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Recruiting NCT07474402

NCT07474402 The Effect of a Multi-Component Breastfeeding Support Program on Breastfeeding Self-Efficacy and Mother-Infant Bonding in Mothers Following Cesarean Section

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Clinical Trial Summary
NCT ID NCT07474402
Status Recruiting
Phase —
Sponsor Cumhuriyet University
Condition Breastfeeding Self-Efficacy
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2026-02-20
Primary Completion 2026-08-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Breastfeeding Support Program

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2026-02-20 with a primary completion date of 2026-08-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study tests a breastfeeding support program for mothers who give birth by cesarean section. The purpose of the study is to see whether the program helps mothers feel more confident about breastfeeding and improves mother-baby bonding.

Eligibility Criteria

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

Contact & Investigator

Central Contact

shabnam Behnam Makouei, Master's Student

✉ shabnambehnam.bm@gmail.com

📞 +90 552 828 5168

Frequently Asked Questions

Who can join the NCT07474402 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Breastfeeding Self-Efficacy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07474402 currently recruiting?

Yes, NCT07474402 is actively recruiting participants. Contact the research team at shabnambehnam.bm@gmail.com for enrollment information.

Where is the NCT07474402 trial being conducted?

This trial is being conducted at Sivas, Turkey (Türkiye).

Who is sponsoring the NCT07474402 clinical trial?

NCT07474402 is sponsored by Cumhuriyet University. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology