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Clinical Trials/NCT06723613
NCT06723613
Completed
Not Applicable

Effect of Exercise Program to Increase Breast Milk on Breastfeeding Self-efficacy, Breastfeeding Success and Breast Milk Quantity: A Randomized Controlled Trial

Selcuk University1 site in 1 country122 target enrollmentJanuary 1, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Maternal Behavior
Sponsor
Selcuk University
Enrollment
122
Locations
1
Primary Endpoint
Comparison of mothers' sociodemographic characteristics with survey before intervention
Status
Completed
Last Updated
last year

Overview

Brief Summary

In this study, the effects of an exercise program aimed at increasing breast milk on breastfeeding self-efficacy, breastfeeding success, and breast milk quantity will be evaluated.

Detailed Description

The research is a randomized controlled trial. The research will be conducted with 122 mothers who are in their 8th week postpartum and have healthy babies. Mothers in the exercise group will be given 1 hour (60 minutes) of exercise to increase breast milk three times a week for 6 weeks. The control group will be given routine breastfeeding education. Data will be collected using a sociodemographic form, Breastfeeding Self-Efficacy Scale-Short Form (BSES-SF), LATCH- Breastfeeding Charting system, IMDAT: a tool for assessing the level of maternal milk intake scale.

Registry
clinicaltrials.gov
Start Date
January 1, 2025
End Date
March 1, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Seyhan Çankaya

Principal Investigator Seyhan Çankaya

Selcuk University

Eligibility Criteria

Inclusion Criteria

  • Those who are over 18 years old,
  • Who gave birth at term pregnancy (38-42 weeks),
  • Who have a healthy baby,
  • Who are between 8 weeks postpartum.

Exclusion Criteria

  • Those with diagnosed mental illness (e.g., antidepressants, antianxiety or antipsychotic medications),
  • Those with chronic systemic illnesses,
  • Those with physical illnesses that may prevent them from exercising,
  • Those with any postpartum complications (hemorrhage, postpartum infection, mastitis, thromboembolic disease or postpartum psychiatric disorder).

Outcomes

Primary Outcomes

Comparison of mothers' sociodemographic characteristics with survey before intervention

Time Frame: 3 months

Mothers' sociodemographic characteristics will be collected through surveys and compared and reported

Comparison of mothers' Breastfeeding Self-Efficacy Scale averages by groups

Time Frame: 3 months

Breastfeeding Self-Efficacy Scale will be applied to mothers. Breastfeeding Self-Efficacy Scale is 14-70 points (min-max) and as the score increases, it shows that mothers' breastfeeding self-sufficiency increases.

Comparison of mothers' LATCH- Breastfeeding Charting system averages by groups

Time Frame: 3 months

LATCH- Breastfeeding Charting system will be applied to mothers. LATCH- Breastfeeding Charting system is 0-10 points (min-max) and as the score increases, it shows that the mothers' LATCH score increases.

Comparison of mothers' IMDAT: a tool for assessing the level of maternal milk intake averages by group.

Time Frame: 3 months

IMDAT will be applied to mothers. IMDAT is 0-10 points (min-max) and the higher the score, the better the intake of breast milk.

Study Sites (1)

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