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C-Section babies get skin time: study tests stress and bonding

NCT ID NCT07111949

Knowledge-focused Sponsor: Kutahya Health Sciences University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 2 times

Summary

This study looks at whether placing a newborn directly on the mother's chest right after a C-section (instead of waiting) can lower stress for both. Researchers will measure baby stress levels, breastfeeding success, and mother pain and stress. About 120 mothers having planned C-sections will take part.

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

100 people

The number who actually took part.

Started

Mar 2025

Finished

Oct 2025

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

18 to 45 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show 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: Mothers; * Planning a cesarean section with spinal anesthesia * Being between the ages of 18-45 * Having a singleton pregnancy * Being between the gestational age of 37-40 weeks * Not having any known health problems (diabetes, gestational diabetes, hypertension, preeclampsia, renal failure, cardiac problems, psychiatric disorders, etc.) * Agreeing to participate in the study * Having stable general conditions and vital signs before the skin-to-skin contact procedure * Residing in Kütahya Newborns (0-28 days) * Having a gestational age between 37-40 weeks * Having a birth weight between 2500-4500 grams * 1-5. Apgar score ≥ 7 per minute * No health problems, anomalies or congenital diseases * No conditions that prevent sucking such as frenulum (tongue tie) or palate problems Exclusion Criteria: * Caesarean births performed with general anesthesia * Normal births

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Conditions

The condition(s) this trial relates to.

Pain

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Skin to skin contact

Contacts and locations

Locations

  • Kütahya Health Sciences University

    Merkez, Kütahya, 43100, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.