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Exploring Virtual Reality Adventure Training Exergaming — V-RATE  

Depression Clinical Trial

Official title:
Exploring Virtual Reality Adventure Training Exergaming (V-RATE) on Women Veterans' Health Outcomes

Clinical Trial Summary

The current project aims to design and implement an 8-week Virtual Reality Adventure Therapy Exergaming (V-RATE) intervention focused on women veterans. A randomized controlled trial using a repeated measure design with a 1-month follow-up assessment will be employed to examine effects on physical and mental health outcomes.

Clinical Trial Description

The current project aims to design and implement an 8-week Virtual Reality Adventure Therapy Exergaming (V-RATE) intervention focused on women veterans. A randomized controlled trial using a repeated measure design with a 1-month follow-up assessment will be employed. The project addresses two specific aims: Aim 1. To examine the effects of an 8-week V-RATE intervention on physical health (i.e., BMI, physical activity, sedentary behavior, heart rate variability) among women veterans. We hypothesize that after controlling for socio-demographic variables and physical activity history, individuals in the V-RATE group would exhibit more improvement in the physical health indicators after the intervention compared to individuals in the control group. We further hypothesize gains would be maintained or enhanced at 1-month follow-up measure. Aim 2. To examine the effects of an 8-week V-RATE intervention on mental health outcomes (i.e., depression, anxiety, posttraumatic stress, cognitive function, health-related quality of life), among women veterans. We hypothesize that after controlling for socio-demographic variables and physical activity history, individuals in the V-RATE group will exhibit more improvement in the mental health indicators after the intervention compared to individuals in the control group. We further hypothesize gains maintained or enhanced at 1-month follow-up measure. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05563805
Study type Interventional
Source The University of Texas at Arlington
Contact Donna L Schuman, PhD
Phone 18172723181
Email donna.schuman@uta.edu
Status Recruiting
Phase N/A
Start date September 7, 2022
Completion date August 31, 2024
View Details
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