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Clinical Trial Summary

The aim of this study was to determine the effect of postpartum skin-to-skin contact time on fear of childbirth, birth trauma and maternal attachment.


Clinical Trial Description

This is a single-blind, randomized controlled trial. Data were collected from 110 women who gave birth in the gynecology clinic of a public hospital in southern Turkey between September 2021 and February 2022. Participants who met the inclusion criteria were informed about the purpose of the study and skin-to-skin contact, informed consent was obtained from those who agreed to participate, and the women were divided into groups according to a 1:1 computer-based randomization program. Data were collected at the time of consent to the study, within the first hour after birth, 24 hours after birth, 4 weeks postpartum, and 4 months postpartum. Collected by the first author. The CONSORT directive was followed in the planning, implementation and writing of the research. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05479955
Study type Interventional
Source Mersin University
Contact
Status Completed
Phase N/A
Start date September 1, 2021
Completion date February 17, 2022

See also
  Status Clinical Trial Phase
Completed NCT04425096 - The Effect of Skin to Skin Contact on Postpartum Hemorrhage, Pain And Breastfeeding N/A
Completed NCT02143193 - Skin-to Skin Contact on Newborn Temperature N/A