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Clinical Trials in Turkey / NCT07295639
Starting soon Not applicable

Mobile Prenatal Education for Expectant Fathers and Its Effects on Bonding, Stress, Breastfeeding and Marital Satisfaction

NCT07295639 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01
Last updated
2025-12-19

Condition(s) studied

Breastfeeding AttitudesBreast FeedingPaternal BehaviorHealth EducationParent-Child Relations

Investigational drug(s) / intervention(s)

Mobile-based application

Mobile-based application: The intervention is a six-module mobile-based training programme developed specifically for expectant fathers. The modules cover baby care, nutrition, sleep patterns, health and safety, emotional development and daily care. The aim is to strengthen the father-baby bond, reduce stress levels and develop a positive attitude towards breastfeeding.

Study summary

The aim of this interventional clinical trial is to assess whether a mobile-based antenatal education programme for expectant fathers has a positive effect on father-infant bonding, stress levels, and breastfeeding attitudes.

The study aims to answer the following main questions:

Does participation in a mobile-based prenatal education programme strengthen fathers' emotional bonds with their babies? Does the education reduce fathers' stress levels during the prenatal and postnatal periods? Does it increase the father's knowledge and supportive attitude towards breastfeeding? Researchers will compare whether there are measurable differences in attachment, stress, and breastfeeding attitudes between the intervention group (fathers receiving mobile-based education) and the control group (fathers receiving standard routine information).

Participants: Will complete pre- and post-intervention questionnaires assessing attachment, stress, and breastfeeding attitudes.

The intervention group will have access to a six-module mobile application covering topics such as infant care, nutrition, sleep routines, health and safety, emotional development, and daily care practices.

The study will be conducted with fathers aged 19-65 who became fathers within the last month and voluntarily agreed to participate.

Eligibility

Sex
MALE
Min age
19 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age between 19 and 65 years * First-time father * Has become a father within the last month * Has a healthy newborn without congenital anomalies or chronic illnesses * Does not have a premature or low-birth-weight baby * Has not become a father through adoption * Owns a mobile phone capable of accessing the mobile-based application * Has an Android or iOS operating system * Has not received any infant care training within the last 6 months * Has no physical or mental disability that would prevent viewing, hearing, or understanding the research questions or educational content * Voluntarily agrees to participate in the research Exclusion Criteria: * Declines to participate in the research * Does not own a smartphone * Cannot use mobile applications * Has a physical or mental condition that prevents completing the questionnaires * Has a baby with congenital anomalies or chronic medical conditions * Has a premature or low-birth-weight baby * Has received infant care training within the last 6 months * Has adopted a child * Is outside the 19-65 age range

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Gaziantep Islam Science and Technology University Şahinbey Gaziantep

More Gaziantep Islam Science and Technology University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07295639 on ClinicalTrials.gov ↗ ← All trials in Turkey