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Clinical Trials/NCT07407335
NCT07407335CompletedNot Applicable

Effect of Teach-Back Breastfeeding Education on Breastfeeding Success, Breastfeeding Self-Efficacy, and Mother-Infant Bonding in Primiparous Postpartum Women: A Randomized Controlled Trial

Nilgun Avci1 site in 1 country102 target enrollmentStarted: October 1, 2023Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
102
Locations
1
Primary Endpoint
Breastfeeding Success

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Women who gave birth at the study hospital during the study period
  • Primiparous postpartum women
  • Live birth
  • Volunteered to participate and provided informed consent

Exclusion Criteria

  • Multiparous women
  • Neonatal or perinatal loss
  • Mothers who refused breastfeeding
  • Inability to communicate in Turkish
  • Hearing impairment or mental health conditions limiting participation

Arms & Interventions

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.

Intervention: Teach-Back Breastfeeding Education (Behavioral)

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.

Outcomes

Primary Outcomes

Breastfeeding Success

Time Frame: At postpartum 6 hours and postpartum 24 hours

Breastfeeding success assessed using the LATCH Breastfeeding Assessment Tool.

Secondary Outcomes

  • Breastfeeding Self-Efficacy(At postpartum 6 hours and postpartum 24 hours)
  • Mother-Infant Bonding(At postpartum 6 hours and postpartum 24 hours)

Investigators

Sponsor
Nilgun Avci
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Nilgun Avci

phD

Biruni University

Study Sites (1)

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