Virtual reality tested as pain relief for burn patients
NCT ID NCT04685486
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests whether playing an immersive virtual reality game during painful burn treatments (like dressing changes) can reduce pain and the need for opioid painkillers. Fifty adult burn patients will be randomly assigned to receive either standard care alone or standard care plus VR. The goal is to see if VR can make procedures less painful and lower medication doses.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Virtual reality (immersive game via head-mounted display)
- What this could lead to
- If it works, this could offer a drug-free way to ease pain during burn treatments, potentially reducing reliance on opioids.
- What could go wrong
- This is a small, early proof-of-concept study. The effect may be small or not last beyond the procedure, and VR may not work for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2018
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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8 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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) * The patient does not require conscious sedation such as ketamine for staple removal or wound dressing changes * The patient is able to give informed consent Exclusion Criteria: * Diagnosis of a cognitive disorder, psychotic disorder or bipolar I as determined by self-report from previous diagnosis * Current opioid abuse
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Weill Cornell Medicine
RECRUITINGNew York, New York, 10065, United States
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