two schools (all students grades 9-12) will serve as the intervention group.Participants will complete a baseline survey that will take no longer than 30 minutes. Afterwards, a trained facilitator will delivery a game-based bystander intervention program aimed at teaching students the knowledge and skills to prevent or intervene in instances in sexual harassment and violence among peers. This will last for 4 class periods (approximately 45 minutes each period, 180 minutes total). Afterwards, participants will complete an immediate post-program survey lasting no more than 30 minutes. Three months later, students will fill out an a follow up survey lasting no more than 30 minutes. School staff and administrators will be interviewed to gather their insights on the program's feasibility and acceptability.
A game-based, high school age-appropriate program delivered by trained facilitators for sexual violence and harassment intervention
Placebo Comparator: Delayed Control

One school (all students grades 9-12) will serve as a delayed control group. Participants will complete a baseline survey that will take no longer than 30 minutes. Afterwards, a trained facilitator will delivery a game-based health program unrelated to sexual health, sexual violence, sexual harassment, and bystander behaviors. This will last for 4 class periods (approximately 45 minutes each period, 180 minutes total). Afterwards, participants will complete an immediate post-program survey lasting no more than 30 minutes. Three months later, students will fill out an a follow up survey lasting no more than 30 minutes.

After completing the follow-up survey, this group will follow the same procedures to deliver the bystander program and capture data outlined for the intervention group.

A game-based, high school age-appropriate program delivered by trained facilitators for sexual violence and harassment intervention
A game-based, high school age-appropriate program delivered by trained facilitators to teach students about meningitis.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in bystander behavioral intention
Time Frame: pre, immediate post, 3 month follow up
measured via validated 11-item Bystander Attitude Scale-Revised by McMahon et al 2014
pre, immediate post, 3 month follow up
change in attitudes towards sexual violence and harassment
Time Frame: pre, immediate post, 3 month follow up
measured via validated 22-item Modified Illinois Rape Myth Acceptance Scale by McMahon 2011
pre, immediate post, 3 month follow up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in knowledge of sexual harassment and violence
Time Frame: pre, immediate post, 3 month follow up
measured via validated 7-item Legal Knowledge Scale (Maxwell 2003)
pre, immediate post, 3 month follow up
change in knowledge of sexual harassment and violence
Time Frame: pre, immediate post, 3 month follow up
measured via Knowledge of Sexual Violence and Harassment index (Banyard et al 2005)
pre, immediate post, 3 month follow up
change in perceived social norms for bystander behaviors
Time Frame: pre, immediate post, 3 month follow up
measured via validated Social Norms Scale from Gidycz et al 2011
pre, immediate post, 3 month follow up
change in self-efficacy for bystander behaviors
Time Frame: pre, immediate post, 3 month follow up
measured via validated 14-item Bystander Efficacy Scale by Banyard et al 2004
pre, immediate post, 3 month follow up
change in self-efficacy for bystander behaviors
Time Frame: pre, immediate post, 3 month follow up
measured via validated 10-item MVP Efficacy Scale by Ward 2001
pre, immediate post, 3 month follow up
change in decisional balance for bystander behaviors
Time Frame: pre, immediate post, 3 month follow up
measured via validated 10-item Bystander Decisional Balance Scale by Banyard 2004
pre, immediate post, 3 month follow up
change in normative beliefs around sexual violence
Time Frame: pre, immediate post, 3 month follow up
measured via validated 8-item Reaction to Offensive Language Scale--Comfort Subscale by Loh 2005
pre, immediate post, 3 month follow up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Melissa Gilliam, MD, MPH, University of Chicago

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 1, 2016

Primary Completion (Actual)

October 1, 2017

Study Completion (Actual)

October 1, 2017

Study Registration Dates

First Submitted

September 28, 2016

First Submitted That Met QC Criteria

September 28, 2016

First Posted (Estimate)

September 29, 2016

Study Record Updates

Last Update Posted (Estimate)

February 23, 2023

Last Update Submitted That Met QC Criteria

February 21, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • IRB15-1404

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Bystander Behavioral Intentions

Clinical Trials on Bystander, a game-based bystander intervention program

Subscribe