Podcast-Supported Prenatal Education Based on the Health Promotion Model
PPE-HPM
The Effect of Podcast-Supported Prenatal Education Based on the Health Promotion Model on the Empowerment, Healthy Lifestyle Behaviors, and Quality of Life of Pregnant Women
1 other identifier
interventional
60
1 country
2
Brief Summary
This randomized controlled trial aims to evaluate the effect of podcast-supported prenatal education based on the Health Promotion Model on empowerment, healthy lifestyle behaviors, and quality of life among pregnant women. A total of 60 pregnant women at 8-12 weeks of gestation who meet the eligibility criteria will be included in the study and randomly assigned to an intervention group (n=30) or a control group (n=30) using block randomization. At baseline, participants in both groups will complete a Descriptive Information Form, the Healthy Lifestyle Behaviors Scale in Pregnancy, the Pregnant Women Empowerment Scale, and the Pregnancy Quality of Life Scale. Following the baseline assessment, participants will be informed about the study process and the intervention schedule. Participants in the intervention group will receive a four-week online prenatal education program based on the Health Promotion Model, consisting of eight educational modules delivered twice a week. After each educational session, a podcast related to the session content will be shared with the participants. During the intervention period, participants will also receive reminders to listen to the podcasts and motivational messages to support their participation in the program. Participants in the control group will receive routine prenatal care and will be included in a WhatsApp group for communication related to the study. They will not receive the podcast-supported prenatal education program during the intervention period. The Healthy Lifestyle Behaviors Scale in Pregnancy, Pregnant Women Empowerment Scale, and Pregnancy Quality of Life Scale will be administered to participants at three time points: baseline at 8-12 weeks of gestation, immediately after completion of the educational intervention at 20 weeks of gestation, and at 32 weeks of gestation. Changes in empowerment, healthy lifestyle behaviors, and quality of life will be compared between the intervention and control groups.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable pregnancy
Started Dec 2026
Shorter than P25 for not_applicable pregnancy
2 active sites
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
First Submitted
Initial submission to the registry
September 6, 2026
CompletedFirst Posted
Study publicly available on registry
September 11, 2026
CompletedStudy Start
First participant enrolled
December 15, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2027
Study Completion
Last participant's last visit for all outcomes
May 15, 2027
September 15, 2026
September 1, 2026
1 month
September 6, 2026
September 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Healthy Lifestyle Behaviours in Pregnancy Scale
Description: Change in healthy lifestyle behaviours during pregnancy, measured using the Healthy Lifestyle Behaviours in Pregnancy Scale, a 29-item, 5-point Likert-type scale with a total score ranging from 29 to 145. Higher scores indicate more positive healthy lifestyle behaviours during pregnancy.
Baseline (8-12 weeks of gestation), post-intervention (20 weeks of gestation), and follow-up (32 weeks of gestation).
Pregnancy Related Empowerment Scale
Description: Change in empowerment levels among pregnant women, measured using the Pregnancy-Related Empowerment Scale, a 13-item, 4-point Likert-type scale with a total score ranging from 13 to 52. Higher scores indicate higher levels of empowerment among pregnant women.
Baseline (8-12 weeks of gestation), post-intervention (20 weeks of gestation), and follow-up (32 weeks of gestation).
Quality of Life in Pregnancy Scale (PREG-QOL)
Description: Change in quality of life among pregnant women, measured using the Quality of Life in Pregnancy Scale (PREG-QOL), a 26-item scale with a total score ranging from 26 to 130. Thirteen items are reverse-scored. Higher scores indicate better quality of life among pregnant women.
Baseline (8-12 weeks of gestation), post-intervention (20 weeks of gestation), and follow-up (32 weeks of gestation).
Study Arms (2)
Podcast-Supported Prenatal Education Group
EXPERIMENTALParticipants assigned to this group will receive an online prenatal education program based on the Health Promotion Model for four weeks. The program will consist of eight educational modules delivered twice weekly. Following each session, a podcast related to the educational content will be provided. Reminders and motivational messages will be sent during the intervention period to encourage podcast listening and continued participation.
Control Group
NO INTERVENTIONParticipants assigned to the control group will not receive the study intervention during the intervention period.
Interventions
The intervention is a four-week online prenatal education program based on the Health Promotion Model. The program consists of eight educational modules delivered twice weekly. Each session provides structured prenatal education addressing health-promoting behaviors during pregnancy. Following each online education session, participants receive a podcast related to the session content to reinforce the educational messages and support learning outside the scheduled sessions. During the four-week intervention period, reminders to listen to the podcasts and motivational messages are sent to encourage continued participation and engagement with the program.
Eligibility Criteria
You may qualify if:
- Are pregnant women aged 18-35 years;
- Have not been diagnosed with a high-risk pregnancy;
- Have no hearing or visual impairment that would interfere with participation in the intervention;
- Are able to speak and understand Turkish;
- Have access to the internet; and
- Use a smartphone or tablet.
You may not qualify if:
- Are already participating in prenatal education at the hospital's pregnancy school;
- Do not complete the entire educational program;
- Are identified as having a maternal or fetal risk during the intervention period; or
- Indicate a desire to withdraw from the study at any stage.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Tokat Gaziosmanpasa Universitylead
- Hacettepe Universitycollaborator
Study Sites (2)
Tokat Gaziosmanpasa University
Tokat Province, Tokat Province, 60500, Turkey (Türkiye)
Hacettepe University
Ankara, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This is an open-label study. Participants, care providers, and investigators are not masked to group allocation. However, the statistical analysis will be performed by an independent data analyst who will be blinded to the identity of the intervention and control groups through coded group labels.
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer
Study Record Dates
First Submitted
September 6, 2026
First Posted
September 11, 2026
Study Start (Estimated)
December 15, 2026
Primary Completion (Estimated)
January 15, 2027
Study Completion (Estimated)
May 15, 2027
Last Updated
September 15, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared with other researchers because the data contain potentially identifiable and sensitive participant information. Data will be used only for the purposes specified in the study protocol and will be securely stored and managed in accordance with applicable ethical and data protection requirements.