Purpose

This study will test the acceptability and benefits of a home-based high-intensity virtual reality exercise program for young people with physical disabilities. The program will last 6 weeks. There will be a total of two visits to the laboratory for exercise-related health assessments. The program includes head-mounted displays (Meta Quest) and off-the-shelf games.

Condition

Eligibility

Eligible Ages
Between 13 Years and 25 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • overweight or obese (based on CDC body mass index normative ranges for age and sex) - physically inactive (<150 min/week of moderate exercise) - Gross Motor Function Classification System level (GMFCS) levels I-IV - Physician clearance to participate - Wifi internet access at home

Exclusion Criteria

  • Complete blindness or deafness - GMFCS level V - Unable to communicate in English - Prone to photosensitive seizures - Pregnant (due to radiation from a Dual Energy X-ray Absorptiometry [DXA] scan

Study Design

Phase
Early Phase 1
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Single Group Assignment
Intervention Model Description
Virtual reality high-intensity exercise in either the seated or standing position.
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Virtual Reality Exergaming Intervention
High-intensity active video gaming at the home.
  • Behavioral: Virtual reality exergaming
    High-intensity active video gaming using head-mounted display.

More Details

Status
Active, not recruiting
Sponsor
University of Alabama at Birmingham

Study Contact

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.