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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.
Full 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.
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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
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110 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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