ClinicalTrials.gg
Not yet recruitingNCT07645612Updated Jun 12, 2026

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

An interventional study of Just-in-Time Digital Learning Platform for Teacher Oral Health Training in Oral Health Behavior Change, Oral Hygiene, Oral Health and Digital Literacy, sponsored by Universiti Putra Malaysia. Not yet recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-12.

Sponsored by Universiti Putra Malaysia · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
870
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Oral Health Behavior Change
  • Oral Hygiene, Oral Health
  • Digital Literacy

Keywords

  • Oral Health Literacy; Digital Learning; Teacher Training; Implementation Outcomes; Health Equity
03

In context

Health Behavior

967 studies on the registry are indexed under Health Behavior; 165 are open to participants now.

This study's planned enrollment of 870 is above the median of 150 across 824 interventional studies indexed under Health Behavior.

Browse Health Behavior studies →

Lead sponsor

Universiti Putra Malaysia is the lead sponsor of 145 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

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 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.

-

Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Care provider, Investigator, Outcomes assessor)
Enrollment
870 participants (estimated)

Study arms

  • Experimental
    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.

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

  • No intervention
    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.

Interventions

  • BehavioralJust-in-Time Digital Learning Platform for Teacher Oral Health Training

    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.

06

What researchers measure

Primary outcomes

  1. Teacher Oral Health Literacy Score

    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.

    Time frame: Baseline to post-intervention (e.g., 6 months)

Secondary outcomes

  1. Teacher oral health knowledge

    Structured 20-30 item MCQ questionnaire on caries, plaque, brushing, fluoride, diet, referral, and prevention

    Time frame: 6 Months

  2. Teaching self-efficacy

    8-10 Likert-scale items assessing confidence to teach oral health, demonstrate brushing, answer questions, and refer children

    Time frame: 6 Months

  3. AIM score

    Acceptability of Intervention Measure, 4 items

    Time frame: 6 Months

  4. IAM score

    Intervention Appropriateness Measure, 4 items

    Time frame: 6 Months

  5. FIM score

    Feasibility of Intervention Measure, 4 items

    Time frame: 6 Months

  6. Training completion rate

    Digital platform analytics: number of completed modules divided by total assigned modules

    Time frame: 6 Months

  7. Fidelity

    Classroom observation checklist assessing whether teachers delivered key oral health messages and activities as planned

    Time frame: 6 Months

  8. Student oral health knowledge

    Age-appropriate 10-20 item questionnaire on brushing, sugar intake, dental visits, and tooth protection

    Time frame: 6 Months

  9. Student oral health behaviour

    Self-reported questionnaire on brushing frequency, fluoride toothpaste use, sugary snack intake, and dental care-seeking

    Time frame: 6 Months

  10. OHI-S

    Clinical oral examination using Greene and Vermillion Simplified Oral Hygiene Index

    Time frame: 6 Months

  11. Plaque Index

    Silness and Löe Plaque Index assessed on selected teeth/surfaces

    Time frame: 6 Months

07

Study locations

1 site
08

References and documents

Publications

  • Weiner BJ, Lewis CC, Stanick C, Powell BJ, Dorsey CN, Clary AS, Boynton MH, Halko H. Psychometric assessment of three newly developed implementation outcome measures. Implement Sci. 2017 Aug 29;12(1):108. doi: 10.1186/s13012-017-0635-3. PubMed 28851459 ↗
  • Kameg BN, Constantino RE. #MeToo and "Time's Up": Implications for Psychiatric and Mental Health Nurses. J Am Psychiatr Nurses Assoc. 2018 May/Jun;24(3):188-189. doi: 10.1177/1078390318763267. No abstract available. PubMed 29779463 ↗
  • Maus T, Carter R, El-Yahchouchi C, Geske J, Diehn F. Letter to the editor. Pain Med. 2014 May;15(5):879-81. doi: 10.1111/pme.12425. Epub 2014 Mar 21. No abstract available. PubMed 24655572 ↗
  • De Gagne JC, Park HK, Hall K, Woodward A, Yamane S, Kim SS. Microlearning in Health Professions Education: Scoping Review. JMIR Med Educ. 2019 Jul 23;5(2):e13997. doi: 10.2196/13997. PubMed 31339105 ↗

Individual participant data

Plan to share: No — The study protocol, statistical plan, and results will be disseminated through publications in peer-reviewed Journals.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07645612
Responsible party
Arshed Muhammad (Principal Investigator, Universiti Putra Malaysia) — Principal investigator
First posted
Jun 12, 2026
Start date
Jun 15, 2026 (estimated)
Primary completion
Oct 24, 2026 (estimated)
Completion
Oct 30, 2026 (estimated)
Last update
Jun 12, 2026

Study contacts

Muhammad Arshed, Ph.D.
Contact
drarshedchaudhary@gmail.com
+923337474464
Muhammad Arshed, PhD
principal investigator · Baqai Medical University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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