The University of Hong Kong Neurocognitive Disorder Cohort
- Conditions
- Neurocognitive DisorderVascular DementiaAlzheimer DementiaAge-related Cognitive DeclineMild Cognitive Impairment
- Registration Number
- NCT03275363
- Lead Sponsor
- The University of Hong Kong
- Brief 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.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 500
- Older adults with or without neurocognitive disoder. HKU NCD Cohort focuses primarily on people with Subjective Cognitive Decline (SCD) and Mild Cognitive Impairment (MCI).
- Severe Parkinson's disease, major depressive disorder or severe psychiatric conditions, significant communication difficulties (e.g. aphasia, deafness), terminal cancer or likely end-of-life in the next 12 months.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cognitive decline 1 year Change in total HK-MoCA score between baseline and follow-up
- Secondary Outcome Measures
Name Time Method Functional decline 1 year Change in Lawton's IADL score between baseline and follow-up
Neuropsychiatric decline 1 year Change in Neuropsychiatric Index (NPI) between baseline and follow-up
Quality of life decline 1 year Change in QoL-AD score between baseline and follow-up
Change in cognitive impairment status 1 year Progression to mild cognitive impairment (MCI) or dementia status
Trial Locations
- Locations (1)
Department of Medicine, Queen Mary Hospital, The University of Hong Kong
🇭🇰Hong Kong, Hong Kong
Department of Medicine, Queen Mary Hospital, The University of Hong Kong🇭🇰Hong Kong, Hong KongJoseph SK Kwan, MDContact+85222554769jskkwan@hku.hkCharlene Cheng, BAContact+85222554769cychar@hku.hk