Could a VR headset replace painkillers during labor induction?
NCT ID NCT05155826
First seen Jun 30, 2026 · Last updated Jul 01, 2026 · Updated 1 time
Summary
This study tests whether using a virtual reality headset during placement of a cervical ripening balloon can reduce pain and anxiety for women undergoing labor induction. Sixty pregnant women will either receive standard care or standard care plus a VR experience. The goal is to see if distraction through VR lowers the maximum pain felt during the procedure.
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 (Deepsen® VRx)
- What this could lead to
- If effective, virtual reality could offer a drug-free way to manage pain and anxiety during labor induction procedures.
- What could go wrong
- This is a small, early-stage trial with only 60 participants, so results may not apply widely. The effect may be limited to distraction and not reduce actual pain.
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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60 people
The number who actually took part.
- Started
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Feb 2022
- Finished
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Feb 2023
- 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 years and older
- Sex
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Female 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.
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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: * Any pregnant woman presenting to the Gynecology-Obstetrics Department of the Saint-Etienne University Hospital for an induction by Cook's balloon. * Patients affiliated or entitled to a social security system * Patients having given their agreement to participate and after signing the consent form Exclusion Criteria: * Woman refusing to participate in the study (lack of consent) * Non French-speaking woman (impossibility of carrying out a good quality interview of the pregnant woman) * Women suffering from blindness, deafness or epilepsy against the use of the virtual reality helmet. * Participation in another interventional study. * Patient under guardianship or curatorship * Patient subject to a legal protection measure or unable to express their consent
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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 de Saint-Etienne
Saint-Etienne, 42055, France
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Other studies related to the condition(s) this trial covers.
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