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Completed

NCT Number: NCT05106634

Evaluation of Breastfeeding Success and Self-Efficacy in Mothers Giving Birth Via Vaginal Delivery or Cesarean Section

This cross-sectional observational study was conducted to compare breastfeeding success and breastfeeding self-efficacy levels of mothers who gave birth via vaginal delivery (spontaneous or via epidural analgesia) or cesarean section (under general or spinal anesthesia).

Completed

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Ul

Bursa, 16059, Turkey (Türkiye)

About this study

This study was conducted by including women, who gave birth via VD or CS in the gynecology clinics of a training and research hospital and a city hospital and were in the postpartum period (after 24 hours).

It compared the breastfeeding self-efficacy and breastfeeding success of mothers who gave birth via CS (under spinal anesthesia or general anesthesia) with those of mothers who gave birth via vaginal delivery (under epidural analgesia or via spontaneous vaginal delivery).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • being aged >18 years old;
  • being literate;
  • having a baby of weight between 2500-4000 g, with 5th minute APGAR score of ≥7, and without congenital diseases and sucking and swallowing problems;
  • not having a disease that prevents breastfeeding;
  • having a full-term (37-42 weeks) VD or CS,
  • agreeing to participate in the study

Exclusion criteria

  • a history of psychological or mental health problems
  • any condition in the mother or infant that was a barrier to breastfeeding
  • baby's admission into the neonatal unit
  • baby's separation from the mother for any reason

Treatment and study plan

Primary outcomes

  1. Breastfeeding success observing

    Time frame: Postpartum 24 hours

    assessed using the LATCH Breastfeeding Assessment Tool

  2. Breastfeeding Self-Efficacy

    Time frame: Early postpartum period (after 24 hours)

    assessed using the Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF)

Sponsors and collaborators

Lead sponsor

Aydin Adnan Menderes University

Other

Registry information

Official study title

Evaluation of Breastfeeding Success and Self-Efficacy Using LATCH in Mothers Giving Birth Via Vaginal Delivery or Cesarean Section: Cross-sectional Study

Important dates

Study start
2019
Primary completion
2020
Study completion
2021
First posted
Nov 4, 2021
Registry last updated
Jul 20, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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