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

Istanbul University - Cerrahpasa (IUC)

Status: Completed

Conditions: Continuous Birth Support

Treatments: Procedure: uninterrupted accompanying support

Study type: Interventional

Funder types: Other

Identifiers

NCT05720962

2022/401

Details and patient eligibility

About

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

Full 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.

Enrollment: 110 patients

Sex: Female

Ages: 18 to 35 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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110 participants in 2 patient groups

experimental group

Experimental group

Description:

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

Treatment:

Procedure: uninterrupted accompanying support

control group

No Intervention group

Description:

Only routine midwife support will be provided to the control group.