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A Just-in-Time Digital Learning Platform for Teacher Oral Health Training

8 giugno 2026 aggiornato da: Arshed Muhammad, Universiti Putra Malaysia

A Just-in-Time Digital Learning Platform for Teacher Oral Health Training: Effects on Oral Health Literacy, Implementation, and Student Oral Health Outcomes in a Randomized Controlled Trial

This randomized controlled trial aims to evaluate the effectiveness and implementation of a Just-in-Time Digital Learning Platform designed to improve teachers' oral health literacy and support the delivery of oral health education in schools. Teachers play an important role in promoting healthy behaviors among children, but many have limited access to structured oral health training. Digital microlearning approaches may provide a scalable and cost-effective solution for strengthening teacher capacity in school-based oral health promotion.

Teachers assigned to the intervention group will receive access to a digital learning platform that delivers short, interactive, and evidence-based oral health training modules through mobile devices. The platform will provide educational content, reminders, quizzes, feedback, and progress monitoring. Teachers in the control group will receive standard information or routine training practices.

The study will assess changes in teachers' oral health literacy, knowledge, attitudes, and confidence in delivering oral health education. It will also evaluate implementation outcomes, including acceptability, feasibility, adoption, fidelity, reach, and engagement with the digital platform. In addition, the study will examine whether improvements in teacher training lead to better oral health knowledge, behaviors, and clinical oral health outcomes among students.

Panoramica dello studio

Descrizione dettagliata

Oral diseases remain among the most prevalent chronic conditions affecting children worldwide and disproportionately burden populations in low- and middle-income countries. Schools are recognized as an important setting for oral health promotion because they provide sustained access to children during critical periods of behavioral development. Teachers are key agents in implementing school-based oral health interventions; however, limited training opportunities, competing responsibilities, and resource constraints often reduce their effectiveness in delivering oral health education.

Digital learning technologies provide opportunities to overcome these challenges through flexible, scalable, and low-cost training approaches. Just-in-Time learning is an educational strategy that delivers concise information at the point of need, enabling users to acquire knowledge and skills in a timely and accessible manner. Despite growing interest in digital health education, evidence regarding the effectiveness and implementation of digital oral health training for teachers remains limited.

This randomized controlled trial will evaluate a Just-in-Time Digital Learning Platform developed to improve teachers' oral health literacy and strengthen the delivery of school-based oral health promotion activities. The intervention consists of short digital microlearning modules, interactive quizzes, reminders, feedback mechanisms, and performance-monitoring features accessible through mobile devices.

The primary objective is to determine the effect of the intervention on teachers' oral health literacy. Secondary objectives include assessing changes in teachers' oral health knowledge, attitudes, self-efficacy, and educational practices, as well as student oral health knowledge, behaviors, and clinical oral health outcomes. The study will further evaluate implementation outcomes including acceptability, feasibility, adoption, fidelity, reach, engagement, and sustainability using implementation science frameworks. Equity analyses will assess whether intervention effects differ according to school location, socioeconomic characteristics, or other contextual factors.

The results will contribute to the evidence base for digital capacity-building strategies in school health programs and provide guidance for policymakers seeking scalable and sustainable approaches to improve oral health promotion through educational systems.

Tipo di studio

Interventistico

Iscrizione (Stimato)

870

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Sindh
      • Karachi, Sindh, Pakistan, 74600
        • Saleem ullah fahmi school baqai Medical complex gharo
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria: Teachers aged ≥18 years. Currently employed in participating schools. Access to a smartphone, tablet, or computer with internet connectivity. Able to understand the intervention language. Willing to provide informed consent and participate in study activities. -

Exclusion Criteria: Currently participating in another oral health training program or research study.

Planning to leave employment at the participating school during the study period.

Unable to access or use the digital learning platform. Refusal or withdrawal of informed consent.

