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Tests treatment safety and results for Breastfeeding Self-Efficacy
Official title The Effect of a Multi-Component Breastfeeding Support Program on Breastfeeding Self-Efficacy and Mother-Infant Bonding in Mothers Following Cesarean Section
ClinicalTrials.gov ID: NCT07474402
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, women only. Healthy volunteers may be eligible.
You may be able to join if
- \- 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
You likely can't join if
- 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
See the full eligibility 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
- 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
The study team makes the final eligibility decision.
Where it's taking place
- Sivas, Merkez, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Sivas, Merkez, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.