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Clinical Trials in Turkey / NCT07656207
Starting soon Not applicable

The Effect of Skin-to-skin Contact at Birth

NCT07656207 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-07
Last updated
2026-06-18

Condition(s) studied

Midwifery SupportSkin to Skin ContactParenthood Status

Investigational drug(s) / intervention(s)

Immediate skin-to-skin contact after birth (intervention group)

Immediate skin-to-skin contact after birth (intervention group): Immediate skin-to-skin contact after birth: If the newborn requires no intervention, they will be immediately placed on the mother's chest (before cord clamping) and skin-to-skin contact will begin. Skin-to-skin contact will be maintained for approximately 60 minutes until the first breastfeeding occurs. All routine procedures performed in the delivery room for the newborn (except for weight measurement) will be performed while the newborn is on the mother's chest.

Study summary

To determine the effects of skin-to-skin contact at birth on birth outcomes (placental delivery time, postpartum pain level, time of first breastfeeding, and breastfeeding motivation) and on postpartum parenting behavior.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Vaginal delivery * Primiparous pregnancy * Delivery at 37 weeks or later * Single, live fetus * Not a high-risk pregnancy * Not an individual with special needs * Able to communicate Exclusion Criteria: * Women who Have a multiple pregnancy, * Develop complications requiring emergency intervention in the mother or baby after delivery, * Have their baby admitted to the neonatal intensive care unit after delivery, * Have a cesarean section, * Withdraw from the study will be excluded from the research.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tarsus University Toroslar Mersin

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 NCT07656207 on ClinicalTrials.gov ↗ ← All trials in Turkey