Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
Healthy Volunteers
NCT07478341

Hybrid Breastfeeding Education in Late Pregnancy: Effects on Antenatal Attachment and Breastfeeding

Led by Emel GÜÇLÜ CİHAN · Updated on 2026-03-17

64

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

Sponsors

E

Emel GÜÇLÜ CİHAN

Lead Sponsor

K

Kahramanmaras Sutcu Imam University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This randomized controlled study aims to examine the effect of individualized hybrid breastfeeding education provided during late pregnancy on antenatal attachment and breastfeeding behaviors among first-time mothers. Participants will be randomly assigned to either the intervention or control group. Women in the intervention group will receive individualized hybrid breastfeeding education beginning at the 36th week of pregnancy. The program includes a face-to-face individual breastfeeding education session at 36 weeks of pregnancy and a reinforcement and practice session at 38 weeks. Participants will also have access to personalized digital educational materials, short educational videos, and online consultation support. In the postpartum period, participants will receive an online support session during the first week after birth and a follow-up session through online communication or telephone at the sixth postpartum week. The control group will receive routine hospital education during pregnancy. After completion of the study, the same educational materials will be provided to the control group in accordance with ethical principles. Data will be collected using the Demographic Information Form, Breastfeeding Behavior Evaluation Form, Antenatal Attachment Inventory, and Breastfeeding Self-Efficacy Scale. Written informed consent will be obtained from all participants prior to enrollment.

CONDITIONS

Official Title

Hybrid Breastfeeding Education in Late Pregnancy: Effects on Antenatal Attachment and Breastfeeding

Who Can Participate

Age: 18Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 to 35 years
  • At 36 weeks of gestation or later
  • Experiencing their first pregnancy (primiparous)
  • Having a singleton pregnancy
  • Able to read and write in Turkish and capable of communication
  • Having access to a smartphone or the internet
  • Free from any physical or mental health problems that would prevent participation in the education
  • Willing to voluntarily participate and provide written informed consent
Not Eligible

You will not qualify if you...

  • Presence of chronic physical illness or pregnancy complications such as preeclampsia or gestational diabetes
  • Multiple pregnancy
  • Gestation earlier than 36 weeks
  • Inability to actively participate due to communication barriers or cognitive impairment
  • Lack of access to a smartphone or the internet
  • Failure to attend any stage of the educational program or voluntary withdrawal
  • Refusal to participate or failure to sign the informed consent form

AI-Screening

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Trial Site Locations

Total: 1 location

1

Elbistan Devlet Hastanesi

Elbistan, Kahramanmaraş, Turkey (Türkiye), 46040

Actively Recruiting

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Research Team

A

Asst. Prof.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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