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Reminder-based Educational Mobile Intervention for for Maternal Oral Health Literacy and Preschoolers' Dental Health (REMIND)

16 de agosto de 2026 actualizado por: Pani Matin Anugrah

The Effectiveness of a Notification- and Reminder-Based Educational Application in Improving Maternal Oral Health Literacy and the Dental Health Status of Preschool Children in Pancoran Mas

The goal of this clinical trial is to determine the effectiveness of educational application based on notification and reminder in improving maternal oral health literacy and the dental and dental health status of preschool children among mother-preschool child pairs (children aged <7 years) in Pancoran Mas, Depok City.

The primary research questions to be addressed in the main trial are:

  • Does the application group improve mothers' oral health literacy (measured using the REALD-30 questionnaire) more than the printed booklet group?
  • Does the application group improve children's oral health status, as measured by oral hygiene (Debris Index-Simplified [DI-S]) and gingival condition (modified Gingival Index [mGI]), more than the printed booklet group?
  • What is the level of usability (ease of use) of the application as perceived by mothers who use it?

The researchers will compare a group of mothers who receive education through the application with a group of mothers who receive education through a printed booklet to determine whether the application produces greater improvements in maternal oral health literacy and children's oral health outcomes.

Participants will be asked to:

  • Complete the REALD-30 questionnaire at baseline (pretest) and at the end of the program (posttest), with a one-month interval between assessments.
  • Accompany their children for DI-S and mGI examinations at baseline (pretest) and at the end of the program (posttest), with a one-month interval between assessments, conducted by a calibrated dentist.
  • Receive and study dental health education materials delivered progressively, one chapter per week, through either the application (intervention group) or a printed booklet (control group). Subsequent chapters will be unlocked in the following week.
  • Complete a daily checklist documenting their child's tooth-brushing activities every morning and evening throughout the study period.
  • For participants in the application group only: receive daily notifications/reminders and personalized educational messages (based on quiz scores and checklist compliance levels), and complete the Mobile App Usability Questionnaire (MAUQ) at the end of the program.

Descripción general del estudio

Descripción detallada

Study Design and Setting:

This study employed a quasi-experimental design with a pretest-posttest non-equivalent control group approach and was conducted in parallel between the intervention and control groups in seven preschool in Pancoran Mas , Depok City, Indonesia, between July and December 2024. Participant allocation was non-randomized. The sample size was calculated using the analytical formula for comparing numerical between two independent groups. The final sample size was determined to be 100 participants in each group, yielding a total analytical sample of 200 mother-child pairs. Participants were recruited through a non-probability purposive sampling method at the village and school levels.

Intervention:

The study compared two educational media containing identical content on tooth anatomy, oral hygiene practices, oral diseases, and the development of dental caries (four chapters):

  • Application (Peri Bugi): An interactive mHealth application featuring daily notifications and reminders, supplemented with a rule-based AI system that personalizes the frequency of educational messages according to quiz performance and compliance with the toothbrushing checklist.
  • Booklet: A printed text-based educational material designed for self-directed learning.

Study Protocol:

  1. Application Development. The development process included conceptual planning (objectives, target users, framework, and REALD-30-based content), UI/UX wireframe design, development of the four educational chapters, and prototype creation.
  2. Expert Evaluation. Four experts (two computer science experts and two experts/master's students in community dentistry) evaluated the feasibility and usability of the prototype online via Zoom using the System Usability Scale (SUS) questionnaire. The evaluation results were used to revise and improve the application.
  3. Pilot Study. Twenty end users (10 in the application group and 10 in the booklet group) tested the intervention over a two-week period. Baseline assessments included the REALD-30 questionnaire for mothers and the Oral Hygiene Index-Simplified (OHI-S) for children.
  4. Main Effectiveness Trial

    • Baseline Assessment: All participants completed a pretest to assess baseline conditions. Mothers completed the REALD-30 questionnaire, while children underwent DI-S and mGI examinations performed by calibrated dentists.
    • Intervention Period: Participants in the intervention group used the Peri Bugi application, whereas those in the control group used the printed booklet. Educational materials were delivered progressively, with one chapter released each week over a four-week period. Participants were also required to complete morning and evening toothbrushing checklists. Coordination regarding chapter release schedules was conducted through WhatsApp groups.
    • Post-Intervention Assessment: One month after baseline, all participants completed a posttest involving the same assessments administered at baseline. In addition, participants in the intervention group completed an application usability assessment.

Assessment Tools:

Oral Health Literacy: The REALD-30 questionnaire (Lee et al., 2007) was used to assess mothers' oral health literacy through recognition of dental terminology. Scores were converted to a 0-100 scale, with higher scores indicating better oral health literacy. The questionnaire was administered at both pretest and posttest.

Children's Oral Health Status: The Debris Index-Simplified (DI-S) was used to assess oral hygiene status, while the Modified Gingival Index (mGI) was used to evaluate gingival health. Both measurements were conducted at pretest and posttest by calibrated dentists.

Application Usability: The Mobile Health App Usability Questionnaire (MAUQ) (Zhou et al., 2019), consisting of three subscales and a 7-point Likert scale, was administered to participants in the intervention group at posttest. Lower scores indicated better usability according to the scoring system applied in this study.

Assessment Tools:

  • Oral Health Literacy: The REALD-30 questionnaire (Lee et al., 2007) was used to assess mothers' oral health literacy through recognition of dental terminology. Scores were converted to a 0-100 scale, with higher scores indicating better oral health literacy. The questionnaire was administered at both pretest and posttest.
  • Children's Oral Health Status: The Debris Index-Simplified (DI-S) was used to assess oral hygiene status, while the Modified Gingival Index (mGI) was used to evaluate gingival health. Both measurements were conducted at pretest and posttest by calibrated dentists.
  • Application Usability: The Mobile Health App Usability Questionnaire (MAUQ) (Zhou et al., 2019), consisting of three subscales and a 7-point Likert scale, was administered to participants in the intervention group at posttest. Higher scores indicated better usability according to the scoring system applied in this study.

