Actively Recruiting

Age: 65Years +
All Genders
Healthy Volunteers
NCT06863727

The Beijing Longitudinal Disability Survey in Community Elderly

Led by Xuanwu Hospital, Beijing · Updated on 2025-03-07

1962

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

Sponsors

X

Xuanwu Hospital, Beijing

Lead Sponsor

B

Beijing Municipal Health Commission

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this observational study is to establish the prospective cohort of the Beijing Longitudinal Disability Survey in Community Elderly (BLINDSCE) to explore the high-risk factors and preventive interventions for disability and cognitive impairment among community-dwelling adults aged 65 years and over. The main question it aims to answer is: * What are the high-risk factors able to predict the incidence and advance of disability and cognitive impairment in community-dwelling adults aged 65 years and over? * What are the categories of function and cognitive performance trajectory in community-dwelling adults aged 65 years and over?

CONDITIONS

Official Title

The Beijing Longitudinal Disability Survey in Community Elderly

Who Can Participate

Age: 65Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Community-dwelling adults aged 65 years or older who reside in Beijing.
  • Participants who sign an institutionally approved informed consent.
Not Eligible

You will not qualify if you...

  • Participants with severe mental disorders and serious medical conditions preventing study investigation.
  • Participants undergoing long-term professional treatment for physical function and cognitive functioning, such as hospitalization or rehabilitation.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Xuanwu Hospital, Capital Medical University

Beijing, China, 100053

Actively Recruiting

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Research Team

Y

Yansu Guo, Ph.D

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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