SDSProspective Neuroimaging, Cognition and Behavioural Study of Alzheimer's, Vascular, Parkinson's, Frontotemporal and Mixed Dementias
Colección de datos
Recopilados desde hoy en adelante - ProspectivoTrastornos Mentales+2
+ Enfermedades del Cerebro
+ Enfermedades del Sistema Nervioso Central
Ecológico o Comunitario
Evaluación de exposiciones y resultados de salud a nivel comunitario para identificar tendencias de salud en la población.Resumen
Fecha de inicio: 1 de septiembre de 1995
Fecha en la que se inscribió al primer participante.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.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 1800 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Ecológico o Comunitario
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.De 40 a 90 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
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
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.8 grupos de intervención están designados en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Objetivos del Estudio
Objetivos Primarios
Objetivos Secundarios
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene una ubicación
Sunnybrook Health Sciences Centre
Toronto, CanadaAbrir Sunnybrook Health Sciences Centre en Google Maps