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A Web-based Bystander Education Program (RealConsent)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01903876
Recruitment Status : Completed
First Posted : July 19, 2013
Results First Posted : July 23, 2014
Last Update Posted : July 23, 2014
Centers for Disease Control and Prevention
Information provided by (Responsible Party):
Laura F Salazar, Emory University

Brief Summary:
This is a study to determine whether a theoretically-driven web-based 3-hour intervention designed for male college students called RealConsent is effective in increasing prosocial intervening behaviors and in preventing sexual violence perpetration. Sexual violence programs for this population have been implemented for decades in the United States, but a program that is web-based and incorporates the bystander education model has never been implemented or tested. In this study, male college students will be recruited online, enrolled and randomly assigned to RealConsent or to a comparison condition. Prior to the intervention, investigators will ask questions about their intervening and sexually coercive behaviors and other theoretical and empirical factors related to the study outcomes. Investigators will survey the young men again at post-intervention, and at 6-months follow-up to determine whether young men in the RealConsent program intervened more often and engaged in less sexual violence compared to young men in the comparison condition. The main hypotheses are: (1) college men in the RealConsent program will report more instances of prosocial intervening; and (2) college men in the RealConsent program will report less sexual violence against women.

Condition or disease Intervention/treatment Phase
Sexual Violence Behavioral: Bystander & Sexual Violence Prevention Behavioral: General Health Promotion Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 743 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Preventing Violence Against Women: A Web-based Approach
Study Start Date : February 2010
Actual Primary Completion Date : May 2011
Actual Study Completion Date : May 2011

Arm Intervention/treatment
Placebo Comparator: General Health promotion
A 3-hour general mental health web-based program.
Behavioral: General Health Promotion
This general health promotion web-based program is 3-hours and provides a range of activities related to reducing day-to day stress and alleviating anxiety through meditation and exercise.
Other Name: Stress & Mood Management

Experimental: Bystander & Sexual Violence Prevention
A 3-hour web-based program designed to teach male college student bystanders to intervene.
Behavioral: Bystander & Sexual Violence Prevention
This 3-hour web-based program consists of six 30-minute modules that are interactive and range in number of segments (1-14) and types of activities. Each of the modules involves interactivity, didactic activities and two episodes of a serial drama, which allows for the modeling of positive behaviors and illustrate both positive and negative outcome expectations for intervening and for perpetrating abuse against women. Behaviors modeled include communicating with female sex partners, obtaining informed consent to have sex, and intervening to prevent abuse from taking place.
Other Name: RealConsent

Primary Outcome Measures :
  1. Prosocial Intervening Behavior [ Time Frame: 6 months ]
    This scale is the Reactions to Offensive Language and Behavior (ROLB) index that measures whether or not men confronted inappropriate behaviors of other men. We used the 7-item self-behavior subscale plus an additional 8 items, which directly reflected the content of RealConsent. A series of 15 potential intervening situations were presented and participants were asked to indicate whether they had experienced this situation in past 6 months (yes/no), and whether they had intervened (yes/no). The scale ranged from 0% (did not intervene anytime) to 100% (intervened every time).

Secondary Outcome Measures :
  1. Sexual Violence Perpetration [ Time Frame: 6 months ]
    This scale is the Conflict Tactics Scale revised, Sexual Coercion Subscale and assessed the number of sexually coercive/violent behaviors engaged in during the past 6 months. The index ranges from 0 (no engagement in any sexual violence) to 7 (engaged in all 7 sexually violent behaviors).

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 24 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Student matriculated at Georgia State University
  • Male
  • 18 to 24
  • Undergraduate
  • Self-identify as heterosexual or bisexual

Exclusion Criteria:

  • Graduate student
  • Self-identify as homosexual

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01903876

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United States, Georgia
Georgia State University
Atlanta, Georgia, United States, 30303
Sponsors and Collaborators
Emory University
Centers for Disease Control and Prevention
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Principal Investigator: Laura F Salazar, PhD Emory University
Publications automatically indexed to this study by Identifier (NCT Number):
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Responsible Party: Laura F Salazar, Assistant Professor, Emory University Identifier: NCT01903876    
Other Study ID Numbers: IRB00000472
R49CE000892 ( U.S. NIH Grant/Contract )
EmoryVAW ( Other Identifier: Other )
First Posted: July 19, 2013    Key Record Dates
Results First Posted: July 23, 2014
Last Update Posted: July 23, 2014
Last Verified: July 2014