The Effect of a Multi-Component Breastfeeding Support Program on Breastfeeding Self-Efficacy and … (NCT07474402) | Clinical Trial Compass
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The Effect of a Multi-Component Breastfeeding Support Program on Breastfeeding Self-Efficacy and Mother-Infant Bonding in Mothers Following Cesarean Section
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.
Who can participate
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.