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UnknownNCT03275363

The University of Hong Kong Neurocognitive Disorder Cohort

Status
Unknown
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
The University of Hong Kong · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Accepted

Summary

The HKU Neurocognitive Disorder (NCD) Cohort is a hospital-based, prospective, observational study of older HK Chinese adults with cognitive impairment, with a special focus on studying patients with subjective cognitive decline and mild cognitive impairment.

Detailed description

The HKU Neurocognitive Disorder (NCD) Cohort is a hospital-based, prospective, observational study of older HK Chinese adults with cognitive impairment, with a special focus on studying patients with subjective cognitive decline and mild cognitive impairment, and in particular the biomarkers that predict cognitive and functional decline. Comprehensive profiling of each subject is performed through a multi-domain assessment protocol including detailed demographics, lifestyle factors, neuropsychological battery, mood, MRI, genetics, blood biomarkers, and other patient-centred parameters including level of disability, quality of life and societal engagement. Ongoing annual follow up captures the essential clinical events and changes in neurocognitive function (conversion to MCI or dementia), mood, level of disability and quality of life; as well as repeat blood tests. The HKU NCD Cohort is the first-ever Asian dementia cohort to be formally included into the Dementia Platforms UK, achieving an international collaborative status with other UK-based cohorts. The study neuropsychological battery is aligned with the NACC UDS3 battery.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTNeurocognitive batteryCognitive impairment status (SCD, MCI, dementia), HK-MoCA, Clinical Dementia Rating (CDR sum of squares), Geriatric Depression Scale (GDS-15), Neuropsychiatric Index (NPI), Barthel Index, Lawton's IADL, Life-Space Assessment, Mini-Nutrition Assessment (MNA), Quality of Life for Alzheimer's Disease (QoL-AD, patient and carer parts), frailty status (FRAIL scale), handgrip strength, walking speed, exercise status, sleep quality, Charlson comorbidity index (CCI, age-adjusted). NACC: Story recall, Benson's complex figure copy, colour trail test (black \& white), verbal fluency, digit forward and backward span.
DIAGNOSTIC_TESTMRIMRI: T1, T2, FLAIR, SWI, DTI, fMRI, ASL, MRS, for selected patients
BIOLOGICALBlood testsStored samples (unanalysed): serum, plasma, buffy coat (PBMC); also processed for microvesicles and exosome analysis
DIAGNOSTIC_TESTEEG with event-related potential (ERP)128-channel EEG with ERP for Go/NoGo and Prospective Memory (PM) tasks for selected patients
DIAGNOSTIC_TESTAmyloid PET CTF18 Flutametamol PET CT for selected patients

Timeline

Start date
2014-09-01
Primary completion
2022-01-01
Completion
2022-01-04
First posted
2017-09-07
Last updated
2017-09-07

Locations

1 site across 1 country: Hong Kong

Source: ClinicalTrials.gov record NCT03275363. Inclusion in this directory is not an endorsement.

The University of Hong Kong Neurocognitive Disorder Cohort (NCT03275363) · Clinical Trials Directory