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Clinical Trials/NCT05380258
NCT05380258
Completed
Not Applicable

The Effect of Chewing Gum and Use of Stress Balls on Perception of Labor Pain, Fear of Birth, and Duration of Delivery

Kastamonu University1 site in 1 country96 target enrollmentMay 5, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Labor Pain
Sponsor
Kastamonu University
Enrollment
96
Locations
1
Primary Endpoint
labor pain
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This study was conducted as a randomized controlled experimental study. This study was planned to determine the effects of chewing gum and using a stress ball on the perception of labor pain, duration of labor and birth satisfaction. The population of the study consisted of primiparous mothers who applied to the hospital. This study was planned to determine the effects of chewing gum and using a stress ball on the perception of labor pain, duration of labor and birth satisfaction. The study was carried out in two stages. In the first stage, the data were collected in the delivery room, and in the second stage, the postpartum satisfaction levels of the mothers were measured in the postpartum service. The sample number of the investigators' study was determined as 96. Visual analog scale, birth satisfaction scale and birth follow-up form were used for the data of our study.

Registry
clinicaltrials.gov
Start Date
May 5, 2021
End Date
June 5, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Şahika ŞİMŞEK ÇETİNKAYA

Dr. Şahika ŞİMŞEK ÇETİNKAYA

Kastamonu University

Eligibility Criteria

Inclusion Criteria

  • Being primiparous to be in due time
  • To have spontaneous vaginal delivery
  • Ability to communicate verbally be between the ages of 18-35
  • Not having a risky pregnancy
  • Having a single fetus in the vertex position
  • Having started contractions and continuing regularly
  • Being in the latent phase of action (0-4 cm dilatation)
  • Not having used any analgesia or using any pain medication to reduce pain during labor

Exclusion Criteria

  • Mothers who have a cesarean section decision
  • Risky Pregnant
  • Multiple Pregnancies
  • Multiparous pregnant women

Outcomes

Primary Outcomes

labor pain

Time Frame: Visual Analog scale I for labor pain was applied in 0-3 cm , Visual Analog Scale II in 4-5 cm and Visual Analog Scale III was applied in 6-8 cm cervical dilatation. The study continues through study completion, an average of 1 year

Duration of labor

Time Frame: A birth follow-up form was used from the beginning of cervical dilatation to delivery.

birth satisfaction

Time Frame: satisfaction form used postpartum at the 4th hour

Study Sites (1)

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