NeuroCare Community Project: Early Alzheimer's Detection in Hong Kong
Official title: NeuroCare Community Project: A Community Based Prospective Observational Study for Early Alzheimer's Detection in Hong Kong
Run by Hong Kong University of Science and Technology · NCT07347574 · Data updated 2026-11-12
This study tests whether blood and brain imaging biomarkers, along with clinical assessments, can identify normal aging, mild cognitive impairment, and Alzheimer's disease in a Hong Kong community.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 60 Years to 75 Years |
| Sex | All |
| Enrollment | 2500 (estimated) |
| Sponsor | Hong Kong University of Science and Technology Academic / other |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | March 23, 2026 |
| Main results expected | December 30, 2030 |
| Study ends | December 30, 2030 |
| Registry record updated | July 8, 2026 |
| Trial ID | NCT07347574 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are community-dwelling adults in Hong Kong who are mentally capable of consent and willing to undergo blood draws and study assessments.
✕Probably not a fit
Individuals who are unwilling or unable to provide blood samples, undergo assessments, or participate in follow-up may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, community-based observational cohort study in Hong Kong aimed at identifying biomarkers and imaging patterns that distinguish clinically normal individuals, MCI, and AD. It will compare clinical assessments, diagnoses, and blood biomarker panels against MRI and PET imaging as reference standards. The study plans to pre-screen about 6,000 elderly individuals and enroll around 2,500 participants for cross-sectional analysis, with 2–3 years of longitudinal follow-up over a 5-year period. The project will explore novel blood and imaging markers for AD diagnosis and progression, with data collection spanning clinical, cognitive, biomarker, and neuroimaging metrics.
Why it matters
Potential benefit: If successful, the project could improve early detection and tracking of AD in the community, enabling timely care planning.
How similar studies have gone: Previous studies in other populations have shown that combining biomarkers with imaging can improve early detection of AD, but this project focuses on an ethnic Chinese population in a community setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Mentally capable of providing informed consent, with or without an informant present * Willing and able to undergo blood draw and complete study related assessments; willing to be contacted for follow-up Exclusion Criteria: * Lacks capacity to consent even with an informant present * Refuses or is unable to provide blood samples or complete essential assessments * Currently enrolled in another clinical trial that could interfere with this study * Known illness that prevents longitudinal follow up or uncontrolled medical illness such as neurodevelopmental disorder, neurodegenerative disease, epilepsy, central nervous system infection, neuroinflammatory diseases, brain tumor, cerebrovascular diseases, history of major psychiatric illness, history of major head injury with altered consciousness, sexually transmitted disease including HIV and syphilis, visual and auditory disability, history of alcohol dependence, substance use disorder, systemic autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis, or malignancy. * Active delirium or evidence of reversible/secondary causes of cognitive impairment (e.g., vitamin B12 deficiency, hypothyroidism) until treated/ stabilized
Where it's running
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Hong Kong University of Science and Technology
Hong Kong, China Recruiting
Study contacts
- Principal investigator: Nancy Ip, PhD — Hong Kong University of Science and Technology
- Study coordinator: Nancy Ip, PhD
- Email: boip@ust.hk
- Phone: +852-23587304
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.