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…
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
- Behavioral: 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.
Primary outcomes
- Postpartum Depression (Baseline (first postpartum day), 1 week postpartum, and 4 weeks postpartum)
- Perceived Social Support (Baseline (first postpartum day), 1 week postpartum, and 4 weeks postpartum)
- Breastfeeding Self-Efficacy (Baseline, 1 week, and 4 weeks postpartum)
Eligibility information
Study locations
- Giresun University, Giresun, 28200 Turkey (Türkiye)
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.