CClinicalTrials.gg
Active, not recruitingNCT05479318Updated Feb 15, 2024

A Global Approach to Tackle Cognitive Decline

An observational study in Dementia, sponsored by Chinese University of Hong Kong. Active, not recruiting at 1 site in Hong Kong. Open to participants aged 60 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-02-15.

Sponsored by Chinese University of Hong Kong · Observational

From the registry’s dates

  • Primary completion was expected by May 2025, 1 year 5 months ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
1,502
Ages
60 Years and older
Sex
All
01

Study summary

The number of people suffering from dementia in Asia (22.9 million) is more than twice the numbers in Europe (10.5 million) or the Americas (9.4 million), as recorded in the global impact of dementia in the World Alzheimer Report 2015.1 This dementia tsunami will continue to rise and the estimated number is 67 million in 2050 in Asia alone, which will be 2 to 3 times higher than the estimates for Europe (19 million) or the Americas (30 million). Devising and implementing preventive strategies against dementia is of paramount importance. The proposed project will be able to establish the associations between VRFs and cognition across cohorts with cultural, ethnical, and demographical variations. This study will generate data for evidence-based knowledge for globally implementable and effective preventive strategies for cognitive impairment and dementia.

Read the detailed description

Participants will be retrospectively selected from a Hong Kong Chinese cohort, a Singaporean cohort, a British cohort, two European cohorts, and an Australian cohort.

Subjects from the above listed cohorts who fit the study criteria will be selected for this study.

Demographical information, clinical, vascular risk factors, MRI images and cognitive data will be retrieved from the cohorts.

02

Conditions studied

  • Dementia
03

In context

Cognitive Dysfunction

3,843 studies on the registry are indexed under Cognitive Dysfunction; 1,100 are open to participants now.

This study's enrollment of 1,502 is above the median of 150 across 950 observational studies indexed under Cognitive Dysfunction.

Browse Cognitive Dysfunction studies →

Lead sponsor

Chinese University of Hong Kong is the lead sponsor of 1,419 studies on the registry; 487 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Subjects will be retrospectively selected from 7 cohorts from Hong Kong, Australia, Singapore and Europe areas.

Inclusion criteria

  1. Elderly community-dwelling individuals aged over 60 years old;
  2. those with at least 2 time points of detailed cognitive measurements, with 2-3 years of assessment interval;
  3. with at least 1 timepoint of MRI (T1, FLAIR, and DTI).

Exclusion criteria

Exclusion Criteria:

  1. subjects with stroke, dementia, and other neurological diseases at baseline;
  2. those without longitudinal cognitive data;
  3. those without MRI data available.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
1,502 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Record of any vascular risk factors

    medical history of hypertension, diabetes mellitus, hyperlipidemia, smoking and drinking, record unit as yes or no

    Time frame: Baseline

  2. Record of triglyceride level

    triglyceride level, as one of vascular risk factors, unit as mmol/L

    Time frame: Baseline

  3. Record of high-density-lipoprotein level,

    high-density-lipoprotein level, as one of the vascular risk factors, unit as mmol/L

    Time frame: Baseline

  4. Record of low-density-lipoprotein level,

    low-density-lipoprotein level, as one of the vascular risk factors, unit as mmol/L

    Time frame: Baseline

  5. Record of total cholesterol level,

    total cholesterol level, as one of the vascular risk factors, unit as mmol/L

    Time frame: Baseline

  6. Record of glycated hemoglobin

    glycated hemoglobin, as one of the vascular risk factors, unit as percentage

    Time frame: Baseline

  7. Record of fasting blood glucose

    fasting blood glucose from blood results, as one of vascular risk factors, unit as mmol/L

    Time frame: Baseline

  8. Record of blood pressure

    Blood pressure, as one of vascular risk factors, unit as mmHg

    Time frame: Baseline

  9. Record of pulse

    Pulse rate, as one of vascular risk factors, unit as bpm

    Time frame: Baseline

  10. Change of Mini-Mental State Examination

    Mini-Mental State Examination is used for measuring general cognition including the domains of attention and processing speed, executive function, memory, visuospatial function, and animal fluency.

    Time frame: Baseline and 3rd year follow up

  11. Change of Montreal Cognitive Assessment

    Montreal Cognitive Assessment is used for measuring general cognition including the domains of attention and processing speed, executive function, memory, visuospatial function, and animal fluency.

    Time frame: Baseline, 1 yr, 2yr and 3rd year follow ups

  12. Changes of brain white matter abnormalities

    brain white matter abnormalities can be observed through the FLAIR sequence of brain MRI images

    Time frame: Baseline and 1 yr, 2yr and 3rd year follow ups

07

Study locations

1 site
  • Prince of Wales Hospital
    Shatin, N.t. 00000, Hong Kong
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 15, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05479318
Lead sponsor
Chinese University of Hong Kong
Collaborators
The University of New South Wales, University of Oxford, University College, London, Umeå University, Max Planck Institute for Human Development, National University of Singapore
Responsible party
Bonnie Yin Ka LAM (Research Assistant Professor, Chinese University of Hong Kong) — Principal investigator
First posted
Jul 29, 2022
Start date
Sep 1, 2022
Primary completion
May 1, 2025 (estimated)
Completion
Oct 1, 2025 (estimated)
Last update
Feb 15, 2024

Study contacts

Bonnie Yin Ka Lam
principal investigator · Chinese University of Hong Kong

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

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