The Effect of Continuous Accompanying Support in the Active Phase on Labor Pain, Duration and Satisfaction

Not Applicable

Completed

• Conditions: Continuous Birth Support
• Interventions: Procedure: uninterrupted accompanying support

• Registration Number: NCT05720962
• Lead Sponsor: Istanbul University - Cerrahpasa (IUC)

Brief Summary

This study was planned to determine the effect of continuous accompanying support during the active phase on labor pain, duration and satisfaction.

Detailed Description

Participants who comes into childbirth needs the support of people around her in order to cope with the stress, anxiety and labor pain she experiences. This support is the continuous birth support given from the time the participants comes to the hospital until the birth of the baby. Having someone who supports the woman during the birth process will provide a positive birth experience for pregnant women. At the same time, the feeling of pain of the supported woman will be reduced and the delivery time will be shortened.

This randomized controlled study was planned to be performed on primiparous pregnant women between January 2023 and January 2024. The data of the study will be collected with "Personal Information Form", "Visual Analog Scale".

The study was divided into two groups as experimental and control groups. 55 participants in the experiment -55 participants will be randomized to the control group. Participants meeting the inclusion criteria will be asked to rate their pain and satisfaction from 0 to 10 with the VAS 4 cm, 6 cm, 8 cm and fully open. While both groups receive routine midwife support, when the experimental group reaches 4 cm, a person they want will be taken with them and continuous support will be given until there is a dilation of 10 cm.

Study Timeline

• Study Start: 2023-01-01
• Study First Submitted: 2023-01-23
• Study First Submitted QC: 2023-01-31
• Study First Posted: 2023-02-09
• Primary Completion: 2024-01-01
• Status Verified: 2024-03
• Study Completion: 2024-03-01
• Last Update Submitted: 2024-03-04
• Last Update Posted: 2024-03-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 110

Inclusion Criteria

• 18-35 years old
• Being literate
• Fluent and speaking Turkish
• Primiparous
• Spontaneous vaginal delivery planned
• At the beginning of the active phase (dilatation 4 cm)
• Pregnant women who agreed to participate in the research

Exclusion Criteria

• Presence of a health problem in the mother during pregnancy
• At risk of fetal anomaly
• Having multiple pregnancy
• Administering analgesic medication during labor

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
experimental group	uninterrupted accompanying support	The experimental group will be provided with routine midwife support and uninterrupted accompanying support.

Primary Outcome Measures

Name	Time	Method
Personal information form	"through study completion, an average of 1 year".	It is a form that includes questions that determine socio-demographic characteristics and perception of support. The form also includes questions about the process of the birth period.
Visual Analog Scale (VAS)	"through study completion, an average of 1 year"	It is a reliable and easily applicable scale accepted in the world literature. It is used to measure the values that cannot be measured numerically in the evaluation of the pain intensity and satisfaction of the patients. A minimum of 0 and a maximum of 10 points can be obtained from the scale. Additionally, higher scores indicate higher pain intensity, higher satisfaction.

Trial Locations

Locations (1)

Istanbul Universty Cerrahpaşa; 🇹🇷 Istanbul, Turkey