Tipo de estudio

Intervencionista

Inscripción (Actual)

200

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.

Ubicaciones de estudio

    • West Java
      • Depok, West Java, Indonesia
        • Seven preschools in Pancoran Mas

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

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Mothers with a child aged 3-7 years (preschool-aged child).
  • Mothers who own a smartphone and are able to download and install applications.
  • Mothers who have internet access and actively use the internet.
  • Mothers who are willing and cooperative to participate in the study from enrollment until study completion.
  • Preschool children aged 3-7 years.
  • Children enrolled in a preschool located in Pancoran Mas, Depok City.

Exclusion Criteria:

  • Mothers who were unwilling to sign the informed consent form.
  • Mothers or children with physical or mental disabilities (e.g., Down syndrome, hearing impairment, visual impairment, cerebral palsy, or other developmental or physical disabilities).
  • Children with congenital diseases or congenital anomalies.
  • Children with systemic diseases, such as congenital heart disease, epilepsy, thalassemia, hemophilia, or other systemic medical conditions.

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: Prevención
  • Asignación: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Intervention Group (Peri Bugi Mobile Application)
Mothers in this group received oral health education through the Peri Bugi mHealth application, a notification- and reminder-based platform equipped with a rule-based AI system that personalized the frequency of educational messages based on quiz scores and compliance with the toothbrushing checklist. Educational materials consisting of four chapters were delivered progressively, with one chapter released each week over a four-week period. In addition, participants received toothbrushing reminder notifications at 6:30 a.m. and 8:00 p.m.
Peri Bugi is an mHealth-based oral health education application developed for Android and iOS devices. The application comprises five main features: Literacy (a four-chapter flipbook containing oral health educational content), Quiz, Toothbrushing Song, Toothbrushing Checklist, and Settings. It provides daily reminder notifications and utilizes a rule-based artificial intelligence (AI) system to personalize dental health education messages based on users' quiz performance and adherence to the toothbrushing checklist.
Comparador activo: Control Group (Printed Booklet)
Mothers in the control group received oral health education through a printed booklet containing content equivalent to that provided in the application. The educational materials, consisting of four chapters, were delivered progressively, with one chapter provided each week over a four-week period for self-directed learning.
A printed text-based oral health education booklet comprising four chapters with content equivalent to that provided in the Peri Bugi application. The booklet was intended for self-directed learning and did not incorporate any notification, reminder, or personalized educational messaging features

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Maternal Oral Health Literacy Score (REALD-30 Questionnaire)
Periodo de tiempo: Baseline (pretest) and 1 month post-intervention (posttest)
Change in mothers' oral health literacy, measured using the Rapid Estimation of Adult Literacy in Dentistry (REALD-30) questionnaire. Scores range from 0 to 30, with each correctly recognized dental term scored as 1 and each incorrectly recognized term scored as 0. Higher scores indicate better oral health literacy. Changes in scores are assessed by comparing pretest and posttest measurements.
Baseline (pretest) and 1 month post-intervention (posttest)
Children's Oral Hygiene Status (DI-S)
Periodo de tiempo: Baseline (pretest) and 1 month post-intervention (posttest)
Change in the oral hygiene status of preschool children, measured using the Debris Index-Simplified (DI-S) based on the extent of soft debris present on the surfaces of index teeth (score range: 0-3 per tooth surface). Lower scores indicate better oral hygiene. Examinations are performed by calibrated dentists. Changes are assessed by comparing pretest and posttest measurements.
Baseline (pretest) and 1 month post-intervention (posttest)
Children's Gingival Health Status (m-GI)
Periodo de tiempo: Baseline (pretest) and 1 month post-intervention (posttest)
Change in the gingival health status of preschool children, measured using the Modified Gingival Index (mGI) based on the severity of gingival inflammation. Lower scores indicate healthier gingival conditions. Examinations are conducted by calibrated dentists. Changes are assessed by comparing pretest and posttest measurements.
Baseline (pretest) and 1 month post-intervention (posttest)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Application Usability Score (MAUQ)
Periodo de tiempo: 1 month post-intervention (posttest)
Mothers' perceptions of the usefulness and ease of use of the Peri Bugi application, measured using the Mobile Health App Usability Questionnaire (MAUQ). The MAUQ consists of three subscales: ease of use and satisfaction, system information arrangement, and efficiency, using a 7-point Likert scale. Lower scores indicate better usability according to the scoring system used in this study. This outcome is assessed only among participants in the intervention group.
1 month post-intervention (posttest)

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Investigador principal: Risqa Rina Darwita, Prof., Indonesia University

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

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 (Actual)

15 de julio de 2024

Finalización primaria (Actual)

3 de diciembre de 2024

Finalización del estudio (Actual)

9 de diciembre de 2024

Fechas de registro del estudio

Enviado por primera vez

16 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

16 de agosto de 2026

Publicado por primera vez (Actual)

19 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

19 de agosto de 2026

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

16 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 61/Ethical Approval/FKGUI/IX/2
  • PKS 149/UN2.RST/HKP.05.00/2025 (Otro número de subvención/financiamiento: Universitas Indonesia PUTI Q1 Equity Grant 2025)

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 made publicly available in order to maintain the confidentiality and privacy of participants (mothers and preschool-aged children), in accordance with the requirements of the ethics approval.

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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