Supportive Care During Childbirth & Well-being

Status Completed

Clinical Trial Summary

The aim of this study is to evaluate the effects of continuous supportive care (ICSC) at birth on some parameters of maternal psychological well-being.

Clinical Trial Description

This is a single-blind randomized controlled trial. Data were collected from 80 women who gave birth in the obstetrics clinic of a state hospital in the south of Turkey between December 2020 and June 2021. Participants who met the inclusion criteria were informed about the purpose of the study and the procedures to be performed, informed consent was obtained from those who agreed to participate, and women were assigned to the groups in line with a computer-based randomization program with an allocation ratio of 1:1. Block randomization could not be performed because of the different and long delivery processes. Data were collected in both groups at birth (latent phase, active phase, and transitional phase), within 24 hours of birth, and 6th-8th postpartum days after hospital admission and at least one hour of care. 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

Clinical Trial Details

NCT number	NCT05333653
Study type	Interventional
Source	Mersin University
Contact
Status	Completed
Phase	N/A
Start date	December 15, 2020
Completion date	June 27, 2021

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Supportive Care During Childbirth and Well-being

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms