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Clinical Trials/NCT06341140
NCT06341140
Completed
Not Applicable

Does Individualized Breastfeeding Support Make a Difference in Exclusive Breastfeeding, Breast Problem Occurrence, and Breastfeeding Self-Efficacy in the First 6 Months: Randomized Controlled Study

Celal Bayar University1 site in 1 country102 target enrollmentAugust 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breastfeeding
Sponsor
Celal Bayar University
Enrollment
102
Locations
1
Primary Endpoint
Situation of mothers feeding their babies exclusively with breast milk
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of the study is to determine the effect of individual breastfeeding support on the lactation process. The research is a randomized controlled experimental study. The sample of the study consisted of pregnant women who applied to the Obstetrics Polyclinic of a university hospital (intervention=51, control=51). In the study, individual breastfeeding education was given to the intervention group during the antenatal period, and a training booklet was given to the control group. In the postpartum period, home visits and phone follow-ups were carried out for both groups between the fifth day and the sixth month. The effect of breastfeeding counseling on the lactation process; The duration of exclusive breastfeeding, breast problems and breastfeeding success was evaluated with. The data of the study were collected using the Pregnant, Postpartum-Newborn Information Form, Breastfeeding Questionnaire, Breast Problems Diagnosis Form, LATCH Breastfeeding Diagnostic Tool and Breastfeeding Self-Efficacy Scale.

Registry
clinicaltrials.gov
Start Date
August 1, 2021
End Date
February 6, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Seçil Köken Durgun

Principal Investigator

Celal Bayar University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • At the beginning of the research;
  • Under 18 years of age,
  • Having a risky pregnancy,
  • Having breastfeeding experience,
  • Less than the 35th gestational week,
  • Residing outside Manisa Central districts (Yunusemre and Şehzadeler),
  • Any maternal disability that may affect breastfeeding,
  • Pregnant women who did not want to participate in the study were excluded.
  • During the research process;
  • Those who want to leave the job,

Outcomes

Primary Outcomes

Situation of mothers feeding their babies exclusively with breast milk

Time Frame: 6 months

Determination of mothers' status of exclusively breastfeeding their babies for the first 6 months using a survey form created by researchers.

Determination of mothers' breastfeeding self-efficacy

Time Frame: 6 months

Breastfeeding competencies were assessed with the LATCH breastfeeding diagnostic tool and the breastfeeding self-efficacy scale. Mothers' breastfeeding success was examined with the LATCH breastfeeding diagnostic tool. On this scale, they can get a minimum of 0 and a maximum of 10 points. As the score increases, breastfeeding success increases. The breastfeeding self-efficacy scale determines the self-efficacy of mothers and can get a minimum of 33 and a maximum of 165 points. As the average score increases, breastfeeding self-efficacy is expressed as high.

Mothers experiencing breast problems

Time Frame: 6 months

Determination of breast problems that occur during the breastfeeding process with a survey created by researchers.

Study Sites (1)

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