Actively Recruiting
The Effect of a Multi-Component Breastfeeding Support Program on Breastfeeding Self-Efficacy and Mother-Infant Bonding in Mothers Following Cesarean Section
Led by Cumhuriyet University · Updated on 2026-03-25
100
Participants Needed
1
Research Sites
40 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
The Effect of a Multi-Component Breastfeeding Support Program on Breastfeeding Self-Efficacy and Mother-Infant Bonding in Mothers Following Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sivas Cumhuriyet University Hospital
Sivas, Merkez, Turkey (Türkiye), 58030
Actively Recruiting
Research Team
S
shabnam Behnam Makouei, Master's Student
CONTACT
P
Prof. Dr. Nilüfer Tuğut, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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