SDSProspective Neuroimaging, Cognition and Behavioural Study of Alzheimer's, Vascular, Parkinson's, Frontotemporal and Mixed Dementias
Data Collection
Collected from today forward - ProspectiveMental Disorders+3
+ Brain Diseases
+ Central Nervous System Diseases
Ecologic or Community
Assessing exposures and health outcomes at the community level in order to identify population-wide health trends.Summary
Study start date: September 1, 1995
Actual date on which the first participant was enrolled.The prospect of disease-modifying therapies in the pipeline for Alzheimer's Disease (AD) has intensified efforts to use brain imaging more effectively for diagnosis and monitoring of dementing illnesses. There is also emerging awareness of the destructive interplay between AD and Cerebrovascular Disease (CVD) in our aging population; both disorders share common vascular risk factors and may respond to similar prevention treatments. Brain mapping techniques capitalize on the fact that different neurodegenerative diseases target particular brain areas. Brain shrinkage and stroke disease can be quantified on Magnetic Resonance Imaging (MRI) using computerized analysis. This ongoing study applies advanced MR imaging analysis, genetic testing and standardized cognitive and functional assessments done at yearly intervals to measure and monitor longitudinal change in patients with AD, vascular and other neurodegenerative diseases and potentially to measure modifying effects of emerging therapies. Nearly 1800 patients (Mild Cognitive Impairment or dementia from AD, Vascular, Frontotemporal or Lewy Body Disease) and over 140 normal elderly have already been enrolled, with 180 autopsies. This study utilizes specialized imaging analysis software packages to reliably quantify brain tissue volumes and small vessel disease, the most common type of CVD. The SDS also investigates other potential biomarkers of dementia such as eye-tracking, optical coherence tomography, gait and balance, and the gut microbiome to explore their clinical utility. Results from this study will help to improve diagnosis, to customize treatment, and to better monitor disease-modifying therapies currently under investigation should they become applicable to everyday practice.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.1800 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Ecologic or Community
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 40 to 90 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Patient Inclusion Criteria (General): Age between 40 and 90 (inclusive) Fluent in English Completed 8 years of education or higher Visual and auditory acuity adequate for neuropsychological testing Mini-Mental State Exam (MMSE) score ≥ 16 Patient Exclusion Criteria (General): Possible secondary causes of dementia, concomitant or history of neurological or psychiatric illness (other than stroke or Parkinsonism) History of alcohol or substance abuse or dependence within the past 2 years Normal Control Inclusion Criteria: Age between 40-90 Fluent in English Completed 8 years of education or higher No significant memory complaints Normal Control Exclusion Criteria: Being treated or history of being treated for psychiatric or neurological illness History of alcohol or substance abuse or dependence within the past 2 years Current use of psychoactive medications (e.g. antidepressant, neuroleptics, chronic anxiolytics or sedative hypnotics, etc.) Medical contraindications to MRI
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.8 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Sunnybrook Health Sciences Centre
Toronto, CanadaOpen Sunnybrook Health Sciences Centre in Google Maps