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Clinical Trials/NCT03066973
NCT03066973CompletedNot Applicable

THE EFFECTIVENESS OF BREATHING EXERCISES TO LABOR PAIN and DURATION: A RANDOMIZED CONTROLLED TRIAL

Ataturk University0 sites250 target enrollmentStarted: May 1, 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
250
Primary Endpoint
Labor pain

Study Overview

Brief Summary

This study aimed to assess the efficacy of breathing exercises (BE) during the second stage of labor for maternal pain, duration of labor and first-minute APGAR score. This is a randomized controlled trial that compares nulliparous pregnant in the second stage of labor instructed regarding BE with a control group (CG) that received standard care service. It was conducted at Nenehatun Obstetric and Gynecology Hospital between May-June 2016, in Erzurum. One session of BE training were given to pregnant in intervention group (IG). Visual Analog Scale (VAS) was performed to identify perception of pain to all pregnant during the second stage of birth. Time of the second stage was recorded as second (sec), and first minute APGAR scores were recorded. Significance was set at p<0.05.

Detailed Description

In this trial, it is aimed to assess the effectiveness of breathing exercises (BE) for management of labor pain during the second stage of labor. Nulliparous pregnant were randomized two arms. Intervention group received breathing exercise at the first stage of labor. Control group received routine care services. It was conducted at Nenehatun Obstetric and Gynecology Hospital between May-June 2016, in Erzurum, Turkey. Visual Analog Scale (VAS) was performed to identify perception of pain to all pregnant during the second stage of labor. Time of the second stage was recorded as second (sec), and first minute APGAR scores of newborn were recorded. All analysis was carried out using SPSS 20. Significance was set at p<0.05.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Nullipar females
  • Gestational age 37-42 week

Exclusion Criteria

  • Analgesic and anestezice use
  • Clinical instability
  • Psychiatric disorders

Outcomes

Primary Outcomes

Labor pain

Time Frame: 1 MONTH

It will be measured by Visual Analog Scale (VAS)

Secondary Outcomes

  • APGAR score(1 MONTH)
  • Duration of labor(1 MONTH)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Yasemin Cayir

Assoc. Prof.

Ataturk University

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