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Midwife-Led Digital Follow-Up After Cesarean Section

RecruitingNAAges 18 Years - 45 YearsFemaleInonu University
NCT07523932 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This randomized controlled trial aims to evaluate the effect of a midwife-led digital follow-up program on postpartum depression, perceived social support, and breastfeeding self-efficacy in women who will undergo cesarean section. Participants will be randomly assigned to either an intervention group that will receive structured face-to-face education followed by a 4-week digital follow-up program, or a control group that will receive routine postpartum care. Data will be collected at baseline (postpartum day 1), at 1 week, and at 4 weeks postpartum using validated measurement tools. The study will provide evidence on the effectiveness of continuous, midwife-led digital support in improving maternal psychological well-being and breastfeeding outcomes in the early postpartum period.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Women aged between 18 and 45 years * Women who have undergone cesarean section * Within the first 24 hours postpartum * Able to communicate in Turkish * Having a healthy singleton newborn * Willing to participate and provide informed consent Exclusion Criteria: * History of psychiatric disorders * Presence of severe maternal complications * Newborn requiring intensive care unit admission * Women with communication difficulties * Participation in another intervention study
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What it tests

  • Midwife-Led Digital Follow-Up Program
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Where

1 site
Giresun University
Giresun, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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