Virtual reality headsets tested to calm C-Section patients
NCT ID NCT06622408
First seen Jun 27, 2026 · Last updated Jul 02, 2026 · Updated 1 time
Summary
This study tests whether using a virtual reality headset during a scheduled cesarean section can help reduce pain and anxiety. Twenty women will be offered the headset at different stages of care, from admission to after birth. Researchers will measure how many accept and use it, and track their pain and anxiety levels.
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 headset (HypnoVR©)
- What this could lead to
- If it works, this could offer a drug-free way to ease pain and anxiety during cesarean sections.
- What could go wrong
- This is a very small feasibility study with only 20 participants, so results may not apply widely. Virtual reality may not reduce pain or anxiety significantly.
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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20 people
The number who actually took part.
- Started
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Nov 2024
- Finished
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Jun 2026
- Lead sponsor
-
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 45 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Major woman ; * Female volunteer ; * Social security affiliation; * Admitted for scheduled caesarean section with history of caesarean section and patient's refusal to attempt vaginal delivery; * Informed patients who have signed the informed consent form. Exclusion Criteria: * Speaks a language other than French; * Unbalanced epilepsy; * People unable to understand (language barrier, cognitive difficulties, cerebral palsy, etc.) and/or apply dietary advice (people institutionalized in nursing homes, retirement homes, prisons, etc.); * Women claiming to have had a very bad experience during their previous caesarean section.
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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
-
CHU Nice - Hôpital de l'Archet 2
Nice, Alpes-Maritimes, 06200, France
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