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Not yet recruiting NCT06837350

Effects of Music on Post-Cesarean Pain, Anxiety, Breastfeeding and Mother Infant Attachment Impact

No phase Interventional Cesarian Section Bonding Pain Anxiety

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An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Music intervention.
Who it may be relevant to
Registry conditions: Cesarian Section, Bonding, Pain, Anxiety. Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Music on Post-cesarean

Overview

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.

Interventions

  • Other Music intervention
    Listening to Turkish Music

Primary outcome measures

  • 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.]
  • 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.]
  • Mother and Newborn Information Form I and I [Time frame: 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]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06837350 · 2024/301

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