Cuddle at first sight: can Skin-to-Skin contact improve birth and bonding?
NCT ID NCT07656207
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will test whether placing a newborn directly on the mother's chest immediately after birth (before cutting the cord) for about an hour can improve birth outcomes and early parenting behavior. Researchers will track 96 first-time mothers who have a vaginal delivery at full term. They will measure things like pain, breastfeeding motivation, and how parents interact with their baby. The goal is to see if this simple, low-cost practice makes a meaningful difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- immediate skin-to-skin contact after birth
- What this could lead to
- If successful, this could show that simple skin-to-skin contact improves breastfeeding, reduces pain, and strengthens early parenting bonds.
- What could go wrong
- This is a small, early-stage study with only 96 participants, so results may not apply to all mothers. It measures short-term outcomes, not long-term benefits.
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 96 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 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: * Vaginal delivery * Primiparous pregnancy * Delivery at 37 weeks or later * Single, live fetus * Not a high-risk pregnancy * Not an individual with special needs * Able to communicate Exclusion Criteria: * Women who Have a multiple pregnancy, * Develop complications requiring emergency intervention in the mother or baby after delivery, * Have their baby admitted to the neonatal intensive care unit after delivery, * Have a cesarean section, * Withdraw from the study will be excluded from the research.
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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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Tarsus University
Toroslar, Mersin, 33000, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- C-Section babies get skin time: study tests stress and bonding
- New online tool aims to ease Family-Building decisions for young cancer survivors
- Mind over matter: meditation may ease childbirth pain and fear