Virtual reality exercise program for women veterans
Exploring Virtual Reality Adventure Training Exergaming (V-RATE) on Veterans' Health Outcomes
This study is testing a new virtual reality exercise program to see if it can help women veterans improve their physical and mental health over eight weeks.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | Female |
| Sponsor | The University of Texas at Arlington Academic / other |
| Locations | 1 site (Arlington, Texas) |
| Trial ID | NCT05563805 on ClinicalTrials.gov |
What this trial studies
This project implements an 8-week Virtual Reality Adventure Therapy Exergaming (V-RATE) intervention aimed at improving physical and mental health outcomes among women veterans. The study employs a randomized controlled trial design with repeated measures and a follow-up assessment one month after the intervention. It focuses on evaluating changes in physical health indicators such as BMI and physical activity, as well as mental health outcomes including depression, anxiety, and cognitive function. The goal is to determine the effectiveness of this innovative approach in enhancing the well-being of participants.
Who should consider this trial
Good fit: Ideal candidates for this study are U.S. military veterans aged 18 to 45 with normal vision.
Not a fit: Patients who are unable to walk independently or have significant mobility issues will not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the physical and mental health of women veterans.
How similar studies have performed: Other studies have shown promising results with virtual reality interventions for physical and mental health, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Are between the ages of 18 and 45 2. Identify as a U.S. military veteran 4\. Normal vision (no colorblindness) Exclusion Criteria: 1. Unable to walk independently (e.g., use of any mobility assistive device such as brace, wheelchair, cane, crutch, walker, knee scooter) 2. Self-reported joint problem that limits mobility (e.g., arthritis or other condition that would prevent participation) or ongoing orthopedic injury 3. Self-reported pregnancy or suspicion of pregnancy 4. Self-reported motor disorder or impaired sense of motion or balance (such as Parkinsonism) 5. Self-reported color blindness 6. Self-reported neurological or cognitive disorder (e.g., TBI, history of seizure) 7. Self-reported cardiac surgery or any ongoing cardiovascular issues preventing participation or physical activity.
Where this trial is running
Arlington, Texas
- University of Texas at Arlington — Arlington, Texas, United States (Recruiting)
Study contacts
- Study coordinator: Donna L Schuman, PhD
- Email: donna.schuman@uta.edu
- Phone: 18172723181
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.