Fact CheckerSign in

NCT03946930Recruiting

Cognitive Decline in AD

A Cohort Study of Cognitive Decline in Alzheimer Disease

Source: ClinicalTrials.gov · Last updated 21 Aug 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

There is lack of information on the risk factors of accelerated cognitive decline in older people with Alzheimer disease (AD). The extent of neurodegeneration and white matter disease has been reported to be important factors. In addition there may be biomarkers e.g. inflammatory cytokines that can contribute to cognitive decline. The impact of care arrangement and physical activity may also be important. Insulin signaling is impaired in Alzheimer disease (AD). We therefore propose to perform a cohort study of older people with AD. This will be based on an on-going AD registry which was designed to identify genetic biomarkers for AD. Detailed neurocognitive tests and lifestyle information are available. In addition, volumetric MRI brain scans were performed in all AD subjects. The hypothesis is that MRI brain volumes, serum biomarkers, physical activity, physical functioning are independently associated with cognitive decline in older people with AD. The objective is to identify risk factors of accelerated cognitive decline so that preventive measures can be designed to delay dependency in AD.

Status (registry)
Recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
8 May 2019
Start date
13 Dec 2018
Primary completion date
31 Dec 2027
Lead sponsor
Chinese University of Hong Kong
NCT number
NCT03946930

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 13 Dec 2018 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Subjects who refuse blood taking procedure
  • No reliable family caregiver informant (person contact at least once a month)

Who the study is looking for

  • Sufficient Cantonese competency for cognitive test
  • Clinical diagnosis of AD
  • FAST test staging 3-5

Age in the registry: 65 years to 92 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Chinese University of Hong Kong
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.