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Use of an AI-powered Mobile Health App in Assessing and Training Oral Motor Functions (ORAR SG)

2026年11月6日 更新者:The Hong Kong Polytechnic University

This project aims to evaluate the usability of the ORAR app developed by HKPU and normed on the Hong Kong Chinese population, with the Singapore Malay and Chinese population.

It aims to:

  1. Establish normative data of the oromotor performance of neurologically healthy bilinguals of Malay ethnicity and/or Chinese ethnicity across a range of speech and non-speech tasks.
  2. Determine the factors (e.g., gender, age, education, type of stimuli, ethnicity) that influence oro-motor performance of Malay and Chinese adults respectively in Singapore.
  3. Collect feedback to evaluate the usability, acceptability and feasibility of the ORAR app from different users, namely the SLTs, persons with dysarthria and their caregivers.

研究概览

研究类型

观察性的

注册 (估计的)

405

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

21年 至 79年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

概率样本

研究人群

The study aims to recruit 150 Singaporean Malay bilinguals and 150 Singaporean Chinese bilinguals. These participants will comprise a range of ages (21-79 years old), with 25 participants from each decade age group.

描述

Inclusion Criteria for healthy adults:

  • (1) Adults aged 21-79 years who are Singapore citizens
  • (2) Absence of severe systemic conditions, including uncontrolled diabetes, cerebrovascular disease, head and neck tumours, or neurological disorders
  • (3) Not currently undergoing radiation therapy or chemotherapy
  • (4) Normal or corrected-to-normal vision and hearing
  • (5) Fluent in Malay/ English respectively
  • (6) No history of speech difficulties/disorders

Inclusion criteria for participants with dysarthria:

  • (1) Adults aged 21-79 years who are Singapore citizens
  • (2) Absence of severe systemic conditions, including uncontrolled diabetes, cerebrovascular disease, head and neck tumours, or neurological disorders
  • (3) Not currently undergoing radiation therapy or chemotherapy
  • (4) Normal or corrected-to-normal vision and hearing
  • (5) Fluent in Malay/ English respectively

Additional inclusion criteria for SLTs:

  • (1) AHPC licensed
  • (2) have been practising in Singapore for at least one year

Exclusion Criteria:

  • (1) individuals who are dependent on non-oral feeding
  • (2) individuals unable to provide informed consent due to cognitive impairment

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:OTHER
  • 时间观点:PROSPECTIVE

队列和干预

团体/队列
干预/治疗
healthy adults

For the normative study: 150 individuals of Malay descent (e.g., Boyanese, Javanese, Banjarese, Bugis, and Indonesian extract) and 150 bilingual Chinese individuals. Another 35 speech-language therapists and carers of dysarthric pateints will be recruited.

Inclusion criteria for healthy adults in the normative study, as well as SLTs and caregivers of individuals with dysarthria in the implementation study are as follows: (1) Adults aged 21-79 years who are Singapore citizens, (2)absence of severe systemic conditions, including uncontrolled diabetes, cerebrovascular disease, head and neck tumours, or neurological disorders, (3) not currently undergoing radiation therapy or chemotherapy, (4) normal or corrected-to-normal vision and hearing, (5) fluent in Malay/ English respectively, (6) no history of speech difficulties/disorders. Additional inclusion criteria for SLTs are: (1) AHPC licensed and (2) have been practising in Singapore for at least one year.

Dysarthria group

35 individuals with neurogenic dysarthria will be recruited. For the implementation study, inclusion criteria for participants with dysarthria include (1) to (5) above, with the exception of a history of stroke, and being diagnosed with an acquired speech sound disorder by an SLT. Exclusion criteria include (1) individuals who are dependent on non-oral feeding, (2) individuals unable to provide informed consent due to cognitive impairment. Written or digital consent will be obtained from all participants prior to participation.

Feasibility Study:

Participants wi l first complete a demographic form that collects information such as age, occupation, gender, housing type, and dental history.

This study will be conducted in a controlled environment, such as a quiet room at SIT, clinics, and participants' homes, under the guidance of SLT students. Participants wi l complete three 4-item measures of implementation outcomes - Acceptability of Intervention Measure (AIM), Intervention Appropriateness Measure (IAM), and Feasibility of Intervention Measure (FIM; Weiner et al., 2017). Subsequently, they will be given 30 minutes to explore and experiment with the app's different features. Following this, participants will complete the AIM, IAM, and FIM again, as well as participate in a semi-structured interview with the SLT student on their experience using the app and feedback about the app. The app wil be available in Mandarin (Simplified) and English.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Range of movement of the articulators
大体时间:2-hr assessment

The range of movement of lips, tongue, and jaw of the participants will be analyzed by the computer vision model of ORAR to give range-of-motion scores.

2-hr assessment
Maximum phonation time
大体时间:2-hr assessment

Each participant will be asked to take a deep breathe and say 'ah' as long as they can. This will repeat for 3 times.

2-hr assessment
Diadochokinetic (DDK) rate
大体时间:2-hr assessment

The number of repeated syllables, trisyllabic non-word, trisyllabic Malay real word (only for Malay participants), trisyllabic English real word produced in 8 seconds will be measured.

2-hr assessment
Reading aloud a word list
大体时间:2-hr assessment

Participants will be asked to read aloud a word list covering phonetic inventory of the language and multisyllabic words (English: 38 words from Robertson Dysarthria Profile; Malay: 30 words selected from Malay Lexicon Project).

2-hr assessment
Personal narrative production
大体时间:2-hr assessment

Participants will be asked to recall a personal event.

2-hr assessment
Verbal fluency tasks
大体时间:2-hr assessment

Participants will be asked to produce as many items in a given category (e.g., fruits, vehicles) within a minute.

2-hr assessment
Acceptability, appropriateness and feasibility of ORAR
大体时间:2-hr assessment

A semi-structured interview will be conducted. Questions regarding the acceptability, apropriateness and feasibility of ORAR app will be asked.

2-hr assessment

次要结果测量

结果测量
措施说明
大体时间
Eating Assessment Tool (EAT-10) questionnaire as a self-reported outcome instrument on swallowing functions
大体时间:2-hr assessment

The questionnaire consists of 10 questions, and participants will be asked to evaluate their swallowing functions based on a 5-point Likert scale (0=not at all; 4=very much). Lower scores reflect better swallowing performance. Maximum and minimal scores are 40 and 0, respectively.

2-hr assessment
The Oral Health Impact Profile-14 (OHIP-14) questionnaire to assess oral health-related quality of life
大体时间:2-hr assessment

Participants will be asked to give ratings on the questionnaire based on a 5-point Likert scale. Lower scores represent better oral condition-related quality of life. The maximum and minimum scores are 56 and 0, respectively.

2-hr assessment

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年2月1日

初级完成 (估计的)

2028年8月31日

研究完成 (估计的)

2028年8月31日

研究注册日期

首次提交

2026年11月6日

首先提交符合 QC 标准的

2026年11月6日

首次发布 (实际的)

2026年11月12日

研究记录更新

最后更新发布 (实际的)

2026年11月12日

上次提交的符合 QC 标准的更新

2026年11月6日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

The IPD, together with the study protocol, will be shared in an open-access data repository (e.g., OSF).

IPD 共享时间框架

Data will be shared starting from three months after manuscript publication.

IPD 共享访问标准

The IPD and study protocol will be shared in an open-access data repository without restrictions.

IPD 共享支持信息类型

  • 研究方案
  • 国际碳纤维联合会

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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