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Father-Focused Breastfeeding Education and Breastfeeding Outcomes

Effect of a Short Postpartum Father-Focused Breastfeeding Education on Paternal Support Behaviors and Breastfeeding Outcomes at 1, 3, and 6 Months: A Randomized Controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07341256
Acronym
FBF-EDU
Enrollment
240
Registered
2026-01-14
Start date
2026-01-03
Completion date
2026-12-15
Last updated
2026-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breastfeeding, Exclusive Breastfeeding, Paternal Support

Keywords

Father-focused breastfeeding education, Paternal involvement, Breastfeeding outcomes, Partner Breastfeeding Influence Scale, Postpartum period

Brief summary

Breastfeeding is recommended as the optimal feeding method for infants during the first six months of life. Support from fathers or partners plays an important role in initiating and maintaining breastfeeding. However, most breastfeeding education programs mainly focus on mothers, and structured education directed to fathers is limited. This study aims to evaluate the effect of a short, structured, father-focused breastfeeding education given shortly after birth on paternal support behaviors and breastfeeding outcomes. Fathers of healthy term newborns will be randomly assigned to receive either a brief breastfeeding support education or routine care. Paternal support behaviors will be assessed using a validated questionnaire, and infant feeding outcomes will be evaluated during follow-up. The results of this study may help improve breastfeeding support strategies by involving fathers more actively in the early postnatal period.

Detailed description

This is a single-center, prospective, randomized controlled trial conducted at Sancaktepe Prof. Dr. Ilhan Varank Training and Research Hospital in Istanbul, Turkey. The study evaluates the impact of a short, structured, father-focused breastfeeding education delivered in the early postpartum period on paternal breastfeeding support behaviors and infant feeding outcomes. Fathers or partners of term, clinically stable newborns who are present in the hospital within 24 to 48 hours after birth and who provide written informed consent are eligible for participation. After baseline assessment, participants are randomized in a 1:1 ratio to either the intervention group or the control group. At baseline, sociodemographic data are collected, and paternal breastfeeding support behavior is assessed using the Turkish version of the Partner Breastfeeding Influence Scale (PBIS-TR). Fathers in the intervention group receive a brief, face-to-face breastfeeding support education lasting approximately 8 to 10 minutes. The education is based on international breastfeeding recommendations and focuses on practical ways fathers can support breastfeeding. The control group receives routine clinical care without additional intervention. Paternal breastfeeding support behavior is reassessed at one month postpartum. Infant feeding status is evaluated at 1, 3, and 6 months postpartum and categorized as exclusive breastfeeding, partial breastfeeding, or formula/other feeding. Data are analyzed to compare paternal support behaviors and breastfeeding outcomes between the two study groups. This study aims to provide evidence on the effectiveness of early, father-focused breastfeeding education in improving breastfeeding support and outcomes.

Interventions

BEHAVIORALFather-Focused Breastfeeding Education

A short, face-to-face educational session provided to fathers focusing on practical ways to support breastfeeding.

Sponsors

Timuçin İmdadoğlu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Participants are randomly assigned in parallel to either a father-focused breastfeeding education intervention or a control group receiving routine care.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Fathers or partners aged 18 years or older. * Fathers or partners of healthy term newborns (≥37 weeks gestation). * Newborns without major congenital anomalies or chronic medical conditions. * Fathers or partners present during the early postnatal period. * Ability to understand and communicate in Turkish. * Provision of written informed consent.

Exclusion criteria

* Fathers or partners of preterm infants (\<37 weeks gestation). * Newborns requiring neonatal intensive care unit admission. * Newborns with major congenital anomalies or severe medical conditions. * Fathers or partners unable to complete follow-up assessments. * Refusal or inability to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Paternal breastfeeding support behavior and exclusive breastfeeding at 1 month postpartum1 month postpartumPaternal breastfeeding support behavior will be assessed using the Turkish version of the Partner Breastfeeding Influence Scale (PBIS-TR). Infant feeding status at 1 month postpartum will be recorded and categorized as exclusive breastfeeding or non-exclusive breastfeeding.

Secondary

MeasureTime frameDescription
Infant feeding status at 3 months postpartum3 months postpartumInfant feeding status will be assessed at 3 months postpartum and categorized as exclusive breastfeeding, partial breastfeeding, or formula/other feeding.
Infant feeding status at 6 months postpartum6 months postpartumInfant feeding status will be assessed at 6 months postpartum and categorized as exclusive breastfeeding, partial breastfeeding, or formula/other feeding.

Countries

Turkey (Türkiye)

Contacts

Primary Contacttimucin imdadoglu, MD
dr.timucini@gmail.com+90 535 742 6892

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026