Peking Union Medical College Hospital Dementia Study Tracking Cognitive Impairment in Older Adults in China
Led by Peking Union Medical College Hospital · Updated on 2022-09-13
20000
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Researchers are conducting a hospital-based observational study called the PUMCH Dementia Cohort, focusing on elderly Chinese individuals with cognitive impairment. The study aims to address the growing burden of dementia in China by exploring risk and prognostic factors, disease characteristics, cognitive assessments, biomarkers, diagnosis, and treatment of dementia and its subtypes. This effort seeks to build a comprehensive dementia database to improve clinical diagnosis, treatment, and prevention strategies.
The study collects detailed baseline information including demographics, clinical history, physical exams, and extensive neuropsychological testing covering screening and specific cognitive domains. Biological samples like serum, cerebrospinal fluid, urine, skin, and saliva are stored for biomarker analysis. Participants are grouped by age at dementia onset and controls with normal cognition are included. Follow-up occurs every six months, with brain autopsy samples collected upon death to verify biomarkers and disease characterization.
Participants provide data through regular clinical visits, cognitive tests, behavioral assessments, and collection of various fluid and tissue samples. The study tracks the incidence of dementia, cognitive and functional decline, neuropsychiatric symptoms, and biomarker changes over an average of 10 to 20 years. Education and training on dementia, as well as development of computer-assisted diagnostic and evaluation systems using machine learning, are also part of the study. The total participation duration varies as it is a long-term observational cohort.
CONDITIONS
Brief Title
PUMCH Dementia Longitudinal Cohort Study
Research Team
C
Chenhui Mao, Doctor
J
Jing Gao, Doctor
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Diagnosis of neurodegenerative dementia based on 2011 NIA-AA criteria
Having a fixed caregiver who can help with regular follow-up visits
You will not qualify if you...
Not diagnosed with dementia, including mild cognitive impairment (MCI)
Having severe systemic diseases or serious vision or hearing problems that affect follow-up or neuropsychological evaluation
Lacking a fixed caregiver
Refusal to provide informed consent
Expected life expectancy shorter than 2 years
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Long-term Monitoring
Duration - Up to 20 years
Participants undergo regular evaluations including cognitive tests, behavioral assessments, and biomarker sample collections to monitor dementia progression and related risk factors.
Visits every 6 months
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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Published Research Related To This Trial
Multidomain lifestyle intervention benefits a large elderly population at risk for cognitive decline and dementia regardless of baseline characteristics: The FINGER trial.