Last update : 06/28/2014 | Version : 1 | ID : 60164
| General | |
| Identification | |
| Detailed name | Ageing and Independent Living |
| Sign or acronym | VIVA |
| CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation | Accord CNIL |
| General Aspects | |
| Medical area |
Geriatrics |
| Health determinants |
Social and psychosocial factors |
| Others (details) | Ageing |
| Keywords | life expectancy, incapacity, physical independence, cognitive disease, Health episodes, psychological, prevention |
| Scientific investigator(s) (Contact) | |
| Name of the director | Jeandel |
| Surname | Claude |
| Address | 34295 MONTPELLIER |
| Phone | + 33 (0)4 67 33 67 78 |
| claudejeandel@yahoo.fr | |
| Unit |
Pôle de gérontologie Centre de prévention et de traitement des maladies du vieillissement CHRU Montpellier |
| Organization | CHRU |
| Name of the director | Cassou |
| Surname | Bernard |
| Address | 75016 PARIS |
| Phone | + 33 (0)1 44 96 32 04 |
| bernard.cassou@spr.aphp.fr | |
| Unit |
LABORATOIRE UNIVERSITAIRE SANTÉ-VIEILLISSEMENT EA 2506 UFR PARIS-ILE DE FRANCE- OUEST (UVSQ) |
| Organization | AP - |
| Name of the director | Duchêne |
| Surname | Jacques |
| Address | 10010 TROYES |
| Phone | + 33 (0)3 25 71 76 04 |
| jacques.duchene@utt.fr | |
| Unit | INSTITUT CHARLES DELAUNAY (FRE CNRS 2848) |
| Organization | INSTITUT CHARLES |
| Collaborations | |
| Participation in projects, networks and consortia |
Yes |
| Funding | |
| Funding status |
Private |
| Details | INSTITUTIONS DE RETRAITE COMPLÉMENTAIRE SOUS LA TUTELLE DE L'AGIRC ET DE L'ARRCO |
| Governance of the database | |
| Sponsor(s) or organisation(s) responsible | CHU Montpellier |
| Organisation status |
Public |
| Additional contact | |
| Main features | |
| Type of database | |
| Type of database |
Study databases |
| Study databases (details) |
Cohort study |
| Database recruitment is carried out by an intermediary |
A population file |
| Database recruitment is carried out as part of an interventional study |
Yes |
| Details |
Performed at group level (clusters) |
| Additional information regarding sample selection. | Prospective Other bodies active in creating this cohort: AGIRC-ARROC PREVENTION CENTRES |
| Database objective | |
| Main objective | General objective: to measure the impact of prevention assessments and subsequent recommendations from a medical, psychological, and social perspective on health and quality of life (carried out in AGIRC-ARRCO Prevention Centres). Secondary objectives: Objectives are two-fold: - in-depth study: 1 - to improve the sharing of knowledge between different assessment specialists through computerised questionnaires; 2 - to implement a specific evaluation to identify predictive frailty factors in a sub-group of 75 years and over. - board study 1 - to evaluate participating volunteers' interest and need for new technologies to ensure quality of life at home; 2 - to welcome external research projects from other structures. |
| Inclusion criteria | Following invitation, participation is on a voluntary basis. Mailing is carried out on submission of retirement file by social services from supplementary retirement institutions. |
| Population type | |
| Age |
Elderly (65 to 79 years) Great age (80 years and more) |
| Population covered |
General population |
| Gender |
Male Woman |
| Geography area |
National |
| Detail of the geography area | Multicentric cohort throughout France (10 centres) - Grenoble, Lyon, Marseilles, Paris*2, Rouen, Toulouse, Troyes, Valence and certain centres with local regional offices |
| Data collection | |
| Dates | |
| Date of first collection (YYYY or MM/YYYY) | 01/2010 |
| Size of the database | |
| Size of the database (number of individuals) |
[10 000-20 000[ individuals |
| Details of the number of individuals | 10000 sujets de plus de 55 ans/ more than 55 years (étude modification du comportement et conséquences) ; 1000 sujets de 75 ans / more than 75 years (groupe fragilité) |
| Data | |
| Database activity |
Data collection completed |
| Type of data collected |
Clinical data Declarative data Paraclinical data Biological data |
| Clinical data (detail) |
Direct physical measures Medical registration |
| Declarative data (detail) |
Paper self-questionnaire Face to face interview |
| Paraclinical data (detail) | Weight, height, waist circumference |
| Biological data (detail) | Type of samples taken: biological analysis is carried out in partnership with health insurance health examination centres (CES) |
| Presence of a biobank |
No |
| Health parameters studied |
Health event/morbidity Health event/mortality Quality of life/health perception |
| Procedures | |
| Data collection method | Self-administered questionnaire: Direct input Interview: Direct input Clinical examination: Direct input Biological analysis: Direct input |
| Participant monitoring |
Yes |
| Details on monitoring of participants | (Indefinite duration) |
| Links to administrative sources |
Yes |
| Linked administrative sources (detail) | Database(s) used: Other health insurance databases |
| Promotion and access | |
| Promotion | |
| Access | |
| Terms of data access (charter for data provision, format of data, availability delay) | Data may be used by academic teams: temporary access depending on field Data may be used by industrial teams: contractual access |
| Access to aggregated data |
Access on specific project only |
| Access to individual data |
Access on specific project only |
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