Actively Recruiting
Predictive Factors of Autonomy Loss in Real-life Cohort
Led by Hospices Civils de Lyon · Updated on 2022-05-02
5400
Participants Needed
5
Research Sites
598 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Predictive Factors of Autonomy Loss in Real-life Cohort
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- Patients in institution
- Patients under legal protection
- Patients with a hearing or visual impairment, which prevents carrying out examinations
AI-Screening
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Trial Site Locations
Total: 5 locations
1
Hôpital Dugoujon
Caluire-et-Cuire, France, 69300
Actively Recruiting
2
Centre Hospitalier Lyon Sud
Lyon, France, 69310
Actively Recruiting
3
Service de neuro-cognition et neuro-ophtalmologie du Groupement Hospitalier Est
Lyon, France
Actively Recruiting
4
CHU Saint-Etienne
Saint-Etienne, France, 42055
Actively Recruiting
5
Centre Mémoire de Ressources et de Recherche de Lyon
Villeurbanne, France, 69100
Actively Recruiting
Research Team
P
Pierre Krolak-Salmon, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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