- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07460921
The Effect of Podcast Education on Postpartum Depression, Maternal Attachment, and Self-Care Agency in the Early Postpartum Period: A Randomized Controlled Trial
March 5, 2026 updated by: YASEMİN AYDIN KARTAL, Saglik Bilimleri Universitesi
The population of the study, planned as a randomized controlled experimental design, consists of primiparous women who gave birth in the delivery unit of Istanbul Esenler Women's Health and Pediatric Diseases Hospital.
The sample of the study will be composed of 110 postpartum women who meet the sampling criteria, are willing to participate, and are determined by power analysis.
The study includes two groups: the "intervention group (n=55)," who will receive discharge education through podcasts in the early postpartum period, and the "control group (n=55)," who will receive routine discharge education.
Women in the intervention group will listen to four podcasts, each lasting 5-6 minutes, about discharge education during the early postpartum period.
Before the data collection forms are applied, participants will be asked to complete an "Informed Consent Form."
All groups will be evaluated with the "Edinburgh Postpartum Depression Scale," the "Maternal Attachment Scale," and the "Self-Care Agency Scale" both before and after the intervention.
The discussion and conclusions of the study will be written based on the results obtained.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
110
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yasemin AYDIN KARTAL, PROF.DR.
- Phone Number: (0216) 777 87 77
- Email: yasemin.aydin@sbu.edu.tr
Study Contact Backup
- Name: Ayşegül AKDEMİR
- Phone Number: (0216) 777 87 77
- Email: aysegulakdemir05@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Volunteering to participate in the study
- Being primigravida
- Being over the age of 19
- Giving birth in the delivery unit of Esenler Maternity and Children's Hospital
- Being able to speak and understand Turkish
- Being literate
- Having a live and singleton birth
Exclusion Criteria:
- Unwillingness to participate in the study
- Having a psychiatric diagnosis and/or using psychiatric medication
- Being an adolescent mother
- Being a high-risk postpartum woman
- Having a high-risk newborn
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental: İntervention group
In addition to routine discharge care, 5-6 minute podcasts consisting of 4 modules of discharge education were played.
|
In addition to the routine discharge education, the postpartum women assigned to the intervention group will listen to a discharge training podcast consisting of 4 modules, each lasting 5-6 minutes, via a Xiaomi Poco X3 phone.
|
|
No Intervention: No Intervention: Control group
Routine discharge care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
1. Introductory Information Form
Time Frame: 5 Minutes
|
A data collection form was developed by the researchers based on a review of the relevant literature.
The form includes items designed to assess the socio-demographic and obstetric characteristics of primiparous postpartum women.
Socio-demographic variables include age, educational level, family structure, and income status.
Obstetric variables include mode of delivery, receipt of prenatal education, use of postpartum contraceptive methods, and whether the pregnancy was planned.
|
5 Minutes
|
|
The Edinburgh Postnatal Depression Scale
Time Frame: 5 minutes
|
The Edinburgh Postnatal Depression Scale (EPDS) was developed by Cox et al. in 1987 to screen for depression during the postpartum period (26).
The Turkish validity and reliability study of the scale was conducted by Engindeniz et al. in 1997.
The Cronbach's alpha coefficient of the scale was found to be 0.79.
The EPDS is a self-report instrument consisting of 10 items in a 4-point Likert-type format.
Each item is scored between 0 and 3.
The total score ranges from a minimum of 0 to a maximum of 30.
|
5 minutes
|
|
Maternal Attachment Scale
Time Frame: 10 minutes
|
The Maternal Attachment Scale (MAS) was developed by Muller in 1994 to measure maternal attachment.
The Turkish validity and reliability study was conducted by Kavlak and Şirin in 2009.
The MAS assesses maternal feelings and behaviors that show affection.
Since it is a self-report scale, the person completing it must be literate and able to understand what they read.
The scale consists of 26 items with a 4-point Likert scale, offering the options "always," "frequently," "sometimes," and "never."
The scoring is: always = 4 points, frequently = 3 points, sometimes = 2 points, and never = 1 point.
Scores range from 26 to 104, with higher scores indicating stronger maternal attachment.
The Cronbach's alpha value was found to be 0.77 for mothers with one-month-old babies and 0.82 for mothers with four-month-old babies.
|
10 minutes
|
|
Self-Care Agency Scale
Time Frame: 10 minutes
|
The Self-Care Agency Scale was developed by Kearney and Fleischer in 1979 to measure individuals' ability to care for themselves.
The Turkish validity and reliability study was done by Nahçıvan in 1994.
The scale has 35 items with a 5-point Likert format: "does not describe me at all," "does not describe me well," "undecided," "describes me somewhat," and "describes me very well."
Scores range from 0 to 4 accordingly.
Eight items (3, 6, 9, 13, 19, 22, 26, 31) are reverse scored.
Positive items are scored 0-4; negative items 4-0.
Scores ≤82 indicate low, 83-120 moderate, and >120 high self-care agency.
Cronbach's alpha was 0.89.
|
10 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Edinburgh Postnatal Depression Scale
Time Frame: 5 minutes
|
Description: The Edinburgh Postnatal Depression Scale (EPDS) was developed by Cox et al. in 1987 to screen for depression during the postpartum period (26).
The Turkish validity and reliability study of the scale was conducted by Engindeniz et al. in 1997.
The Cronbach's alpha coefficient of the scale was found to be 0.79.
The EPDS is a self-report instrument consisting of 10 items in a 4-point Likert-type format.
Each item is scored between 0 and 3.
The total score ranges from a minimum of 0 to a maximum of 30.
|
5 minutes
|
|
Maternal Attachment Scale
Time Frame: 10 minutes
|
Description: The Maternal Attachment Scale (MAS) was developed by Muller in 1994 to measure maternal attachment.
The Turkish validity and reliability study was conducted by Kavlak and Şirin in 2009.
The MAS assesses maternal feelings and behaviors that show affection.
Since it is a self-report scale, the person completing it must be literate and able to understand what they read.
The scale consists of 26 items with a 4-point Likert scale, offering the options "always," "frequently," "sometimes," and "never."
The scoring is: always = 4 points, frequently = 3 points, sometimes = 2 points, and never = 1 point.
Scores range from 26 to 104, with higher scores indicating stronger maternal attachment.
The Cronbach's alpha value was found to be 0.77 for mothers with one-month-old babies and 0.82 for mothers with four-month-old babies.
|
10 minutes
|
|
Self-Care Agency Scale
Time Frame: 10 minutes
|
Description: The Self-Care Agency Scale was developed by Kearney and Fleischer in 1979 to measure individuals' ability to care for themselves.
The Turkish validity and reliability study was done by Nahçıvan in 1994.
The scale has 35 items with a 5-point Likert format: "does not describe me at all," "does not describe me well," "undecided," "describes me somewhat," and "describes me very well."
Scores range from 0 to 4 accordingly.
Eight items (3, 6, 9, 13, 19, 22, 26, 31) are reverse scored.
Positive items are scored 0-4; negative items 4-0.
Scores ≤82 indicate low, 83-120 moderate, and >120 high self-care agency.
Cronbach's alpha was 0.89.
|
10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
March 5, 2026
Primary Completion (Estimated)
July 31, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
March 5, 2026
First Submitted That Met QC Criteria
March 5, 2026
First Posted (Actual)
March 10, 2026
Study Record Updates
Last Update Posted (Actual)
March 10, 2026
Last Update Submitted That Met QC Criteria
March 5, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SBU-AYDINKARTAL-AKDEMİR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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