NCT07735013

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
5mo left

Started Sep 2027

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 24, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 29, 2026

Completed
1.1 years until next milestone

Study Start

First participant enrolled

September 1, 2027

Expected
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2028

1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2028

Last Updated

July 29, 2026

Status Verified

July 1, 2026

Enrollment Period

4 months

First QC Date

July 24, 2026

Last Update Submit

July 24, 2026

Conditions

Keywords

cMIND dietCantonese Mediterranean dietAI dietary assessmentweb-based AI toolmeal photo analysisCantonese mixed dishesusability testingolder adultscongitive healthmild cognitive impairmenthealthy ageinggerontechnologynutrition monitoringdietary adherenceAI food recognitionCantonese cuisinebrain health dietfeasibility studyacceptability studyHong Kong older adults

Outcome Measures

Primary Outcomes (1)

  • Usability and Acceptability of the Web-Based AI Tool

    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

Secondary Outcomes (2)

  • Feasibility of Meal Photo-Taking

    Over the 2-week testing period

  • Qualitative User Feedback

    At the end of the 2-week testing period

Study Arms (1)

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.

Other: Web-Based AI Dietary Assessment System

Interventions

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.

cMIND Usability Group

Eligibility Criteria

Age60 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

  • 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)

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Cognitive Dysfunction

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental Disorders

Study Officials

  • Chow Ka-Man, Ph.D.

    Hong Kong Metropolitan University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Chow Ka-Man, Ph.D.

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 24, 2026

First Posted

July 29, 2026

Study Start (Estimated)

September 1, 2027

Primary Completion (Estimated)

January 1, 2028

Study Completion (Estimated)

February 1, 2028

Last Updated

July 29, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will share

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.

Shared Documents
STUDY PROTOCOL, ICF
Time Frame
Start Date: 6 months after publication of the main study results End Date: 5 years after study completion (January 2033)
Access Criteria
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.