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Ukulele Music on Pain, Anxiety, and Postpartum Comfort

NCT07786558 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2026-08-26

No results posted yet for this study

Summary

This study aims to examine whether listening to live ukulele music after cesarean delivery can help reduce pain-related distress and anxiety and improve comfort in women who have given birth by cesarean section for the first time.

Women participating in the study will be randomly assigned to either a ukulele music group or a routine care group. Women in the ukulele music group will listen to live ukulele music for 30 minutes at 24 hours after cesarean delivery. Women in the routine care group will receive the usual care provided by the hospital.

The study will compare the two groups in terms of pain-related thoughts and distress, postpartum anxiety, and overall comfort during the early postpartum period. The findings may help determine whether live ukulele music can be used as a simple, non-drug approach to support women during recovery after cesarean delivery.

Conditions

  • Postpartum

Interventions

BEHAVIORAL

Live Ukulele Music

Women who were admitted to the postoperative unit and met the eligibility criteria were assessed by the researcher. Eligible women were provided with written and verbal information about the purpose of the study, the intervention procedures, ethical and institutional permissions, and the confidentiality of personal information. Written informed consent was obtained from women who agreed to participate in the study. Participants were assigned to the intervention and control groups in a 1:1 ratio using a computer-generated randomization sequence created with the RANDOM.ORG Sequence Generator (RANDOM.ORG, 2026). After the Informed Consent Form and Introductory Characteristics Questionnaire were administered to women assigned to the intervention group, the same standardized melody was performed live on the ukulele by the researcher for 30 minutes at 24 hours postoperatively. Following the intervention, the Postpartum Specific Anxiety Scale, Postpartum Comfort Scale, and Pain Catastrophizin

Sponsors & Collaborators

  • Selcuk University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-03-05
Primary Completion
2025-09-01
Completion
2025-09-05

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07786558 on ClinicalTrials.gov