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Recruiting NCT05938166

The Effects of Using Augmented Reality (AR) System to Train Foreign Care Workers.

No phase Interventional Oral Dryness and Saliva Altered Oral Manifestations Swallowing Disorder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: oral care augmented reality (AR), video-based oral hygiene education course.
Who it may be relevant to
Registry conditions: Oral Dryness and Saliva Altered, Oral Manifestations, Swallowing Disorder. Basic parameters: 21 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effects of Using Augmented Reality (AR) System to Train Foreign Care on Salivary Biomarker and Oral Function of the Elderly People

Overview

The aim of this study was to evaluate the effect of augmented reality (AR) system training intervention of foreign care workers on the salivary biomarker and oral function of older people. This randomized controlled trial included experimental group: AR group (EG-A) Video group (EG-B) and control group(CG), respectively. The EG-A will receive augmented reality (AR) system training intervention with AR tooth-cleaning skills session course add video-based oral hygiene education course . The EG-B receive video-based oral hygiene education course and The CG only receive only a leaflet.

Detailed description

A randomized experimental design was used. Female foreign care workers whose aged 21 to 65 years and by cared older peoples whose aged 65 to 75 years were recruited through community-based site of long-term care service in Kaohsiung city. Each group was expected for 12 care workers and by cared older peoples who each group. G\*Power (version 3.1.9.4) was used for power analysis.

All foreign care workers whose participants will underwent questionnaire examination at baseline and at 1-month, 3-month, 6-month follow-ups. The information of foreign care workers regarding oral care cognition, attitude, self-efficacy, and oral care behavior intention will be collected by a self-report questionnaire before and after intervention.

Each by cared older peoples will be evaluation oral hygiene and function by oral hygienist, and will completed the questionnaire at baseline and at 1-month, 3-month and 6-month follow-up. Older people by cared will assess plaque control record (PCR), tongue coating index (TCI), repetitive saliva swallowing test (RSST), oral diadochokinetic (DDK), oral moisture degree (OMD),masticatory efficiency (MoE) and salivary biomarker at baseline (Time 1), three months (Time 2) and six months (Time 3) follow-ups.

Interventions

  • Device oral care augmented reality (AR)
    Augmented reality (AR) is an extension of perceptible reality, whereby additional information, such as texts or virtual objects, can be displayed in the user's field of vision.The oral care augmented reality (AR) simulation training can train foreign care workers by switching languages (Indonesian) and therefore reduce language-related learning barriers.
  • Other video-based oral hygiene education course
    50-minute video-based oral hygiene education course

Primary outcome measures

  • Tongue Coating Index(TCI) [Time frame: Change from Baseline TCI at 1-month after intervention]
  • Tongue Coating Index(TCI) [Time frame: Change from Baseline TCI at 3-month after intervention]
  • Tongue Coating Index(TCI) [Time frame: Change from Baseline TCI at 6-month after intervention]
  • Oral Dryness Status [Time frame: Change from Baseline Oral Dryness Status at 1-month after intervention]
  • Oral Dryness Status [Time frame: Change from Baseline Oral Dryness Status at 3-month after intervention]
  • Oral Dryness Status [Time frame: Change from Baseline Oral Dryness Status at 6-month after intervention]
  • Lip-Tongue Motor Function [Time frame: Change from Baseline lip-tongue motor function Status at 1-month after intervention]
  • Lip-Tongue Motor Function [Time frame: Change from Baseline lip-tongue motor function Status at 3-month after intervention]
  • Lip-Tongue Motor Function [Time frame: Change from Baseline lip-tongue motor function Status at 6-month after intervention]
  • Maximum tongue pressure (MTP) [Time frame: Change from Baseline Maximum tongue pressure status at 1-month after intervention]
Secondary outcome measures (3)
  • GOHAI-T(Geriatric Oral Health Assessment Index-Taiwan) [Time frame: Change from Baseline at 1 month after intervention]
  • GOHAI-T(Geriatric Oral Health Assessment Index-Taiwan) [Time frame: Change from Baseline at 3 month after intervention]
  • GOHAI-T(Geriatric Oral Health Assessment Index-Taiwan) [Time frame: Change from Baseline at 6 month after intervention]

Eligibility criteria

Inclusion criteria

  • 1\. The Indonesian caregivers who are employed in Kaohsiung City are aged between 21 and 65 and have simple Chinese communication skills.
  • 2\. The elderly people being cared for is over 65 years old.

Exclusion criteria

  • 1\. Elderly people who are unable to cooperate with instructions.
  • 2\. Elderly people with facial impairment.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Supportive care

Study locations

Taiwan · 1 center
  • Kaohsiung Medical University — Kaohsiung City

Publications

  • Chang AH, Lin PC, Lin PC, Lin YC, Kabasawa Y, Lin CY, Huang HL. Effectiveness of Virtual Reality-Based Training on Oral Healthcare for Disabled Elderly Persons: A Randomized Controlled Trial. J Pers Med. 2022 Feb 4;12(2):218. doi: 10.3390/jpm12020218. PMID 35207706

Identifiers

NCT: NCT05938166 · KMUHIRB-SV(II)-20230019

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