-

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Ricerca sui servizi sanitari
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Just-in-Time Digital Learning Platform for Teacher Oral Health Training
Participants in this arm will receive access to a Just-in-Time Digital Learning Platform designed to improve teachers' oral health literacy and capacity to deliver school-based oral health education. The intervention includes short mobile-based microlearning modules, educational videos, interactive quizzes, reminders, feedback, digital learning resources, and progress tracking. Content covers oral health knowledge, preventive practices, oral hygiene promotion, and classroom implementation strategies. Teachers will engage with the platform throughout the intervention period and apply learned concepts in routine school activities. The intervention is designed to improve teacher oral health literacy, implementation outcomes, and student oral health outcomes.
Teachers assigned to the intervention group will receive access to a mobile-based Just-in-Time Digital Learning Platform delivering short oral health microlearning modules, interactive quizzes, reminders, educational resources, and feedback. The intervention aims to improve teachers' oral health literacy, teaching practices, and implementation of school-based oral health promotion activities, ultimately improving student oral health outcomes.
Nessun intervento: Standard Teacher Training or Routine Practice
Participants in this arm will continue routine educational practices and receive standard training or information available through existing school systems. They will not receive access to the Just-in-Time Digital Learning Platform during the study period. Outcomes will be assessed at the same time points as the intervention group.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Teacher Oral Health Literacy Score
Lasso di tempo: Baseline to post-intervention (e.g., 6 months)
Teacher oral health literacy will be assessed using a structured oral health literacy questionnaire completed by participating teachers at baseline and post-intervention. Each item will be scored according to the questionnaire scoring instructions, and item scores will be summed to generate a total oral health literacy score. Higher scores will indicate greater oral health literacy. The primary analysis will compare the change in mean oral health literacy score from baseline to post-intervention between the intervention and control groups.
Baseline to post-intervention (e.g., 6 months)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Teacher oral health knowledge
Lasso di tempo: 6 Months
Structured 20-30 item MCQ questionnaire on caries, plaque, brushing, fluoride, diet, referral, and prevention
6 Months
Teaching self-efficacy
Lasso di tempo: 6 Months
8-10 Likert-scale items assessing confidence to teach oral health, demonstrate brushing, answer questions, and refer children
6 Months
AIM score
Lasso di tempo: 6 Months
Acceptability of Intervention Measure, 4 items
6 Months
IAM score
Lasso di tempo: 6 Months
Intervention Appropriateness Measure, 4 items
6 Months
FIM score
Lasso di tempo: 6 Months
Feasibility of Intervention Measure, 4 items
6 Months
Training completion rate
Lasso di tempo: 6 Months
Digital platform analytics: number of completed modules divided by total assigned modules
6 Months
Fidelity
Lasso di tempo: 6 Months
Classroom observation checklist assessing whether teachers delivered key oral health messages and activities as planned
6 Months
Student oral health knowledge
Lasso di tempo: 6 Months
Age-appropriate 10-20 item questionnaire on brushing, sugar intake, dental visits, and tooth protection
6 Months
Student oral health behaviour
Lasso di tempo: 6 Months
Self-reported questionnaire on brushing frequency, fluoride toothpaste use, sugary snack intake, and dental care-seeking
6 Months
OHI-S
Lasso di tempo: 6 Months
Clinical oral examination using Greene and Vermillion Simplified Oral Hygiene Index
6 Months
Plaque Index
Lasso di tempo: 6 Months
Silness and Löe Plaque Index assessed on selected teeth/surfaces
6 Months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Muhammad Arshed, PhD, Baqai Medical University

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

15 giugno 2026

Completamento primario (Stimato)

24 ottobre 2026

Completamento dello studio (Stimato)

30 ottobre 2026

Date di iscrizione allo studio

Primo inviato

8 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

8 giugno 2026

Primo Inserito (Effettivo)

12 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

8 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • BMUU

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

The study protocol, statistical plan, and results will be disseminated through publications in peer-reviewed Journals.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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