Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID05023564

Peking Union Medical College Hospital Dementia Longitudinal Cohort Study

Led by Peking Union Medical College Hospital · Updated on 2022-09-13

20000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

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

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of neurodegenerative dementia based on 2011 NIA-AA criteria
  • Having a fixed caregiver who can help with regular follow-up visits
Not Eligible

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

Trial Site Locations

Total: 1 location

1

Peking Union Medical College Hospital

Beijing, China

Actively Recruiting

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Research Team

C

Chenhui Mao, Doctor

J

Jing Gao, Doctor

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

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease.

G M McKhann, M S Albert, M Grossman...

https://pubmed.ncbi.nlm.nih.gov/11708987

Multidomain lifestyle intervention benefits a large elderly population at risk for cognitive decline and dementia regardless of baseline characteristics: The FINGER trial.

Anna Rosenberg, Tiia Ngandu, Minna Rusanen...

https://pubmed.ncbi.nlm.nih.gov/29055814