A mirror in the delivery room: could it reduce Post-Birth pain and lift mood?
NCT ID NCT07792629
First seen Aug 28, 2026 · Last updated Sep 02, 2026 · Updated 2 times
Summary
This trial tests whether mirror therapy, where a woman watches her own body and the birth process in a mirror during labor, can improve her experience. Researchers will compare postpartum pain, mood, and emotional well-being in women who use the mirror versus those who do not. The goal is to see if this simple, drug-free approach helps women feel more in control and recover better after childbirth.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Mirror therapy, a non-drug approach where a woman watches her own body and the birth process in a mirror during labor
- What this could lead to
- If it works, mirror therapy could become a simple, drug-free tool to help women feel more in control during childbirth and recover with less pain and better mood.
- What could go wrong
- This is a small, early-stage trial, so the benefits may not hold up in larger groups. Mirror therapy may also not suit every birth, especially if complications arise.
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 86 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2026
- Expected to finish
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Feb 2027
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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18 years and older
- 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: * Women aged 18 years or older, * Able to read and write in Turkish, * Admitted for vaginal delivery, * Willing to participate voluntarily in the study, * Providing written informed consent by signing the "Informed Voluntary Consent Form." Exclusion Criteria: * Having difficulty communicating, * Having a high-risk pregnancy (e.g., hypertension, diabetes), * Experiencing complications during labor or delivery (e.g., emergency cesarean section, fetal distress).
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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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Ağrı İbrahim Çeçen University
RECRUITINGAğrı, Ağri, 04100, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Ultrasound before induced labor may reveal delivery risks
- Mind over matter: could breathing and focus during labor shield pelvic floor?
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- Simple strength tests and surveys may predict labor complications
- Simple drug may prevent worrisome fetal heart tracings after epidural