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

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients aged 18 years and older, undergoing a medical visit in a memory center or neuro-cognition service

• Patients living at home or in housing

• Patients with memory impairment, at all stage of the disease

Locations
Other Locations
France
Hôpital Dugoujon
RECRUITING
Caluire-et-cuire
Centre Hospitalier Lyon Sud
RECRUITING
Lyon
Service de neuro-cognition et neuro-ophtalmologie du Groupement Hospitalier Est
RECRUITING
Lyon
CHU Saint-Etienne
RECRUITING
Saint-etienne
Centre Mémoire de Ressources et de Recherche de Lyon
RECRUITING
Villeurbanne
Contact Information
Primary
Pierre Krolak-Salmon, PhD
pierre.krolak-salmon@chu-lyon.fr
04 72 43 20 50
Time Frame
Start Date: 2020-09-09
Estimated Completion Date: 2032-03-01
Participants
Target number of participants: 5400
Treatments
Experimental: Patients with subjective cognitive complaint or neurocognitive
: Real-life cohort patients with subjective cognitive complaint or neurocognitive disorders undergoing medical examination in memory centers, and for whom extensive evaluations will be performed for the study
Sponsors
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov