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cMIND AI Web Tool Usability Study (Hong Kong)

2026年7月24日 更新者:Hong Kong Metropolitan University

Development and Validation of a Web-Based AI System for Assessing the Cantonese-Style Mediterranean Diet (cMIND) Index

This study is testing a new web-based tool that uses artificial intelligence (AI) to help older adults in Hong Kong check how healthy their Cantonese-style meals are for brain health. The tool is based on the cMIND diet, a Chinese-adapted version of a known healthy eating pattern that may support memory and thinking skills.

Participants will use the web app to take photos of their usual meals for at least 10 days over two weeks. The AI will automatically identify ingredients and give a score showing how well the meal follows the cMIND diet. The study will also ask participants to complete a short questionnaire and a brief interview to find out how easy and useful the tool is for older adults.

The purpose of this small study is to see whether the AI tool is user-friendly and acceptable for older people. Results will help improve the tool for future use to support healthy ageing and brain health.

調査の概要

詳細な説明

Mild cognitive impairment (MCI) is common among older adults and can progress to dementia. Diet plays an important role in brain health. The cMIND diet is a culturally adapted Chinese version of the Mediterranean-DASH diet, designed to support cognitive function. However, many older adults find it difficult to track their adherence to this diet using traditional methods.

This study is developing and testing a simple web-based AI tool to help older adults in Hong Kong monitor their Cantonese-style meals. Users take photos of their meals (such as dim sum, stir-fries, or congee) using the web app. The AI automatically identifies ingredients in mixed dishes and calculates a cMIND adherence score (0-12), giving immediate personalised feedback on how well the meal supports brain health.

The main part of the study is a small usability and acceptability test. We will recruit 20 community-dwelling older adults aged 60 years and above who regularly eat Cantonese-style meals. Participants should not have a self-reported diagnosis of dementia or Alzheimer's disease, or other psychiatric/medical conditions that would interfere with participation or valid outcome assessment.

Eligible participants will receive a 20-minute training session on how to use the web tool. They will then use the app to photograph their usual meals for at least 10 days over a two-week period, without changing their normal eating habits.

At the end of the two weeks, participants will complete a short online questionnaire about the ease of use and usefulness of the tool. They will also take part in one short individual interview (about 20 minutes, audio-recorded) to share their experiences and suggestions.

This low-risk study aims to understand whether older adults find the AI tool easy and acceptable to use in daily life. The results will help improve the prototype for future larger studies. All data will be kept strictly confidential, and ethics approval has been obtained from the Hong Kong Metropolitan University Research Ethics Committee (Reference: HE-FRSE/2026/08).

研究の種類

観察的

入学 (推定)

20

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

サンプリング方法

非確率サンプル

調査対象母集団

Community-dwelling older adults aged 60 years and above in Hong Kong who regularly consume Cantonese-style meals.

説明

Inclusion Criteria:

  • Aged 60 years or above
  • Community-dwelling in Hong Kong
  • Able to provide informed consent
  • Basic ability to use a smartphone or tablet (with assistance if needed)
  • Consuming Cantonese-style meals as the primary dietary pattern for ≥ 5 days per week for the past 3 months or longer)

Exclusion Criteria:

  • Severe visual or motor impairment that prevents taking meal photos even with assistance
  • Self-reported diagnosis of dementia or Alzheimer's disease, or other psychiatric/medical conditions that would interfere with participation or valid outcome assessment
  • Current participation in other interventional nutrition or technology studies

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
介入・治療
cMIND Usability Group
Community-dwelling older adults aged 60 years and above in Hong Kong who regularly consume Cantonese-style meals. This single-group feasibility and usability study evaluates the ease of use and acceptability of a web-based AI tool that analyses meal photos and calculates a cMIND (Cantonese-style Mediterranean Diet) adherence score to support cognitive health monitoring.
A web-based AI software prototype designed specifically for older adults in Hong Kong. Users upload photographs of their usual Cantonese-style mixed meals (e.g., dim sum assortments, stir-fries with overlapping ingredients, or congee with toppings). The AI system automatically recognises multiple ingredients and sauces, estimates nutritional content using local food composition data, and calculates a cMIND adherence score (range 0-12). Immediate personalised feedback on dietary quality for brain health is provided. The tool is intended for dietary self-monitoring and does not involve any drug, physical device, or medical treatment.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Usability and Acceptability of the Web-Based AI Tool
時間枠:Assessed at the end of the 2-week testing period
Participants' perceived ease of use and acceptability of the AI web tool for photographing Cantonese meals and receiving cMIND dietary feedback.
Assessed at the end of the 2-week testing period

二次結果の測定

結果測定
メジャーの説明
時間枠
Feasibility of Meal Photo-Taking
時間枠:Over the 2-week testing period
Proportion of participants able to complete at least 10 days of meal photos over the two-week period.
Over the 2-week testing period
Qualitative User Feedback
時間枠:At the end of the 2-week testing period
Participants' experiences, challenges, and suggestions regarding the web tool, collected through semi-structured interviews.
At the end of the 2-week testing period

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Chow Ka-Man, Ph.D.、Hong Kong Metropolitan University

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2027年9月1日

一次修了 (推定)

2028年1月1日

研究の完了 (推定)

2028年2月1日

試験登録日

最初に提出

2026年7月24日

QC基準を満たした最初の提出物

2026年7月24日

最初の投稿 (実際)

2026年7月29日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月29日

QC基準を満たした最後の更新が送信されました

2026年7月24日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

De-identified individual participant data (including meal photos, cMIND scores, and usability questionnaire responses) will be made available upon reasonable request after publication of the main results. A data dictionary will be provided.

IPD 共有時間枠

Start Date: 6 months after publication of the main study results End Date: 5 years after study completion (January 2033)

IPD 共有アクセス基準

IPD and supporting documents (study protocol, informed consent form, and data dictionary) will be made available to qualified researchers upon reasonable request for the purpose of academic research or meta-analysis. Requests should be directed to the Principal Investigator (Dr. Ariel Chow Ka Man) via email.

A formal data sharing agreement will be required. The agreement will specify the purpose of data use, data security requirements, and prohibition of re-identification of participants. Requests will be reviewed by the Principal Investigator and co-investigators to ensure scientific merit and compliance with ethics requirements. Data will be provided in de-identified format.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • ICF

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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