Comprehensive Assessment of Neurodegeneration and Dementia

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50-90
SponsorMcGill University

About this trial

This is a longitudinal observational study recruiting individuals between the ages of 50 and 90 with different types of dementia as well as a comparison group without cognitive deficits. Participants are/will be recruited at sites across Canada and will undergo assessments, neuroimaging, and biological sample collection.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Has subjective or objective cognitive impairment

Written informed consent must be obtained and documented (from the patient or, where jurisdictions allow it, from a caregiver/family member)

Sufficient proficiency in English or French to undertake self report and neuropsychological testing

Geographic accessibility to the study site

Disqualifiers

The presence of other significant known chronic brain disease such as: moderate to severe chronic static leukoencephalopathy (including previous traumatic injury), multiple sclerosis, a serious developmental handicap, malignant tumors, Parkinson's disease (other than for the Parkinson's cohort), and other rarer brain illnesses

Ongoing alcohol or drug abuse which in the opinion of the investigator may interfere with the subject's ability to comply with the study procedures

Symptomatic stroke within the previous year

Unable to undergo MRI scan due to medical contraindications or inability to tolerate the procedure

Trial population

2300 English and/or French-speaking participants recruited from across Canada in the following groups: * 650 Cognitively healthy volunteers * 300 volunteers with Subjective Cognitive Decline * 400 volunteers with Mild Cognitive Impairment * 200 volunteers with Vascular Mild Cognitive Impairment * 150 volunteers with Alzheimer's disease * 200 volunteers with Dementia of Mixed Etiology * 200 volunteers with Parkinson's disease and cognitive impairment * 200 volunteers with Frontotemporal spectrum dementia

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,573 Participants
are grouped into 8 trial groups

8

Trial groups

See each trial group below.

Group A: Normal healthy elderly
Group B: Subjective Cognitive Decline
Group C: Mild Cognitive Impairment (MCI)
Group D: Vascular MCI
Group E: Alzheimer's Disease
Group F: Dementia of Mixed Etiology
Group G: Lewy Body/Parkinson's spectrum
Group H: Frontotemporal dementia (FTD) spectrum

Trial outcomes

Primary outcomes

1

Montreal Cognitive Assessment (MoCA) score

change in MoCA total score. The MoCA is a test of global cognition scored out of 30 with a higher score indicating better performance. The minimum score is 0 and the maximum score is 30.

Time frame
8 years

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

McGill University

Lead sponsor

Baycrest

Sponsor institution

Canadian Institutes of Health Research (CIHR)

Collaborator

Alzheimer Society of Canada

Collaborator

Sanofi

Collaborator

New Brunswick Health Research Foundation

Collaborator

Saskatchewan Health Research Foundation

Collaborator

Michael Smith Foundation for Health Research

Collaborator

Nova Scotia Health Research Foundation

Collaborator

Eli Lilly and Company

Collaborator

Canadian Nurses Foundation (CNF)

Collaborator

Ontario Brain Institute

Collaborator

Pfizer

Collaborator

Canadian Consortium on Neurodegeneration in Aging

Collaborator