NCT07354334

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
172

participants targeted

Target at P75+ for not_applicable

Timeline
7mo left

Started Jan 2026

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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 Progress38%
Jan 2026Dec 2026

Study Start

First participant enrolled

January 1, 2026

Completed
11 days until next milestone

First Submitted

Initial submission to the registry

January 12, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 21, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

March 5, 2026

Status Verified

March 1, 2026

Enrollment Period

11 months

First QC Date

January 12, 2026

Last Update Submit

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

EXPERIMENTAL

Participants 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.

Behavioral: Listening to Surah Al-Inshirah

Control

NO INTERVENTION

Participants 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.

Experimental: Surah Al-Inshirah Listening Group

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

MeSH Terms

Conditions

Depression, Postpartum

Condition Hierarchy (Ancestors)

Puerperal DisordersPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesDepressive DisorderMood DisordersMental Disorders

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
Model Details: Participants will be randomly assigned to either an intervention group receiving routine postpartum care plus listening to Surah Al-Inshirah or a control group receiving routine postpartum care only.
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

Locations