Ireland
--:--IST
Recruiting Observational

Beijing Disability Risk and Ageing Monitoring Study

NCT06394817 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2023-02-20
Last updated
2024-06-20

Condition(s) studied

Age ProblemDisabilityDeath

Investigational drug(s) / intervention(s)

No intervention

No intervention: No intervention

Study summary

This is a community-based prospective cohort study in Beijing, China. The study has been initialized in 2023 and enrolled older residents. This study aims to develop disability risk assessment standards and an early warning model for older adults.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Aged 60 years or older * Lived in the community for more than 1 year * Signed the informed consent form Exclusion Criteria: * Cannot complete the survey

Primary outcome measure(s)

  • The prevalence and incidence of functional disability using a population-based survey — An average of 1 to 2 years
    Functional disability was measured by Activities of Daily Living, cognitive function (Mini-Mental State Examination) and movement disorder(Short Physical Performance Battery) collected by questionnaires.The minimum value of the Activities of Daily Living is 0, and the maximum value is 100, the higher the score, the better the outcome.The minimum value of the Mini-Mental State Examination is 0, and the maximum value is 30, the higher the score, the better the outcome.The minimum value of the Short Physical Performance Battery is 0, and the maximum value is 12, the higher the score, the better the outcome.
  • The prevalence and incidence of mild cognitive impairment using a population-based survey — An average of 1 to 2 years
    Mild cognitive impairment was measured using Mini-Mental State Examination collected by questionnaire.The minimum value of the Mini-Mental State Examination is 0, and the maximum value is 30, the higher the score, the better the outcome.
  • The prevalence and incidence of dementia using a population-based survey — An average of 1 to 2 years
    Dementia was determined by diagnosis of hospitalization or diagnosis of death or Clinical Dementia Rating scale. The minimum value of the Clinical Dementia Rating is 0, and the maximum value is 3, the higher the score, the worse the outcome.
  • The conversion rate of normal to mild cognitive impairment — An average of 1 to 2 years
    Percentage of enrolled population that convert from normal to mild cognitive impairment
  • The conversion rate of mild cognitive impairment to dementia — An average of 1 to 2 years
    Percentage of enrolled population that convert from mild cognitive impairment to dementia
  • The genetic and environmental factors for mild cognitive impairment and dementia at genomic and expression levels — An average of 1 to 2 years
    Discover risk factors including genetic susceptibility loci (APOE genes and other risk genes) using gene sequencing, cardiovascular risk factors (blood glucose, cholesterol, homocysteine) using laboratory tests, and unhealthy lifestyle using questionnaire.
  • The biomarkers for normal, mild cognitive impairment, and dementia diagnosis — An average of 1 to 2 years
    Humoral biomarkers are included Aβ42, Aβ40, phosphated tau and total tau in plasma, cerebrospinal fluid, saliva, and urine. Imaging biomarkers are included cerebral volume, glucose metabolism, amyloid and tau deposition of whole brain or hippocampus.
  • The prevalence and incidence of movement disorder using a population-based survey — An average of 1 to 2 years
    Movement disorder was measured using Short Physical Performance Battery collected by questionnaire.The minimum value of the Short Physical Performance Battery is 0, and the maximum value is 12, the higher the score, the better the outcome.

Trial sites (1)

FacilityCityRegionStatus
Xuanwu Hospital, Capital Medical University Beijing China Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06394817 on ClinicalTrials.gov ↗ ← All trials in China