Actively Recruiting

Age: 50Years +
All Genders
Healthy Volunteers
ID04360200

Cognitive Impairment in Ageing People: A Longitudinal Observational Prospective Study

Led by Yamei Tang · Updated on 2020-09-14

5000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Mild cognitive impairment (MCI) and neurocognitive disorders like Alzheimer's disease and vascular dementia are common among older adults, causing significant medical, social, and economic challenges, especially in China. This research aims to create a long-term observational study to better understand these conditions, focusing on early prevention, diagnosis, and treatment. The study also seeks to identify brain imaging and blood or cerebrospinal fluid markers that could help detect and monitor cognitive disorders early. Participants will be grouped into those experiencing normal aging with normal cognitive function and those with mild cognitive impairment marked by memory loss. The study will build a comprehensive database including epidemiological data, biological samples, and clinical information to track the progression from normal aging to dementia or Alzheimer’s disease. Advanced brain imaging techniques will be used to support precise diagnoses of cognitive disorders. During the study, which runs from April 2020 to December 2040, participants will undergo regular evaluations including cognitive assessments like the Montreal Cognitive Assessment (MoCA). Researchers will monitor the incidence of dementia and the rate at which individuals progress from normal cognition to mild impairment and dementia. Safety and cooperation with procedures such as blood sampling and imaging will be ensured, with ongoing data collection to support early intervention development.

CONDITIONS

Brief Title

Cognitive Impairment in Ageing People

Who Can Participate

Age: 50Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over 50 years old
  • Signed informed consent
  • No diagnosis of dementia according to DSM-IV criteria
  • Clinical dementia rating (CDR) score of 0.5
Not Eligible

You will not qualify if you...

  • Intellectual disability or mental retardation
  • Refusal to undergo blood sampling, imaging, or other examinations
  • Serious organic diseases, history of mental illness, or physical disabilities including severe aphasia
  • Contraindications to MRI scanning
  • Presence of serious physical or mental illness

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.

Long-term Monitoring

Duration - April 2020 to December 2040

Participants are observed over time to monitor cognitive changes and progression toward dementia.

Trial Site Locations

Total: 1 location

1

Sun Yat-sen Memorial Hospital, Sun Yat-sen University

Guangzhou, Guangdong, China, 510120

Actively Recruiting

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Research Team

Y

Yamei Tang

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial