Effectiveness of Metaverse-Based Immersive Technology Intervention for Oral Health Education: A Quasi-Experimental Study

August 3, 2024 updated by: Amirul Faiz bin Luai, Universiti Teknologi Mara
To evaluate the effectiveness of pre- and post-intervention of oral health education using three interventions (conventional methods, mHealth, and the Metaverse platform) on the oral health status, knowledge, practices, and attitudes among secondary school students in Malaysia.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Background: In the last couple of years, the reach of the Internet is leading the world into a unique virtual dimension. Immersive technologies such as virtual reality (VR), augmented reality (AR), mixed reality (MR), extended reality (XR), and metaverse offer diverse virtual experiences and are gaining attention for their supportive role in addressing general health and oral health concerns. Dwivedi et al., in 2022, discussed and set out the potential research agenda in the metaverse in education and health. The metaverse environment offers users an immersive component and experience compared to the traditional environment . According to Locurcio, oral health education and promotion can be provided virtually to target groups and communities through public or private health sector metaverse software for public benefits. Due to no additional cost or limitation in the number of participants, it can educate multiple target groups by providing different sessions from anywhere in the world. These can benefit schoolchildren, teachers, and caregivers. Due to the immersive and interactive nature, the creation of safe and controlled environments and adaptation to the learners' characteristics, immersive technologies and metaverse specifically can facilitate and increase the inclusion of students in educational activities. Hence, the metaverse in oral health promotion and education can revolutionise how people learn, practise, and maintain good oral health. It can also make oral health information more accessible, engaging, and practical, ultimately leading to a positive behavioural change in oral health. Currently, virtual oral health education is often delivered through online platforms like social media, Zoom, Google Meet, and Microsoft Teams. In the future, individually customised oral health education will likely utilise more natural-feeling and immersive platforms, such as the metaverse. The development of metaverse platforms is intricate and context-specific and necessitates input from various relevant stakeholders. Few studies on creating health promotion applications have demonstrated that youth have distinct preferences for digital interventions compared to adults.

Aim: To evaluate the effectiveness of pre- and post-intervention of oral health education using three interventions (conventional methods, mHealth, and the Metaverse platform) on the oral health status, knowledge, practices, and attitudes among secondary school students in Malaysia.

Participants: Secondary school students from identified semi-government school in Malaysia.

Study risk: Participation to this study will not possess any potential risk, and the risk is minimal. Partcipants are free to decline to answer any of the questions that they feel uncomfortable with.

Benefits of the study: There may or may not be any benefits to the participants.

The study involves 15-16 years old adolescents enrolling in a semi-government school in Malaysia which will be divided into three groups that receive three interventions simultaneously at the same time and place (conventional methods, mHealth, and the Metaverse platform)

Duration of the study: Expected to be within six (months) from 1/05/2024 - 31/12/2024

Funding: This research received no external funding.

Conflicts of Interest: The authors declare no conflict of interest.

Ethical Policy and Review Board Statement: The study was approved by the UiTM Faculty of Dentistry Research Ethics Committee (FRC) [REC/07/2023 (PG/MR/228)]. Permission was granted from the Majlis Amanah Rakyat to use Maktab Rendah Sains MARA (MRSM) schools as study sites [MARA.600-6/1/6 JLD2 (56)].

Study Type

Interventional

Enrollment (Estimated)

210

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Malaysia
    • Pahang
      • Bentong, Pahang, Malaysia, 28700
        • Recruiting
        • Maktab Rendah Sains MARA Bentong, MRSM Bentong
        • Contact:
    • Selangor
      • Sungai Buloh, Selangor, Malaysia, 47000
        • Active, not recruiting
        • Faculty of Dentistry, Universiti Teknologi MARA

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. aged 15-16 years old in 2024
  2. voluntarily wish to participate in the research with consent from their legal guardians
  3. enrolled in a co-education school (providing education to both boys and girls)
  4. willing to commit to the program
  5. can understand both Malay and English
  6. participating schools must possess the necessary computer facilities to facilitate this aspect of the study

Exclusion Criteria:

  1. aged less or more than 15-16 years old in 2024
  2. not voluntarily wish to participate in the research with consent from their legal guardians
  3. not enrolled in a co-education school (providing education to both boys and girls)
  4. not willing to commit to the program
  5. can't understand both Malay and English
  6. participating schools does not possess the necessary computer facilities to facilitate this aspect of the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Conventional oral health education
For the conventional oral health education, the trained and calibrated dentist will provide health education to the selected participants in this group by chalk and talk method, PowerPoint presentations, models and charts so that it can make the sessions more interactive. The duration of the session will be around 60-90 minutes. Pre-assessment will be taken prior to the lecture. Post assessment will be taken after the lecture to assess the oral health knowledge, practise and attitude.
Other: Oral health education lecture
Conventional oral health education will be given by trained and calibrated dentists.
Experimental: Oral health education via mHealth using WhatsApp
For the oral health education intervention via mHealth, WhatsApp medium will be used to disseminate oral health educational material. Before the commencement of the study, the participants will be asked for their phone number in the respondent sheet and permission will be sought from both participants and their teachers and parents/guardians. Then, a WhatsApp group will be created consisting of the selected participants for this intervention. The participants in WhatsApp group will further receive WhatsApp instant messages. These participants will grouped and placed in class. These messages will be sent in both Malay and English language. The duration of the session will be around 60-90 minutes. Pre-assessment will be taken prior to the dissemination of oral health education on WhatsApp. Post assessment will be taken afterwards to assess the oral health knowledge, practise and attitude.
Other: Oral health education via mHealth on WhatsaApp
For the oral health education intervention via mHealth, WhatsApp medium will be used to disseminate oral health educational material
Experimental: Metaverse platform called Metaverse for Oral Health Education (Meta-OHE)
For oral health education intervention via Meta-OHE, it will be done via computer in a computer lab. The participants will be gathered in their school's computer lab with the health of the teacher. Participants will be assigned a computer to each of them. Then, they will be asked to sign in into Mitoworld platform using their respective email address on https://mitoworld.io/world/w/2808/meta-ohe to access Meta-OHE. They will be asked to enter the Meta-OHE portal. The students are permitted to freely explore and follow the instruction to visit each section of the Meta OHE and interact with each other. They will also be assigned a few tasks for them to complete on the platform to ensure all the oral health education materials are being covered. The duration of the session will be around 60-90 minutes. Pre-assessment will be taken prior to their access to Meta-OHE. Post assessment will be taken afterwards to assess the oral health knowledge, practise and attitude.
Other: Oral health education via Metaverse platform on Meta-OHE
For oral health education intervention via Meta-OHE, it will be done via computer.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Oral health knowledge
Time Frame: Pre-intervention (baseline) and immediately after the intervention
Level of oral health knowledge. Descriptive, association and correlation
Pre-intervention (baseline) and immediately after the intervention
Oral health practise
Time Frame: Pre-intervention (baseline) and immediately after the intervention
Level of oral health practise. Descriptive, association and correlation
Pre-intervention (baseline) and immediately after the intervention
Oral health attitude
Time Frame: Pre-intervention (baseline) and immediately after the intervention
Level of oral health attitude. Descriptive, association and correlation
Pre-intervention (baseline) and immediately after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Universiti Teknologi Mara

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

August 1, 2024

Primary Completion (Estimated)

December 31, 2024

Study Completion (Estimated)

May 31, 2025

Study Registration Dates

First Submitted

July 26, 2024

First Submitted That Met QC Criteria

August 3, 2024

First Posted (Actual)

August 7, 2024

Study Record Updates

Last Update Posted (Actual)

August 7, 2024

Last Update Submitted That Met QC Criteria

August 3, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • REC/07/2023 (PG/MR/228)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All the information obtained in this study ARE STRICTLY CONFIDENTIAL will be kept and handled in a confidential manner, in accordance with applicable laws and/or regulations. When publishing or presenting the study results, the participants' identity will not be revealed without your expressed consent. Individuals involved in this study, qualified monitors and auditors, and governmental or regulatory authorities may inspect the study data, where appropriate and necessary. All the data will be kept in a password protected folder that only can be access by the researcher. To obtain such information, a formal email need to be sent to the researcher at amirulfaiz2308@gmail.com (personal email) or 2022622294@student.uitm.edu.my (university email). Stored in non-publicly available repository, Available on request, Published as a supplement to the results publication

IPD Sharing Time Frame

2 years

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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