Selcuk University
Konya, 42100, Turkey (Türkiye)
NCT Number: NCT07164521
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.
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Notify Me18 year–45 year
Female
Interventional
Not applicable
Konya, 42100, Turkey (Türkiye)
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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
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
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.
Other names: Experimental - Music Listening
Time frame: 48th postpartum hour
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
Measured using the Pain Catastrophizing Scale (PCS) at the 48th postpartum hour. Higher scores indicate greater pain catastrophizing.
Time frame: Between the 24th and 48th postpartum hour
Total number of minutes of music listened by participants in the intervention group across the intervention period.
Selcuk University
Other
The Effect of Music Played During the Postoperative Period on Pain and Anxiety Levels in Women Who Underwent Cesarean Delivery: A Randomized Controlled Trial
Acronym: EMPP
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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