Actively Recruiting
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
Eligibility Criteria
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
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
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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