Can VR games ease phantom limb pain? new study says maybe
NCT ID NCT05296265
First seen Jun 27, 2026 · Last updated Sep 10, 2026 · Updated 2 times
Summary
This study tested two virtual reality (VR) treatments for phantom limb pain in 46 people who had a leg amputated. One group played VR games that made them move their virtual leg, while the other group watched a relaxing VR scene. The goal was to see if either approach could reduce pain intensity and improve pain quality. The study is already completed, and results may help develop drug-free pain relief options.
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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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46 people
The number who actually took part.
- Started
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May 2022
- Finished
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Apr 2025
- 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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18 to 100 years
- 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: 1. Age 18 - 100 years 2. Capacity to provide Informed Consent 3. Unilateral above or below knee amputation more than 3 months prior to enrollment 4. Absence of cognitive impairment, operationally defined as a Montreal Cognitive Assessment score of 18 or greater 5. Pain averaged over the preceding 1 month in the phantom limb rated as greater than 4 on a scale of 0-10. Exclusion Criteria: 1. History of significant medical or neurological disorder such as stroke or moderate to severe traumatic brain injury (operationally defined as loss of consciousness for more than 30 minutes) 2. History of significant or poorly controlled psychiatric disorders 3. Current significant depression or anxiety as judged by the Hospital Anxiety and Depression Scale (HADS) (Zigmond \& Snaith, 1983). 4. Current abuse of alcohol or drugs, prescription or otherwise 5. Nursing a child, pregnant, or intent to become pregnant during the study
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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.
Contacts and locations
Locations
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Moss Rehabilitation Research Institute
Elkins Park, Pennsylvania, 19027, United States
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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
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University of Washington-Harborview Medical Center
Seattle, Washington, 98104, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Spinal Add-On may ease phantom pain after amputation
- Botox shot may silence stubborn nerve pain in amputees
- Battlefield injuries: new study seeks to predict chronic pain before it starts
- Brain implant that turns on only when pain strikes shows promise
- New study seeks to uncover hidden pain in child amputees
- Can VR ease phantom limb pain after amputation?