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Clinical Trials in Turkey / NCT07396415
Starting soon Not applicable

Telehealth-Supported Breastfeeding Counseling in Primiparous Mothers

NCT07396415 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-02-25
Last updated
2026-02-09

Condition(s) studied

BreastfeedingPostpartum Depression (PPD)Breastfeeding Self-Efficacy

Investigational drug(s) / intervention(s)

Telehealth-Supported Breastfeeding CounselingRoutine Postpartum Care

Telehealth-Supported Breastfeeding Counseling: Structured breastfeeding counseling delivered via telehealth methods, including scheduled video or telephone-based sessions conducted by trained healthcare professionals. The intervention is provided in addition to routine postpartum care and focuses on breastfeeding techniques, problem-solving, maternal support, and breastfeeding self-efficacy during the postpartum period.

Routine Postpartum Care: Participants receive routine postpartum care according to standard clinical practice, without additional telehealth-supported breastfeeding counseling.

Study summary

Breastfeeding is critical for infant and maternal health; however, many first-time mothers experience difficulties that may lead to early discontinuation of breastfeeding. Telehealth-supported breastfeeding counseling has the potential to provide timely, accessible, and continuous support to mothers during the postpartum period.

This randomized controlled trial aims to evaluate the effect of telehealth-supported breastfeeding counseling on breastfeeding duration, breastfeeding self-efficacy, and postpartum depressive symptoms in primiparous mothers. Participants will be randomly assigned to either a telehealth-supported breastfeeding counseling group or a routine postpartum care group.

The intervention group will receive structured breastfeeding counseling sessions delivered via telecommunication tools in addition to standard care, while the control group will receive routine postpartum care only. Outcomes will be assessed using validated questionnaires and follow-up evaluations during the postpartum period. The findings of this study may contribute to improving breastfeeding support strategies and maternal mental health outcomes.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Primiparous women aged 18-45 years. * Mothers who have delivered a healthy, term (≥37 weeks), singleton infant. * Ability to communicate in Turkish. * Willingness to participate in the study and provide informed consent. * Access to a telephone or internet-enabled device for telehealth communication. Exclusion Criteria: * Mothers with severe maternal medical or psychiatric conditions that may interfere with breastfeeding. * Infants with congenital anomalies or conditions affecting feeding. * Mothers who require neonatal intensive care admission for their infants. * Mothers who are unable to participate in telehealth follow-up.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Marmara University Faculty of Medicine Istanbul Turkey (Türkiye)

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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 NCT07396415 on ClinicalTrials.gov ↗ ← All trials in Turkey