Virtual Reality for Pain Management in Burn Patients

ConditionPain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8+
SponsorWeill Medical College of Cornell University

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

Treatment groups

50 Participants
are divided into 2 treatment groups