RECRUITING

Exploring Virtual Reality Adventure Training Exergaming

Conditions

Physical Activity Sedentary Behavior Depression Cognitive Function Post Traumatic Stress Disorder Quality of Life Anxiety

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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 to examine effects on physical and mental health outcomes.

Official Title

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

Quick Facts

Study Start:2022-09-07

Study Completion:2025-08-31

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05563805

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 45 Years

Sexes Eligible for Study:FEMALE

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT

Inclusion Criteria	Exclusion Criteria
1. Are between the ages of 18 and 45 2. Identify as a U.S. military veteran 4. Normal vision (no colorblindness)	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.

Inclusion Criteria

Exclusion Criteria

1. Are between the ages of 18 and 45
2. Identify as a U.S. military veteran
4. Normal vision (no colorblindness)

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.

Contacts and Locations

Study Contact

Donna L Schuman, PhD

CONTACT

18172723181

donna.schuman@uta.edu

Xiangli Gu, PhD

CONTACT

817-818-2106

xiangli.gu@uta.edu

Study Locations (Sites)

University of Texas at Arlington

Arlington, Texas, 76019

United States

Collaborators and Investigators

Sponsor: The University of Texas at Arlington

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-09-07

Study Completion Date2025-08-31

Study Record Updates

Study Start Date2022-09-07

Study Completion Date2025-08-31

Terms related to this study

Additional Relevant MeSH Terms

Physical Activity
Sedentary Behavior
Depression
Cognitive Function
Post Traumatic Stress Disorder
Quality of Life
Anxiety