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Clinical Trials/NCT05106634
NCT05106634
Completed
Not Applicable

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

Aydin Adnan Menderes University1 site in 1 country106 target enrollmentSeptember 10, 2019
ConditionsBreastfeeding

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breastfeeding
Sponsor
Aydin Adnan Menderes University
Enrollment
106
Locations
1
Primary Endpoint
Breastfeeding success observing
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

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).

Detailed Description

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).

Registry
clinicaltrials.gov
Start Date
September 10, 2019
End Date
October 22, 2021
Last Updated
2 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Aydin Adnan Menderes University
Responsible Party
Principal Investigator
Principal Investigator

Gonca Buran

RN, PhD, lecturer

Uludag University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Breastfeeding success observing

Time Frame: Postpartum 24 hours

assessed using the LATCH Breastfeeding Assessment Tool

Breastfeeding Self-Efficacy

Time Frame: Early postpartum period (after 24 hours)

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

Study Sites (1)

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