MedPath

Virtual Reality Gaming for Exercise and Mindfulness Among Pediatric Cancer Rehabilitation

Phase 1
Recruiting
Conditions
Pediatric Cancer
Registration Number
NCT06298357
Lead Sponsor
University of Alabama at Birmingham
Brief Summary

This study will explore the potential benefits of a virtual reality gaming program that focuses on mindfulness and exercise among pediatric cancer rehabilitation patients. The program will last 8 weeks outside of the hospital. Participants will start immediately in the hospital (immediate start group) or wait 8 weeks after hospital discharge to start the program (waitlist control group).

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
16
Inclusion Criteria
  • >7 years of age
  • medical diagnosis of malignancy or non-malignant condition requiring hematopoietic stem cell transplant or a hospital stay that is anticipated to last for at least 2 weeks
  • a caregiver who can assist the child with the study procedures
Exclusion Criteria
  • complete blindness or deafness
  • inability to operate the hand-held controllers
  • susceptible to motion sickness in virtual reality
  • inability to communicate in English

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Physical activityDaily, starting after consent in the hospital (week 0) and ending after the intervention (intervention week 9)

Steps per day measured by a tri-axial accelerometer (Fitbit Flex).

Secondary Outcome Measures
NameTimeMethod
Minutes of gameplayHospital discharge (approximately week 4), Intervention week 4, and Intervention Week 8.

Minutes of gameplay measured by the Meta Quest headset.

Global HealthWeek 0, ~Week 2 (Post-Transplant), ~Week 4 (hospital discharge), Intervention or Wait Period Week 4, Intervention or Wait Period Week 8.

National Institutes of Health (NIH) PROMIS Global Health Short Form 7+2 survey. The scale consists of 7 items that are summarized into a single score of overall health. Participants respond to items without a recall period on how they would rate their overall health, quality of life, and their physical, mental, and social health, using a 5-point Likert scale with varying response categories.

Forced Expiratory Volume in the first second (FEV1)Week 0, ~Week 2 (Post-Transplant), ~Week 4 (hospital discharge), Intervention or Wait Period Week 4, Intervention or Wait Period Week 8.

FEV1 (Liters) by a Spirometer

Trial Locations

Locations (1)

Children's Hospital of Alabama

🇺🇸

Birmingham, Alabama, United States

Children's Hospital of Alabama
🇺🇸Birmingham, Alabama, United States
Byron Lai, PhD
Contact
205-200-1724
byronlai@uab.edu

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