About this trial
This study is a randomized proof-of-concept study to assess the efficacy of Virtual Reality (VR) vs standard of care in 50 adult patients in the New York Presbyterian Burn Unit. The participants who are randomized to receive the virtual reality intervention will also receive opioids, which is the standard of care and is known to be effective. Participants will be randomly assigned to two groups. The first group will receive VR during their painful procedure (e.g., wound dressing changes, physical therapy etc.) in addition to the standard of care. The other group will receive standard of care (and no VR).
Eligibility criteria
Qualifiers
8 years and older
Patients with a burn injury and is in the Burn Unit at New York Presbyterian
Awake, alert, ambulatory
The burn comprises less than 15% total body surface area (TBSA)
Disqualifiers
Diagnosis of a cognitive disorder, psychotic disorder or bipolar I as determined by self-report from previous diagnosis
Current opioid abuse
Trial design
Treatments tested in this trial
- Virtual Reality