Actively Recruiting
iMOVE: Virtual Reality PT Versus Traditional PT
Led by Stanford University · Updated on 2025-11-18
40
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This pragmatic, crossover, randomized controlled study evaluates the efficacy of virtual reality assisted physical therapy (VRPT) for improving the physical activity of hospitalized children as compared to traditional physical therapy. This is a pilot study that will be used to identify patient populations that can benefit the most from VRPT and estimate this effect for future studies. Patients with a significant neurological condition, major developmental disability, active infection of the face or hand, history of severe motion sickness, history of seizures caused by flashing light or had a major surgery within the last 48 hours will be excluded.
CONDITIONS
Official Title
iMOVE: Virtual Reality PT Versus Traditional PT
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between age 10-25 years
- Diagnosed with cancer
- Has an active physical therapy consultation
- Anticipated inpatient stay for at least 3-days with the second physical therapy session between 24-72 hours after the first
- Ability and willingness to sign informed consent or assent documents as appropriate
You will not qualify if you...
- Legal guardian does not present to obtain consent
- Significant neurological condition or major developmental disability
- Active infection of the face or hand
- History of severe motion sickness
- History of seizures caused by flashing light
- Major surgery within the last 48 hours
- Does not speak English (required for surveys)
- Visual impairments or any degree of developmental delays
- On mechanical ventilation or ventilatory support
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Lucile Packard Childrens Hospital Stanford
Palo Alto, California, United States, 94304
Actively Recruiting
Research Team
T
Thomas Caruso
CONTACT
M
Man Yee Suen
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here