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Clinical Trials/NCT05479318
NCT05479318Active, not recruitingNot Applicable

A Global Approach to Tackle Cognitive Decline

Chinese University of Hong Kong1 site in 1 country1,502 target enrollmentStarted: September 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
1,502
Locations
1
Primary Endpoint
Record of any vascular risk factors

Study Overview

Brief 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.

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
60 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

Record of any vascular risk factors

Time Frame: Baseline

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

Record of low-density-lipoprotein level,

Time Frame: Baseline

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

Record of total cholesterol level,

Time Frame: Baseline

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

Record of pulse

Time Frame: Baseline

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

Record of triglyceride level

Time Frame: Baseline

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

Record of high-density-lipoprotein level,

Time Frame: Baseline

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

Record of fasting blood glucose

Time Frame: Baseline

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

Record of glycated hemoglobin

Time Frame: Baseline

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

Change of Montreal Cognitive Assessment

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

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.

Changes of brain white matter abnormalities

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

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

Record of blood pressure

Time Frame: Baseline

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

Change of Mini-Mental State Examination

Time Frame: Baseline and 3rd year follow up

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Bonnie Yin Ka LAM

Research Assistant Professor

Chinese University of Hong Kong

Study Sites (1)

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