- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06837350
Effects of Music on Post-Cesarean Pain, Anxiety, Breastfeeding and Mother Infant Attachment Impact
April 22, 2026 updated by: Nuran Nur AYPAR AKBAĞ, Sinop University
Music on Post-cesarean
The physiological effects of music therapy include creating a behavioral change and changing the mood by reducing psychophysiological stress, pain, anxiety and isolation.
Music has the ability to create deep relaxation.
It is known to have relieving effects on insomnia.
In addition, it has been reported that music therapy application before and during birth reduces labor pain and reduces postpartum anxiety and depression levels.
The postpartum period, which begins with the birth of the newborn, covers the 6-8 week period that it takes for the changes that occur in the woman's body during pregnancy to return to its pre-pregnancy state.
This period is an important transition period in which physical, social and emotional changes occur in mothers.
In addition to rapid anatomical and physiological changes, mothers experience a difficult process in which the transition to motherhood is experienced, new roles and responsibilities are assumed, and relationships with their spouses and other family members are reorganized.
Although a woman begins to feel the changes that having a baby creates in her daily life during pregnancy, she usually experiences the biggest change after the baby is born.
The period when the first emotional bond between the newborn and her family is formed and a sense of trust develops is defined as mother-baby bonding.
Many factors affect mother-baby bonding in the postpartum period, which is the most important time when the bond established between the expectant mother and the baby during pregnancy, referred to as prenatal bonding, is strengthened after birth.
It is particularly affected by the mother's upbringing, as well as her experiences during pregnancy, birth, puerperium, and the baby's first months.
Healthy and early interaction between mother and baby initiates a healthy bonding process.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
70
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 Contact
- Name: Nuran N Aypar Akbağ, PhD
- Phone Number: +905459141440
- Email: nnaypar@sinop.edu.tr
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
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being 18 years of age or older
- Being in the third trimester (up to 2 weeks before the planned cesarean delivery date)
- Being primigravida
- Having a single fetus
- Not having a hearing problem
- Voluntarily participating in the study
Exclusion Criteria:
- Having any chronic disease
- Having a risky pregnancy condition (gestational diabetes, gestational hypertension, preeclampsia, etc.)
- Having a psychiatric medical diagnosis and using medication.
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: control group
|
|
|
Experimental: music group
|
Listening to Turkish Music
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Visual Analog Scale (VAS)-pain
Time Frame: On the second day after C-section and the end of the 1st week postpartum, change from first pain level an average of 20 minutes.
|
Pain Level by Visual Analog Scale The patient marks the pain he/she feels on a scale of 10 cm (100 mm), pain point 1 means "no pain", pain point 10 means "worst pain possible."
|
On the second day after C-section and the end of the 1st week postpartum, change from first pain level an average of 20 minutes.
|
|
Postpartum Specific Anxiety Scale (PSAS)
Time Frame: On the second day after C-section and the end of the 1st week postpartum, change from first pain level an average of 30 minutes.
|
Anxiety Level by Postpartum Specific Anxiety Scale (PSAS).
The VAS-anxiety is a 10 cm line used to measure perceived anxiety intensity, with endpoints labeled "No Anxiety" and "Worst Anxiety Imaginable."
It meansthat those who score 73 and below on the scale have lowpostpartum anxiety levels, and those who score 101 andabove have a high level of anxiety.
|
On the second day after C-section and the end of the 1st week postpartum, change from first pain level an average of 30 minutes.
|
|
Mother and Newborn Information Form I and I
Time Frame: On the second day after C-section and end of the 1st postpartum week
|
It will be evaluated with the Mother and Newborn Information Form I and II created by the researchers.
Breastfeeding information will be assessed with this form.
|
On the second day after C-section and end of the 1st postpartum week
|
|
Mother Infant Attachment
Time Frame: On the second day after C-section and end of the 1st postpartum week
|
It will be evaluated with the Mother-Infant Attachment Scale.
The total score ranges from 0 to 24, with higher scores indicating lower mother-infant attachment.
|
On the second day after C-section and end of the 1st postpartum week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
April 23, 2026
Primary Completion (Estimated)
December 30, 2026
Study Completion (Estimated)
December 30, 2026
Study Registration Dates
First Submitted
January 17, 2025
First Submitted That Met QC Criteria
February 14, 2025
First Posted (Actual)
February 20, 2025
Study Record Updates
Last Update Posted (Actual)
April 28, 2026
Last Update Submitted That Met QC Criteria
April 22, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024/301
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Sharing is not considered appropriate until the article has completed its journal process and is published.
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.
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