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New program aims to boost breastfeeding confidence after C-Section

NCT ID NCT07474402

Symptom relief Sponsor: Cumhuriyet University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests a multi-component breastfeeding support program for mothers who gave birth by cesarean section. The program includes education, counseling, and follow-ups to help mothers feel more confident about breastfeeding and improve mother-baby bonding. Researchers are recruiting 100 first-time mothers who delivered by C-section and are exclusively breastfeeding.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Multi-Component Breastfeeding Support Program (behavioral intervention: education, psychosocial support, video, message, telephone follow-ups, and individualized counseling)
What this could lead to
If it works, this program could help new mothers feel more confident about breastfeeding and strengthen the bond with their baby after a C-section.
What could go wrong
This is a small, early-stage study with only 100 participants, so results may not apply to all mothers. The program is behavioral, so individual responses may vary.

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

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2026

Expected to finish

Nov 2026

An estimate. End dates often move.

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 years and older

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: \- Primiparous mothers who have completed pregnancy Mothers who delivered by cesarean section (C/S) Mothers in the early postpartum period Mothers aged 18 years and older Mothers who are exclusively breastfeeding Mothers with healthy and stable infants Mothers with no medical conditions that may interfere with breastfeeding Mothers who can read and understand Turkish and complete the data forms Exclusion Criteria: * Mothers who experienced postpartum complications Infants with severe health problems, congenital anomalies, or requiring intensive care Infants hospitalized in neonatal intensive care unit Mothers with medical or psychiatric conditions that prevent breastfeeding Mothers with multiple pregnancies (twins, triplets, etc.) Mothers who cannot attend follow-up visits during the study Mothers without mobile phones Mothers who received breastfeeding education during pregnancy

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As listed by the trial registrant

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

Breastfeeding consultancy training Breastfeeding self-efficacy Mother-infant attachment Primigravida women

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Sivas Cumhuriyet University Hospital

    RECRUITING

    Sivas, Merkez, 58030, Turkey (Türkiye)

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