VR headsets tested as Drug-Free pain relief for End-of-Life care
NCT ID NCT07214090
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether using a virtual reality headset for 10 minutes a day can reduce pain, anxiety, and fatigue in people receiving palliative care. Forty adults with complex needs will be randomly assigned to either a fully immersive VR experience or a control version that keeps them aware of their real surroundings. Researchers will measure changes in pain scores and physiological signals like heart rate and brain activity over one week.
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 (VR) headset
- What this could lead to
- If it works, this could offer a drug-free way to ease pain and anxiety for people in palliative care, improving their comfort and quality of life.
- What could go wrong
- This is a very small pilot study with only 40 people, so results may not apply to everyone. The effect may be small or no better than a placebo.
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.
- Participants
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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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May 2026
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.
Who is studied
Study participants will be recruited from the palliative care unit or through the mobile palliative care team at Strasbourg University Hospitals.
- Ages
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18 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient ≥ 18 years old * Hospitalized in the palliative care unit or followed by the mobile palliative care team of the Strasbourg University Hospitals * Estimated life expectancy \> 1 month (Pronopall score calculated based on medical record data) * Affiliated with a social security scheme * Able to understand the objectives and risks of the trial * Able to understand and complete study questionnaires written in French * Reachable by phone or email for the entire duration of participation in the study Exclusion Criteria: * Patient with a psychotic mental illness, followed and treated before the study, and not stabilized * Patient with a severe neurological disease, followed and treated before the study, and not stabilized * Patient with visual or auditory disorders, or motion sickness, present before the study, that could interfere with the use of virtual reality * Patient under legal protection or unable to express their consent
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Genom att skicka in godkänner du våra Användarvillkor
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 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.
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Other studies related to the condition(s) this trial covers.
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