Mirror, mirror on the bed: could it ease labor pain?
NCT ID NCT07659249
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether placing a mirror at the foot of the delivery bed helps first-time mothers during the pushing stage of labor. Researchers want to see if seeing the baby's progress reduces pain, increases feelings of support and control, and shortens the pushing phase. Eighty women will be randomly assigned to either use the mirror or receive standard care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- perineal mirror (device)
- What this could lead to
- If it works, this simple mirror could help women feel more in control and supported during childbirth, and may shorten the pushing phase.
- What could go wrong
- This is a small, early-stage study with only 80 participants. The mirror may not make a meaningful difference, and results may not apply to all births.
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
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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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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 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.
- Ages
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19 to 49 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.
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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: * Women aged 19 and over * Women with term pregnancy (38+0 - 41+6) * Women with singleton pregnancy * Women who have had spontaneous vaginal delivery * Primiparous pregnant women * Women who voluntarily agree to participate in the study will be included. Exclusion Criteria: * Women with high-risk pregnancies * Women with multiple pregnancies
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Düzce Atatürk State Hospital
Düzce, Turkey (Türkiye)
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