Midwife-Led Digital Follow-Up After Cesarean Section
Condition(s) studied
Investigational drug(s) / intervention(s)
Midwife-Led Digital Follow-Up Program: Participants will receive a structured face-to-face education session on the first postpartum day followed by a 4-week digital follow-up program including weekly educational messages, individualized counseling, and continuous support via mobile communication platforms.
Study 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.
Eligibility
Primary outcome measure(s)
- Postpartum Depression — Baseline (first postpartum day), 1 week postpartum, and 4 weeks postpartum
Postpartum depression will be measured using the Edinburgh Postnatal Depression Scale (EPDS), a 10-item self-report scale with total scores ranging from 0 to 30. Higher scores will indicate more severe depressive symptoms. - Perceived Social Support — Baseline (first postpartum day), 1 week postpartum, and 4 weeks postpartum
Perceived social support will be measured using the Multidimensional Scale of Perceived Social Support (MSPSS), a 12-item scale with total scores ranging from 12 to 84. Higher scores will indicate greater perceived social support. - Breastfeeding Self-Efficacy — Baseline, 1 week, and 4 weeks postpartum
Breastfeeding self-efficacy will be measured using the Breastfeeding Self-Efficacy Scale (BSES), a 33-item scale with total scores ranging from 33 to 165. Higher scores will indicate higher breastfeeding self-efficacy.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Giresun University | Giresun | Turkey (Türkiye) | Recruiting |
More Inonu University trials in Turkey
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07523932 on ClinicalTrials.gov ↗ ← All trials in Turkey