Effect of Listening to Surah Al-Inshirah (The Opening-Up of the Heart) After Cesarean Birth on Postpartum Outcomes
The Effect of Listening to Surah Al-Inshirah (The Opening-Up of the Heart) in the Early Postpartum Period After Cesarean Birth on Women's Spiritual Well-Being, Depression, and Maternal Attachment: A Randomized Controlled Trial
1 other identifier
interventional
172
1 country
1
Brief Summary
This randomized controlled trial aims to evaluate the effect of listening to the recitation of Surah Al-Inshirah during the early postpartum period after cesarean birth on women's spiritual well-being, depression levels, and maternal attachment. The postpartum period is a sensitive phase characterized by physical recovery, emotional changes, and adaptation to the maternal role, particularly following cesarean delivery. Spiritual and religious practices are commonly used as coping strategies in this period, especially in Muslim populations. In this study, women who have undergone cesarean birth will be randomly assigned to either an intervention group or a control group. The intervention group will listen to the recitation of Surah Al-Inshirah in addition to receiving routine postpartum care, while the control group will receive routine postpartum care only. Outcomes related to spiritual well-being, postpartum depression, and maternal attachment will be assessed within the first 48 hours after birth. The findings of this study are expected to contribute to evidence-based, culturally sensitive, and low-cost supportive care practices in the early postpartum period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2026
CompletedFirst Submitted
Initial submission to the registry
January 12, 2026
CompletedFirst Posted
Study publicly available on registry
January 21, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
March 5, 2026
March 1, 2026
11 months
January 12, 2026
March 3, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Postpartum Depression Level
Postpartum depression will be assessed using the Edinburgh Postnatal Depression Scale (EPDS), a validated self-report questionnaire measuring depressive symptoms in the postpartum period. Higher scores indicate higher levels of depressive symptoms. The EPDS is a validated 10-item self-report questionnaire assessing depressive symptoms in the postpartum period. Each item is scored on a 4-point scale (0-3). Total scores range from 0 to 30, with higher scores indicating more severe depressive symptoms.
Within the first 48 hours postpartum
Secondary Outcomes (2)
Spiritual Well-Being
Within the first 48 hours postpartum
Maternal Attachment
Within the first 48 hours postpartum
Study Arms (2)
Experimental: Surah Al-Inshirah Listening Group
EXPERIMENTALParticipants in this group will receive routine postpartum care and will additionally listen to an audio recording of Surah Al-Inshirah during the early postpartum period following cesarean birth.
Control
NO INTERVENTIONParticipants in this group will receive routine postpartum care only, without any additional audio or spiritual intervention.
Interventions
Participants will listen to a standardized audio recording of Surah Al-Inshirah in a quiet and comfortable environment during the first 48 hours after cesarean birth, in addition to routine postpartum care.
Eligibility Criteria
You may qualify if:
- Being literate
- Able to speak and understand Turkish
- Aged 18 years or older
- Primiparous women
- Having undergone cesarean birth
- Gestational age at birth between 37 and 42 weeks
- Identifying as Muslim
- Willing to participate voluntarily after providing written informed consent
- Women who have given birth within the last 48 hours and are hospitalized during the early postpartum period
You may not qualify if:
- Having a diagnosed psychiatric disorder
- Newborn admitted to the neonatal intensive care unit
- Experiencing stillbirth
- Having a hearing impairment
- Criteria for Withdrawal From the Study
- Development of obstetric complications for any reason during the study
- Requesting to withdraw from the study during the data collection process
- Reporting feeling unwell or uncomfortable during the data collection process
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Selçuk University
Konya, Selçuklu, 42130, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This is an open-label study. Due to the nature of the audio-based spiritual intervention, participants and researchers are aware of group assignment.
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assoc. Dr.
Study Record Dates
First Submitted
January 12, 2026
First Posted
January 21, 2026
Study Start
January 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
March 5, 2026
Record last verified: 2026-03