- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02919098
In-School Evaluation of Bystander: A Game-Based Intervention for Sexual Violence Prevention
Study Overview
Status
Conditions
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Illinois
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Chicago, Illinois, United States, 60637
- University of Chicao
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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 |
|---|---|
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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.
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A game-based, high school age-appropriate program delivered by trained facilitators for sexual violence and harassment intervention
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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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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change in bystander behavioral intention
Time Frame: pre, immediate post, 3 month follow up
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measured via validated 11-item Bystander Attitude Scale-Revised by McMahon et al 2014
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pre, immediate post, 3 month follow up
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change in attitudes towards sexual violence and harassment
Time Frame: pre, immediate post, 3 month follow up
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measured via validated 22-item Modified Illinois Rape Myth Acceptance Scale by McMahon 2011
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pre, immediate post, 3 month follow up
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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
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measured via validated 7-item Legal Knowledge Scale (Maxwell 2003)
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pre, immediate post, 3 month follow up
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change in knowledge of sexual harassment and violence
Time Frame: pre, immediate post, 3 month follow up
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measured via Knowledge of Sexual Violence and Harassment index (Banyard et al 2005)
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pre, immediate post, 3 month follow up
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change in perceived social norms for bystander behaviors
Time Frame: pre, immediate post, 3 month follow up
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measured via validated Social Norms Scale from Gidycz et al 2011
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pre, immediate post, 3 month follow up
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change in self-efficacy for bystander behaviors
Time Frame: pre, immediate post, 3 month follow up
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measured via validated 14-item Bystander Efficacy Scale by Banyard et al 2004
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pre, immediate post, 3 month follow up
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change in self-efficacy for bystander behaviors
Time Frame: pre, immediate post, 3 month follow up
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measured via validated 10-item MVP Efficacy Scale by Ward 2001
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pre, immediate post, 3 month follow up
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change in decisional balance for bystander behaviors
Time Frame: pre, immediate post, 3 month follow up
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measured via validated 10-item Bystander Decisional Balance Scale by Banyard 2004
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pre, immediate post, 3 month follow up
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change in normative beliefs around sexual violence
Time Frame: pre, immediate post, 3 month follow up
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measured via validated 8-item Reaction to Offensive Language Scale--Comfort Subscale by Loh 2005
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pre, immediate post, 3 month follow up
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Melissa Gilliam, MD, MPH, University of Chicago
Publications and helpful links
General Publications
- Maxwell, Christopher D., Amanda L. Robinson, and Lori A. Post.
- McMahon, Sarah, and G. Lawrence Farmer.
- McMahon S, Allen CT, Postmus JL, McMahon SM, Peterson NA, Lowe Hoffman M. Measuring bystander attitudes and behavior to prevent sexual violence. J Am Coll Health. 2014;62(1):58-66. doi: 10.1080/07448481.2013.849258.
- Gidycz CA, Orchowski LM, Berkowitz AD. Preventing sexual aggression among college men: an evaluation of a social norms and bystander intervention program. Violence Against Women. 2011 Jun;17(6):720-42. doi: 10.1177/1077801211409727. Epub 2011 May 12.
- Banyard, Victoria L., Elizabethe G. Plante, and Mary M. Moynihan.
- Ward CL, Flisher AJ, Zissis C, Muller M, Lombard C. Exposure to violence and its relationship to psychopathology in adolescents. Inj Prev. 2001 Dec;7(4):297-301. doi: 10.1136/ip.7.4.297.
- Loh C, Gidycz CA, Lobo TR, Luthra R. A prospective analysis of sexual assault perpetration: risk factors related to perpetrator characteristics. J Interpers Violence. 2005 Oct;20(10):1325-48. doi: 10.1177/0886260505278528.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IRB15-1404
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