REAL.FR - Longitudinal Study on Patients in Alzheimer's Disease Network ARCHIVE

Head :
Vellas Bruno, Inserm U 1027

Last update : 09/05/2017 | Version : 2 | ID : 8787

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Métadonnées
Identification
General Aspects
Scientific investigator(s) (Contact)
Collaborations
Funding
Governance of the database
Additional contact
Type of database
Database objective
Population type
Dates
Size of the database
Data
Procedures
Promotion
Access
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General
Identification
Detailed name Longitudinal Study on Patients in Alzheimer's Disease Network
Sign or acronym REAL.FR
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation CNIL approval.
General Aspects
Medical area Geriatrics
Neurology
Health determinants Genetic
Keywords healthcare sector, institutionalisation, network
Scientific investigator(s) (Contact)
Name of the director Vellas
Surname Bruno
Address CHU de Toulouse GERONTOPOLE 170, Avenue de Caselardit TSA 40031 31059 Toulouse Cédex 09
Phone +33 (0)5 61 77 64 25
Email vellas.b@chu-toulouse.fr
Unit Inserm U 1027
Organization CHU de
Collaborations
Funding
Funding status Public
Details Ministry of Health.
Governance of the database
Sponsor(s) or organisation(s) responsible CHU de Toulouse
Organisation status Public
Additional contact
Main features
Type of database
Type of database Study databases
Study databases (details) Longitudinal study (except cohorts)
Database recruitment is carried out by an intermediary A selection of health institutions and services
Database recruitment is carried out as part of an interventional study No
Additional information regarding sample selection. The study population consists of patients with Alzheimer's-type dementia.
Database objective
Main objective To ensure regular monitoring of the patient and those close to them in order to assess the cognitive and non-cognitive aspects of the disease.
To analyse treatment methods, as well as drug- and non-drug-related therapy for elderly people with AD across a national sample with diverse socio-cultural contexts. To identify potential treatment issues, such as repeated hospitalisation or emergency institutionalisation.
Inclusion criteria - Male and female;
- Patient with Alzheimer's-type dementia.
Population type
Age Elderly (65 to 79 years)
Great age (80 years and more)
Population covered Sick population
Gender Male
Woman
Geography area National
Detail of the geography area 16 university hospital centres for geriatrics, neurology and psychiatry.
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 2000
Date of last collection (YYYY or MM/YYYY) 2002
Size of the database
Size of the database (number of individuals) [500-1000[ individuals
Details of the number of individuals 700
Data
Database activity Data collection completed
Type of data collected Declarative data
Paraclinical data
Declarative data (detail) Face to face interview
Details of collected declarative data Case report form: sociodemographic data, medical and surgical history, date of initial symptoms and disease diagnosis age, current list of medication taken, list of different psychotropic or specific disease treatments, ADL and IADL autonomy assessment, overall assessment of cognitive function by MMS and ADAS-Cog, assessment of dementia stage by Reisberg GDS and CDR, assessment of patient's behavioural problems by NPI, nutritional status assessment using MNA, balance disorder assessment (one-leg balance, living arrangement, use of home care service, such housekeeping, home nursing care, private nurse, use of private paid help such a domestic worker, overnight care, cleaning lady, home meal deliveries, allowances received for dependent elderly people (Prestation Spécifique Dépendance [Specific Dependency Benefit], Allocation Personnalisée d'Autonomie [Personal Autonomy Allowance]), sources of income (retirement, family or caregiver support, various allowances, pensions), level of education (level of education, the highest qualification obtained), former occupation(s).
Paraclinical data (detail) - Brain scan - thyroid assessment.
Presence of a biobank No
Health parameters studied Health event/morbidity
Quality of life/health perception
Procedures
Data collection method Data is collected during visits carried out over 6 months in university hospital centres participating in the study. Data are gathered through a case report form by a medical team trained to administer different tests.
Participant monitoring Yes
Details on monitoring of participants Follow-up over 4 years.
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://tinyurl.com/Hal-REAL-FR
Description List of publications in HAL
Link to the document http://www.ncbi.nlm.nih.gov/pubmed/?term=Vellas+B[author]+AND+%28REAL.FR+OR+REAL-FR%29
Description List of publications in Pubmed
Access
Terms of data access (charter for data provision, format of data, availability delay) Contact the scientist in charge.
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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