Recruiting

Midwife-Led Digital Follow-Up After Cesarean Section

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…

ClinicalTrials.gov IDNCT07523932
PhaseNA
Enrollment104
SponsorInonu University
Age18 Years
SexFEMALE
I'm interested View official listing

Conditions studied

Postpartum Depression, Breastfeeding, Postpartum Period

About this study

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.

Interventions

Primary outcomes

Eligibility information

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

Study locations

Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.

Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.