Clinical Trial

Midwife-Led Digital Follow-Up After Cesarean Section

Study acronym: MID-CS
Not Yet Recruiting
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Summary
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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-04-05.
Trial Details
NCT Number NCT07523932
Lead Sponsor Inonu University
Collaborators: Kahramanmaras Sutcu Imam University
Conditions Postpartum Depression, Breastfeeding, Postpartum Period
Enrollment 104 participants
Start Date 2026-06
Primary Completion 2026-09 (estimated)
Study Completion 2026-10 (estimated)
Updated on ClinicalTrials.gov 2026-04-16