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Clinical Trials in Turkey / NCT07280000
Starting soon Not applicable

Effect of a Respectful Maternity Care-Based Action Plan in Postpartum Care on Maternal and Neonatal Outcomes

NCT07280000 · tracked via the Priya Life Science Turkey tracker
Sponsor
ilayda sel
Phase
Not applicable
Started
2025-12-10
Last updated
2025-12-12

Condition(s) studied

Postpartum CareMaternal Health CareNewborn HealthPostpartum Depression (PPD)BreastfeedingQuality of CareMaternal Satisfaction

Investigational drug(s) / intervention(s)

Respectful Maternity Care Training and Action Plan

Respectful Maternity Care Training and Action Plan: This intervention involves a structured Respectful Maternity Care (RMC) training program for nurses and midwives, followed by the implementation of an evidence-based RMC action plan during postpartum care. The training includes modules on dignity, privacy, informed consent, effective communication, emotional support, newborn bonding and breastfeeding support, and person-centered postpartum practices. Participants in the intervention arm will receive postpartum care according to the RMC guidelines and structured care forms developed for the study.

Study summary

This study will examine whether a Respectful Maternity Care-based action plan can improve the quality of postpartum care and maternal and newborn outcomes. Nurses and midwives will receive a three-day interactive training about respectful, evidence-based postpartum care. After training, a unit-level action plan will be implemented, including supportive visits, educational materials, and feedback meetings. Women receiving routine postpartum care before the intervention will be compared with women receiving care after implementation. Outcomes will include respectful maternity care experiences, maternal satisfaction, exclusive breastfeeding at 6-8 weeks, maternal mental health, mother-infant bonding, and postpartum complications. The goal of this study is to promote respectful, high-quality postpartum care and improve the health and well-being of mothers and newborns.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
49 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Postpartum women aged 18 years and older * Gave birth at 37-42 gestational weeks (vaginal or cesarean) * Have a single, healthy newborn * No chronic medical conditions * No history of high-risk pregnancy or fetal complications * No communication barriers (e.g., visual or hearing impairment) * Able to speak and understand Turkish * Literate and able to read and write in Turkish Exclusion Criteria: * Development of maternal or neonatal complications during the postpartum follow-up period * Inability to reach the mother at the 8-week postpartum follow-up

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Bakırköy Dr. Sadi Konuk Training and Research Hospital Istanbul Turkey (Türkiye)

Other trials for the same condition

Official registry record

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 NCT07280000 on ClinicalTrials.gov ↗ ← All trials in Turkey