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Podcast-Supported Prenatal Education Based on the Health Promotion Model (PPE-HPM)

10 de septiembre de 2026 actualizado por: Abdurrahim UYANIK, Tokat Gaziosmanpasa University

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

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.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Descripción detallada

Pregnancy is an important period in which women experience substantial physical, psychological, and social changes that may influence their health behaviors, sense of empowerment, and quality of life. Prenatal education can support pregnant women in developing healthy lifestyle behaviors, making informed health-related decisions, and adapting to the changes associated with pregnancy. However, conventional prenatal education may be limited by time, accessibility, and the ability of women to review educational content at their own pace.

The Health Promotion Model provides a theoretical framework for understanding and supporting health-promoting behaviors by addressing individual characteristics, perceived benefits and barriers, self-efficacy, interpersonal influences, and situational factors. Integrating this model into prenatal education may help pregnant women recognize factors affecting their health behaviors and strengthen their ability to actively participate in decisions related to their health during pregnancy.

Podcasts may provide an accessible and flexible method for reinforcing prenatal education. Because podcast content can be listened to repeatedly and at a time and place convenient for the participant, it may facilitate continued engagement with educational information beyond scheduled online sessions. Combining structured online prenatal education with podcast-based reinforcement may therefore provide an innovative approach to supporting health promotion during pregnancy.

This study is designed to determine whether a prenatal education program based on the Health Promotion Model and supported by podcasts can improve pregnant women's empowerment, healthy lifestyle behaviors, and quality of life compared with routine prenatal care. The intervention is intended to provide structured educational content while reinforcing key messages through podcasts, reminders, and motivational communication throughout the intervention period.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

60

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • 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.

Exclusion Criteria:

  • 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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Investigación de servicios de salud
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Podcast-Supported Prenatal Education Group
Participants 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.
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.
Sin intervención: Control Group
Participants assigned to the control group will not receive the study intervention during the intervention period.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Healthy Lifestyle Behaviours in Pregnancy Scale
Periodo de tiempo: Baseline (8-12 weeks of gestation), post-intervention (20 weeks of gestation), and follow-up (32 weeks of gestation).
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
Periodo de tiempo: Baseline (8-12 weeks of gestation), post-intervention (20 weeks of gestation), and follow-up (32 weeks of gestation).
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)
Periodo de tiempo: Baseline (8-12 weeks of gestation), post-intervention (20 weeks of gestation), and follow-up (32 weeks of gestation).
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).

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

15 de diciembre de 2026

Finalización primaria (Estimado)

15 de enero de 2027

Finalización del estudio (Estimado)

15 de mayo de 2027

Fechas de registro del estudio

Enviado por primera vez

6 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

6 de septiembre de 2026

Publicado por primera vez (Actual)

11 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

15 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

10 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • Hacettepe University PhD

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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