The Effect of Musıc on Labor Paın, Anxıety and Breastfeedıng Success

August 6, 2026 updated by: Sibel ÖZTÜRK, Ataturk University

Effect of Musıc Lıstened to Prımarıparous Women Who Have Delıvered by Cesarean Sectıon on Paın, Status Anxıety and Breastfeedıng Success

The aim of this study is to examine the effects of music played to primiparous women who had a cesarean section on pain, state anxiety and breastfeeding success.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

65

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey (Türkiye)
    • Artuklu/Mardin
      • Mardin, Artuklu/Mardin, Turkey (Türkiye), 47050
        • Mardin Education and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Caesarean section
  • Live birth

Exclusion Criteria:

  • Risky pregnancy
  • Twin pregnancy
  • Newborn with cleft palate, cleft lip

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Vsisual Analog scale (VAS)
It will be used to measure pain in the intervention and control groups during the postpartum period.
Behavioral: Music
Listen to Music
Experimental: State anxiety scale
It will be used to evaluate the mother's current anxiety status in the postpartum period.
Behavioral: Music
Listen to Music
Experimental: Breastfeedıng Success
It will be used to evaluate the breastfeeding success of mothers in the experimental and control groups in the postpartum period.
Behavioral: Music
Listen to Music

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postpartum Pain
Time Frame: Within the first hour after birth
The Visual Analog Scale will be used to assess the level of cesarean pain in the postpartum period in the intervention and control groups. A minimum score of 1 and a maximum score of 10 are obtained from the scale. As the score obtained from the scale increases, it indicates that the pain also increases. After the pre-test and intervention, a change in pain and a change in the Visual Analog Scale score are expected in the intervention group.
Within the first hour after birth
State Anxiety
Time Frame: Within the first hour after birth
The state anxiety scale evaluates the degree of severity of the emotions or behaviors experienced by the individual in the situation he/she is in. The highest score that can be obtained is 80, and the lowest score is 20. As the score obtained from the scale increases, it shows that the state anxiety also increases.
Within the first hour after birth
Breastfeeding Success
Time Frame: Within the first hour after birth
The scale evaluates the success of mothers in breastfeeding their babies. The minimum score that can be obtained from the scale is 0 and the maximum score is 10, and a high score from the evaluation and diagnosis scale means that breastfeeding success is high.
Within the first hour after birth

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Ataturk University

Investigators

  • Principal Investigator: Sibel ÖZTÜRK, PhD, sibel.ozturk@atauni.edu.tr
  • Principal Investigator: Ayşegül ŞAHİSN ÇELEBİ, PhD, ascelebi@beu.edu.tr

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 13, 2026

Primary Completion (Actual)

March 30, 2026

Study Completion (Actual)

May 26, 2026

Study Registration Dates

First Submitted

September 23, 2024

First Submitted That Met QC Criteria

September 27, 2024

First Posted (Actual)

October 1, 2024

Study Record Updates

Last Update Posted (Actual)

August 10, 2026

Last Update Submitted That Met QC Criteria

August 6, 2026

Last Verified

August 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Ataturk University SOZTURK0005

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Subscribe