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The Effect of Postpartum Breastfeeding Education on Breastfeeding Self-efficacy and Breastfeeding Success

NCT05666817 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2022-12-28

No results posted yet for this study

Summary

Objective: This study will be conducted as a pre-test post-test randomized controlled study in order to determine the effect of postpartum breastfeeding education given to women who had normal vaginal delivery and cesarean section on breastfeeding self-efficacy and breastfeeding success.

Materials and Methods: The data of the study were collected with "Descriptive Information Form, Breastfeeding Knowledge Level Diagnosis Form, LATCH Breastfeeding Diagnosis and Evaluation Scale and Postpartum Breastfeeding Self-Efficacy Scale". SPSS 25.0 (Statistical Package for Social Science) program will be used in the analysis of the data.

Design: Randomized controlled.

The study included 76 women who had normal vaginal and cesarean delivery and met the inclusion criteria (Research Research group, 38 control group) in Zeynep Kamil Gynecology and Pediatrics Education and Hospital Postpartum Postpartum Postpartum Service in Istanbul.

Conditions

  • Breastfeeding

Interventions

OTHER

breastfeeding education

Mothers in the intervention group will be given breastfeeding training after the pre-test application. The content of breastfeeding education is as follows; * General information about breastfeeding, * General information about breast milk and the benefits of breast milk, * Benefits of breastfeeding for mother and baby, * How the baby should be held during breastfeeding, the baby's position, * Effective breastfeeding positions for the mother, * Ensuring that the baby holds the breast correctly, * Providing the correct breastfeeding technique, * Breast milking and storage conditions, * The necessity and benefits of continuing breastfeeding.

Sponsors & Collaborators

  • Saglik Bilimleri Universitesi

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-12-10
Primary Completion
2022-12-18
Completion
2022-12-18

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05666817 on ClinicalTrials.gov