NCT07460921

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
110

participants targeted

Target at P50-P75 for not_applicable

Timeline
7mo left

Started Mar 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress34%
Mar 2026Dec 2026

First Submitted

Initial submission to the registry

March 5, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

March 5, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 10, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2026

Expected
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

March 10, 2026

Status Verified

March 1, 2026

Enrollment Period

5 months

First QC Date

March 5, 2026

Last Update Submit

March 5, 2026

Conditions

Keywords

PodcastPostpartum womanDepressionMaternal attachmentSelf-care

Outcome Measures

Primary Outcomes (4)

  • 1. Introductory Information Form

    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

    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

    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

    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 Outcomes (3)

  • The Edinburgh Postnatal Depression Scale

    5 minutes

  • Maternal Attachment Scale

    10 minutes

  • Self-Care Agency Scale

    10 minutes

Study Arms (2)

Experimental: İntervention group

EXPERIMENTAL

In addition to routine discharge care, 5-6 minute podcasts consisting of 4 modules of discharge education were played.

Other: Providing discharge education via podcasts

No Intervention: Control group

NO INTERVENTION

Routine discharge care

Interventions

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.

Experimental: İntervention group

Eligibility Criteria

Age19 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Depression

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Central Study Contacts

Yasemin AYDIN KARTAL, PROF.DR.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Randomized Controlled Experimental Design
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PROF.DR

Study Record Dates

First Submitted

March 5, 2026

First Posted

March 10, 2026

Study Start

March 5, 2026

Primary Completion (Estimated)

July 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

March 10, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share