Teach-Back Breastfeeding Education After Birth
Effect of Teach-Back Breastfeeding Education on Breastfeeding Success, Breastfeeding Self-Efficacy, and Mother-Infant Bonding in Primiparous Postpartum Women: A Randomized Controlled Trial
1 other identifier
interventional
102
1 country
1
Brief Summary
This study evaluated whether breastfeeding education delivered using the teach-back method improves breastfeeding outcomes and mother-infant bonding among primiparous postpartum women. Early postpartum breastfeeding education is routinely provided in many hospitals; however, women may have difficulty remembering or applying the information after birth. Teach-back is a communication method where the patient is asked to explain the information back in their own words, allowing the educator to check understanding and clarify misconceptions. In this randomized controlled trial, postpartum women who gave birth in a private hospital were assigned either to a teach-back breastfeeding education group or to a control group receiving standard breastfeeding education. Breastfeeding success, breastfeeding self-efficacy, and mother-infant bonding were assessed using validated measurement tools at postpartum 6 hours and again at postpartum 24 hours. The findings of this study aim to support evidence-based postpartum breastfeeding education practices and improve early breastfeeding outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 31, 2024
CompletedFirst Submitted
Initial submission to the registry
February 6, 2026
CompletedFirst Posted
Study publicly available on registry
February 12, 2026
CompletedFebruary 12, 2026
February 1, 2026
4 months
February 6, 2026
February 6, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Breastfeeding Success
Breastfeeding success assessed using the LATCH Breastfeeding Assessment Tool.
At postpartum 6 hours and postpartum 24 hours
Secondary Outcomes (2)
Breastfeeding Self-Efficacy
At postpartum 6 hours and postpartum 24 hours
Mother-Infant Bonding
At postpartum 6 hours and postpartum 24 hours
Study Arms (2)
Teach-Back Breastfeeding Education
EXPERIMENTALParticipants received standard postpartum breastfeeding education plus an additional teach-back session delivered one time at postpartum 3-4 hours. The session lasted approximately 30 minutes in total, including education and participant feedback. Content included key elements of effective breastfeeding (latch, audible swallowing, nipple type, breast/nipple comfort, and positioning/hold) and signs of successful breastfeeding.
Control: Standard Breastfeeding Education
NO INTERVENTIONParticipants received standard postpartum breastfeeding education routinely provided by the hospital (lactation nurse-led), without a teach-back component.
Interventions
Participants received standard postpartum breastfeeding education plus an additional teach-back session delivered one time at postpartum 3-4 hours. The session lasted approximately 30 minutes in total, including education and participant feedback. Content included key elements of effective breastfeeding (latch, audible swallowing, nipple type, breast/nipple comfort, and positioning/hold) and signs of successful breastfeeding.
Eligibility Criteria
You may qualify if:
- Women who gave birth at the study hospital during the study period
- Primiparous postpartum women
- Live birth
- Volunteered to participate and provided informed consent
You may not qualify if:
- Multiparous women
- Neonatal or perinatal loss
- Mothers who refused breastfeeding
- Inability to communicate in Turkish
- Hearing impairment or mental health conditions limiting participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Nilgun Avcilead
Study Sites (1)
State Obstetrics and Gynecology Hospital, Istanbul
Bayrampaşa, Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- phD
Study Record Dates
First Submitted
February 6, 2026
First Posted
February 12, 2026
Study Start
October 1, 2023
Primary Completion
January 31, 2024
Study Completion
January 31, 2024
Last Updated
February 12, 2026
Record last verified: 2026-02