Can a VR headset calm chemo anxiety? new study tests hypnosis in prostate cancer patients
NCT ID NCT04533958
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether using virtual reality hypnosis before chemotherapy infusions could lower anxiety in men with metastatic prostate cancer. Fifty-three patients were randomly assigned to either receive the VR hypnosis session or standard care before each docetaxel infusion. Researchers measured anxiety levels and nausea to see if the VR approach made treatment less stressful.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- HYPNO VR® device (virtual reality hypnosis software with headset and headphones)
- What this could lead to
- If it works, this could offer a drug-free way to reduce anxiety and nausea during chemotherapy for men with metastatic prostate cancer.
- What could go wrong
- This is a small, single-center study with only 53 participants, so results may not apply to everyone. The effect on anxiety may be modest or no different from standard care.
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
-
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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53 people
The number who actually took part.
- Started
-
Sep 2020
- Finished
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Feb 2026
- 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
-
18 years and older
- Sex
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Male participants only
- 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: * Man aged ≥ 18 years * Histologically proven metastatic prostate adenocarcinoma, * Patient undergoing chemotherapy according to the following conventional scheme: 12 courses of Docetaxel every two weeks * Patient who signed their informed consent * Patient benefiting from social security coverage * Patient treated and followed in the center for the duration of the study (6 months maximum). Exclusion Criteria: * Patient participating in another clinical trial on an experimental molecule * Patient who received previous chemotherapy * Patient unable to submit to protocol monitoring for psychological, social, family or geographic reasons * Patient deprived of their liberty or under guardianship * Patient with underlying or concomitant pathology incompatible with inclusion in the trial, whether psychiatric or somatic
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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
-
CHP Saint-Grégoire
Saint-Grégoire, 35760, France
-
Clinique Pasteur-Lanroze
Brest, 29200, France
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Clinique de la Côte d'Emeraude
St-Malo, 35400, France
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Hospital Lusiadas Amadora
Amadora, 2724-002, Portugal
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Hospital Lusiadas Lisboa
Lisbon, 1500-458, Portugal
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Hospital Lusiadas Porto
Porto, 4050-115, Portugal
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Other studies related to the condition(s) this trial covers.
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