Improving Prognostic Confidence in Neurodegenerative Diseases Causing Dementia Using Peripheral Biomarkers and Integrative Modeling

Status: Recruiting
Location: See all (4) locations...
Study Type: Observational
SUMMARY

To develop a model to predict disease progression in a large cohort of patients across a variety of neurodegenerative diseases, including Mild Cognitive Impairment (MCI) and dementia due to any neurodegenerative disease, including Alzheimer's Disease (AD), Lewy Body Disease (LBD), Vascular Disease (VaD) and Frontotemporal lobar degeneration (FTLD).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 95
Healthy Volunteers: f
View:

• Referring diagnosis of MCI or early dementia

• Age 40-95

• Study partner who has some weekly contact with patient. Some of the neuropsychological assessment require collateral from close contacts to assess cognition and functioning. Since neurodegenerative diseases can be associated with reduced cognition, including reduced awareness of one's own impairments, participants will be assessed for their capacity to consent at all study visits.

• Must, in the opinion of the site investigator, be able to complete most study procedures.

Locations
Other Locations
Canada
Baycrest
NOT_YET_RECRUITING
North York
Centre for Addiction and Mental Health
NOT_YET_RECRUITING
Toronto
Sunnybrook Health Sciences Centre
NOT_YET_RECRUITING
Toronto
Toronto Western Hospital, University Health Network
RECRUITING
Toronto
Contact Information
Primary
Claudia Clementi, HBSc
claudia.clementi@uhn.ca
416-603-5914
Time Frame
Start Date: 2023-11-11
Estimated Completion Date: 2027-11
Participants
Target number of participants: 500
Sponsors
Collaborators: Toronto Dementia Research Alliance (TDRA), Baycrest, Centre for Addiction and Mental Health, University of Toronto, Sunnybrook Health Sciences Centre
Leads: University Health Network, Toronto

This content was sourced from clinicaltrials.gov