Virtual reality offers new hope for chronic arm pain sufferers
NCT ID NCT06523361
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether adding immersive virtual reality (VR) to standard rehab helps people with long-term arm pain (Complex Regional Pain Syndrome) use their arm better. 13 adults took part, using VR during occupational therapy sessions. The goal was to see if VR could improve arm function and reduce pain. Results are still being analyzed.
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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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13 people
The number who actually took part.
- Started
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Nov 2024
- Finished
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Jun 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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 65 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: * Chronic pain in the upper limb, predominantly in one or both upper limbs, for more than 3 months * Age between 18 and 65 * Patient affiliated with or benefiting from a social security organization * Person able to tolerate the virtual reality device * Informed consent form signed Exclusion Criteria: * Upper limb surgery \< 6 months * Infection or pathology of the central nervous system or active cancer * Fibromyalgia * Severe psychiatric or cognitive disorders * Diabetes mellitus complicated by peripheral neuropathy * Neurogenic paraosteoarthropathy or recent fracture * Pregnancy or breast-feeding. * Poor understanding of the French language. * Person deprived of liberty by judicial or administrative decision * Psychiatric disorder * Person subject to a legal protection measure * Person unable to give consent * In connection with the virtual reality device: unstabilized epilepsy, facial trauma \< 3 months, hearing or visual impairment, pain, dizziness or nausea caused by the use of virtual reality.
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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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CH LAVAL
Laval, 53000, France
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CHU Angers
Angers, 49933, France