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CompletedNCT07164521EMPPUpdated Sep 10, 2025

The Effect of Music Postoperative Period

An interventional study of Music Listening (Relaxing Classical Music) in Cesarean Section; Dehiscence and Postoperative Pain, sponsored by Selcuk University. Completed at 1 site in Turkey (Türkiye). Open to female participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-09-10.

Sponsored by Selcuk University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Feb 2024, registered Aug 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
110
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
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Study summary

This randomized controlled trial aimed to evaluate the effects of music listening on anxiety and pain among women following cesarean delivery. A total of 110 women who had undergone cesarean section were included. Beginning at the 24th postpartum hour, participants in the intervention group listened to relaxing classical music for 15 minutes every hour, while no intervention was applied to the control group. The study was designed to determine whether music listening could influence postpartum anxiety and perceived pain.

Read the detailed description

Postpartum women undergoing cesarean section often experience significant levels of anxiety and pain, which can negatively affect recovery and maternal-infant bonding. In addition to pharmacological methods, non-pharmacological strategies such as music listening may play an important role in supporting women during this period. In this study, 110 women who had undergone cesarean delivery were randomly assigned to intervention and control groups. Starting at the 24th postpartum hour until the 48th hour, women in the intervention group listened to relaxing classical instrumental music (e.g., works by Mozart, Vivaldi, and Debussy) for 15 minutes every hour. The control group received no intervention. Participants' demographic and clinical characteristics were collected using the Descriptive Characteristics Form, while postpartum anxiety and pain perception were assessed with the Postpartum-Specific Anxiety Scale (PSAS) and Pain Catastrophizing Scale (PCS). The primary outcome was anxiety, and the secondary outcome was pain perception. The study sought to assess whether a music-based, culturally appropriate, non-pharmacological intervention could be an effective component of routine postpartum care following cesarean delivery.

02

Conditions studied

  • Cesarean Section; Dehiscence
  • Postoperative Pain

Keywords

  • Postoperative Pain
  • Cesarean Section
  • Anxiety
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In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's enrollment of 110 is above the median of 75 across 4,344 interventional studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Selcuk University is the lead sponsor of 248 studies on the registry; 63 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Women aged 18 years or older

Primiparous (first-time mothers)

Underwent cesarean section under spinal anesthesia

Mentally healthy and able to communicate

No hearing impairments (able to hear the music intervention)

No chronic illnesses

No complications during labor for mother or newborn

Proficient in Turkish

Voluntarily agreed to participate and provided informed consent

Exclusion criteria

Exclusion Criteria:

Multiparous women (previous childbirth experience)

Women who used non-routine analgesics beyond standard postpartum pain relievers

Presence of psychiatric disorders or severe mental illness

Medical complications during or after delivery for mother or infant

Hearing impairments preventing participation in music listening

Women unwilling or unable to comply with the intervention protocol

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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
110 participants (actual)

Study arms

  • Experimental
    Experimental - Music Listening

    Women in the intervention group listened to relaxing classical instrumental music (e.g., works by Mozart, Vivaldi, and Debussy) for 15 minutes every hour, starting at the 24th postpartum hour until the 48th hour.

    Behavioral: Music Listening (Relaxing Classical Music)

  • No intervention
    No Intervention - Control

    Women in the control group received routine postpartum care without any additional intervention.

Interventions

  • BehavioralMusic Listening (Relaxing Classical Music)

    Participants listened to a standardized playlist of relaxing classical instrumental music (e.g., Mozart, Vivaldi, Debussy) for 15 minutes every hour, beginning at the 24th postpartum hour until the 48th hour. The intervention aimed to reduce postpartum anxiety and pain perception.

    Also known as: Experimental - Music Listening

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What researchers measure

Primary outcomes

  1. Postpartum Anxiety

    Measured using the Postpartum-Specific Anxiety Scale (PSAS) at the 48th postpartum hour. Higher scores indicate higher levels of anxiety.

    Time frame: 48th postpartum hour

  2. Pain Catastrophizing

    Measured using the Pain Catastrophizing Scale (PCS) at the 48th postpartum hour. Higher scores indicate greater pain catastrophizing.

    Time frame: 48th postpartum hour

Secondary outcomes

  1. Total Duration of Music Listening

    Total number of minutes of music listened by participants in the intervention group across the intervention period.

    Time frame: Between the 24th and 48th postpartum hour

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Study locations

1 site
  • Selcuk University
    Konya, 42100, Turkey (Türkiye)
08

References and documents

Publications

  • Akin B, Ozdemir S. The Effect of Music Played During the Postoperative Period on Pain and Anxiety Levels in Women Who Underwent Cesarean Delivery: A Randomized Controlled Trial. J Integr Complement Med. 2026 Mar;32(3):296-302. doi: 10.1177/27683605251389490. Epub 2025 Oct 28. PubMed 41182331 ↗

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 10, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07164521
Lead sponsor
Selcuk University
Responsible party
Bihter Akın (Assoc. Prof., Selcuk University) — Principal investigator
First posted
Sep 10, 2025
Start date
Feb 1, 2024
Primary completion
Jul 30, 2024
Completion
Jul 31, 2024
Last update
Sep 10, 2025

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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