NCT07407335

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
102

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2024

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

February 6, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 12, 2026

Completed
Last Updated

February 12, 2026

Status Verified

February 1, 2026

Enrollment Period

4 months

First QC Date

February 6, 2026

Last Update Submit

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

EXPERIMENTAL

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.

Behavioral: Teach-Back Breastfeeding Education

Control: Standard Breastfeeding Education

NO INTERVENTION

Participants 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.

Teach-Back Breastfeeding Education

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

State Obstetrics and Gynecology Hospital, Istanbul

Bayrampaşa, Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Breast Feeding

Condition Hierarchy (Ancestors)

Feeding BehaviorBehavior

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

Locations