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Predictive Factors of Autonomy Loss in Real-life Cohort — MEM-AURA  

Memory Disorders Clinical Trial

Official title:
Predictive Factors Associated With Impairment in Functional Autonomy in a Regional Real-life Cohort of Patients With Alzheimer's Disease or Related Disorders (ADRD)

Clinical Trial Summary

The Alzheimer's disease or related disorders (ADRD) are among the most disabling diseases because of their main features such as cognitive impairment, loss of functional autonomy and behavioural disorders. In absence of current curative treatment, the identification of the predictive risk factors of progression of the disease, evaluated through its main symptoms, represents a major stake of public health. The Investigators aim at developing a regional database, which includes the patient medical records on a prospective basis, in collaboration with the medical and administrative staff and with the University hospital computer science departments. The main objective is to study the predictive factors associated with change in functional autonomy level, measured every 6 to 12 months in centres across Region Auvergne Rhone-Alpes in France. The real-life study population will consist in about 5400 patients with ADRD. The inclusion period will be of 3 years, the length of follow-up of each patient will be of 10 years max for a total study length of 13 years.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03894254
Study type Interventional
Source Hospices Civils de Lyon
Contact Pierre Krolak-Salmon, PhD
Phone 04 72 43 20 50
Email pierre.krolak-salmon@chu-lyon.fr
Status Recruiting
Phase N/A
Start date September 9, 2020
Completion date March 1, 2032
View Details
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