VR for Surgical Prehabilitation and Rehabilitation
- Conditions
- FrailtySurgeryBreast Cancer
- Registration Number
- NCT06334380
- Lead Sponsor
- Stanford University
- Brief Summary
This randomized controlled trial aims to determine feasibility and acceptability of of VR-physical therapy modules for surgical patients undergoing breast or axilla surgery in order to prepare for and recover from surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ENROLLING_BY_INVITATION
- Sex
- All
- Target Recruitment
- 30
- 18+ years of age
- English speaking
- Will undergo breast or axilla surgery at Stanford
- Have access to internet and stable Wifi at home
- Have access to a space with stable chair at home
- Ability to sit-to-stand without significant balance issues
- Absence of chronic vertigo or nausea/vomiting
- Agreeable to up to 4 weeks of prehab prior to surgery and up to 8 weeks of post-operative rehab
- Inability to engage in PT due to physical limitations identified by the participant and/or care team
- Inability to complete a brief online survey at three time points during the duration of the study
- Inability to consent
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method VR for remote Physical Therapy (PT) 12 weeks This study will evaluate the feasibility of using VR technology to perform PT remotely from patients' homes to prepare for and recover from surgery. Frequency of engagement with the VR system (e.g., number of times participant initiated a VR physical therapy module, how long each session was used for) will be measured. Engagement with the live PT sessions will be measured.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Stanford Hospital and Clinics
🇺🇸Palo Alto, California, United States
Stanford Hospital and Clinics🇺🇸Palo Alto, California, United States