Using VR to Assess the Efficacy of a Motivational Interviewing Intervention to Increase Bystander Behaviors

Sponsor
University of Nebraska Lincoln (Other)
Overall Status
Completed
CT.gov ID
NCT04160702
Collaborator
University of Nebraska (Other)
57
1
2
16.7
3.4

Study Details

Study Description

Brief Summary

With the present project, we will a evaluate a new, motivational interviewing (MI) intervention for increasing bystander behaviors to prevent sexual violence. In the intervention, motivational interviewing will be used to build each participant's unique motivation for engaging in bystander intervention behaviors. To assess the efficacy of the intervention, we will utilize the Bystanders in Sexual Assault Virtual Environments (B-SAVE), a virtual reality measure of bystander behaviors, along with self-report measures examining relevant bystander behaviors and attitudes. We will also examine key moderators of intervention efficacy to provide valuable knowledge (e.g., whom the intervention is most effective for) for further tailoring of the intervention.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Motivate-The-Bystander (MTB)
N/A

Detailed Description

This study will provide a comprehensive examination of Motivate-The-Bystander and provide information about whom the intervention is most effective for. Specifically, at T1, participants will be randomly assigned to the MTB condition, a motivational interviewing intervention designed to increase participants' bystander intervention behaviors, or an assessment only control condition. All participants will complete a battery of self-report measures, including our three proposed moderators (gender, alcohol use, and rape myth acceptance). Participants assigned to the MTB condition will also engage in a motivational interviewing intervention designed to build each participant's unique motivation for engaging in bystander intervention behaviors. Approximately two months later, at T2, participants will complete a battery of self-report measures assessing their bystander behaviors and attitudes over the past two months. Then, all participants will complete the B-SAVE, where they provide open ended verbal responses to a series of sexually risky and non-risky interactive scenes they witness in the virtual environment.

Study Design

Study Type:
Interventional
Actual Enrollment :
57 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
Individuals will be randomly assigned to complete either a motivational interviewing intervention to increase bystander behaviors or an assessment only control condition. The outcome variables are post-treatment bystander behaviors, measured through both self-report measures and a virtual realty assessment of bystander behaviors. The primary analyses will consist of a series of multiple regressions with intervention group (0 = control, 1 = MI training) interacting with each of the moderators to predict post-treatment bystander behaviors (self-reported and B-SAVE).Individuals will be randomly assigned to complete either a motivational interviewing intervention to increase bystander behaviors or an assessment only control condition. The outcome variables are post-treatment bystander behaviors, measured through both self-report measures and a virtual realty assessment of bystander behaviors. The primary analyses will consist of a series of multiple regressions with intervention group (0 = control, 1 = MI training) interacting with each of the moderators to predict post-treatment bystander behaviors (self-reported and B-SAVE).
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Using Virtual Reality to Assess the Efficacy of a Motivational Interviewing Intervention to Increase Bystander Behaviors
Actual Study Start Date :
Sep 27, 2019
Actual Primary Completion Date :
Feb 15, 2021
Actual Study Completion Date :
Feb 15, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Motivate-The-Bystander

Participants assigned to the MTB condition arm.

Behavioral: Motivate-The-Bystander (MTB)
MTB is a motivational interviewing intervention designed to increase bystander intervention behaviors. During MTB, participants will discuss their knowledge and experiences with bystander intervention. Participants will then create a plan to increase their bystander intervention behaviors in the future. The interviewer will utilize a variety of motivational interviewing techniques to help guide the conversation towards change (e.g., asking questions in an open-ended manner, reflecting participants' personal values).

No Intervention: Assessment only control condition

Participants assigned to the assessment only condition arm.

Outcome Measures

Primary Outcome Measures

  1. Bystander in Sexual Assault Virtual Environment (BSAVE) [Two months after the intervention]

    The primary outcome measure consists of participants' open ended verbal responses to a series of sexually risky and non-risky interactive scenes they witness while in the virtual house party.

Secondary Outcome Measures

  1. Bystander Attitudes Scale [Two months after the intervention]

    A self-report measure assessing participants' bystander related attitudes.

  2. Bystander Behavior Scale [Two months after the intervention]

    A self-report measure assessing participants' actual bystander behaviors over the past two months.

  3. Bystander Efficacy Scale [Two months after the intervention]

    A self-report measure assessing participants' confidence in their ability to engage in future bystander behaviors.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 25 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Ages 18-25, English speaking
Exclusion Criteria:
  • Non English speaking.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Nebraska Lincoln Lincoln Nebraska United States 68588

Sponsors and Collaborators

  • University of Nebraska Lincoln
  • University of Nebraska

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Nebraska Lincoln
ClinicalTrials.gov Identifier:
NCT04160702
Other Study ID Numbers:
  • 19260
First Posted:
Nov 13, 2019
Last Update Posted:
Mar 19, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Nebraska Lincoln

Study Results

No Results Posted as of Mar 19, 2021