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NCT04160702 · ClinicalTrials.gov registry record · NA

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

A NA study of Sexual Assault, sponsored by University of Nebraska Lincoln.

Completed
Registry status
NA
Development phase
57
Enrollment target
1
Study location

NCT04160702 is a NA study of Sexual Assault that has completed, run by University of Nebraska Lincoln. The registered enrollment target is 57 participants, below the 746-participant average among 12 other Sexual Assault trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04160702, a NA study of Sexual Assault, has completed, sponsored by University of Nebraska Lincoln.

COMPLETED
Registry status
NA
Development phase
57 participants
Enrollment target
1
Study location

Study 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.

Conditions Studied

Interventions

  • BEHAVIORAL Motivate-The-Bystander (MTB)

Study Locations (1)

Nebraska

  • University of Nebraska Lincoln - Lincoln

Trial Details

FieldValue
Enrollment Target 57 participants
Start Date 2019-09-27
Est. Completion 2021-02-15
Phase NA

Sponsor

University of Nebraska Lincoln

24 total trials

What the Registry Record Tells You About NCT04160702

The ClinicalTrials.gov registry entry for NCT04160702 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 57 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 746-participant average among 12 other Sexual Assault trials with a reported enrollment target (92% lower). The listed sponsor is University of Nebraska Lincoln, which has 24 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Sexual Assault appearing as the primary indexed condition, and to 1 intervention - of which Motivate-The-Bystander (MTB) is the first listed.

NCT04160702 reports 1 study location spanning 1 distinct geographic area - top geographies include Nebraska.

Frequently Asked Questions

What is clinical trial NCT04160702 about?

NCT04160702 is a clinical study titled "Using VR to Assess the Efficacy of a Motivational Interviewing Intervention to Increase Bystander Behaviors". 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 intervent...

What is the current status of trial NCT04160702?

This trial is currently completed. It is a NA study. The enrollment target is 57 participants. The study started on 2019-09-27. Estimated completion is 2021-02-15.

What conditions does trial NCT04160702 study?

This clinical trial studies the following conditions: Sexual Assault.

What interventions are being tested in trial NCT04160702?

The interventions under investigation include: Motivate-The-Bystander (MTB) (BEHAVIORAL).

Who is sponsoring clinical trial NCT04160702?

This trial is sponsored by University of Nebraska Lincoln, which has 24 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04160702 being conducted?

This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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