Entred 2007-2010 - National Representative Sample of people with diabetes 2007-2010 
Head :
Fosse-Edorh Sandrine
Last update : 07/01/2019 | Version : 1 | ID : 7786
| General | |
| Identification | |
| Detailed name | National Representative Sample of people with diabetes 2007-2010 |
| Sign or acronym | Entred 2007-2010 |
| CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation | 907172 |
| General Aspects | |
| Medical area |
Endocrinology and metabolism |
| Health determinants |
Lifestyle and behavior |
| Keywords | type 1 diabetes, vascular risk, socioeconomic level, socioeconomic status, educational measures, quality of care, cost, type 2 diabetes, characteristics, complication, hospitalisation, mortality |
| Scientific investigator(s) (Contact) | |
| Name of the director | Fosse-Edorh |
| Surname | Sandrine |
| Address | 12 rue du Val d’Osne 94415 Saint Maurice Cedex |
| Phone | + 33 (0)1 55 12 53 14 |
| s.fosse@invs.sante.fr | |
| Organization | INVS - Institut de Veille |
| Collaborations | |
| Funding | |
| Funding status |
Public |
| Details | InVS, CnamTS, RSI, HAS, INPES. |
| Governance of the database | |
| Sponsor(s) or organisation(s) responsible | INVS - Institut de Veille Sanitaire |
| Organisation status |
Public |
| Additional contact | |
| Main features | |
| Type of database | |
| Type of database |
Study databases |
| Study databases (details) |
Not-repeated cross-sectional studies (except case control studies) |
| Database recruitment is carried out by an intermediary |
An administrative base or a register |
| Database recruitment is carried out as part of an interventional study |
No |
| Additional information regarding sample selection. | Sample is based on a random selection of personal keys in the Local Health Insurance databases. The sample consists of individuals with these keys who have received at least three reimbursements for oral antidiabetic medications and/or insulin over the last twelve months. |
| Database objective | |
| Main objective | To describe the characteristics of people pharmacologically treated for diabetes, their health with regards to diabetes, the quality of care received, treatment plan and self-management education; their quality of life, experiences and requirements in terms of education and information, as well as the cost of diabetes. |
| Inclusion criteria | Beneficiaries of the French general scheme of health insurance (CNAMTS) (excluding local mutualist sections) and the Independent Scheme for employees (RSI); residing in mainland France or overseas départements (DOM); and who have received at least three reimbursements for oral antidiabetic medications and/or insulin over the last twelve months. |
| Population type | |
| Age |
Newborns (birth to 28 days) Infant (28 days to 2 years) Early childhood (2 to 5 years) Childhood (6 to 13 years) Adolescence (13 to 18 years) Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) 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 | France |
| Data collection | |
| Dates | |
| Date of first collection (YYYY or MM/YYYY) | 08/2006 |
| Date of last collection (YYYY or MM/YYYY) | 07/2009 |
| Size of the database | |
| Size of the database (number of individuals) |
[10 000-20 000[ individuals |
| Details of the number of individuals | 8,000 people in metropolitan France, 800 people from overseas départements and 850 children. |
| Data | |
| Database activity |
Data collection completed |
| Type of data collected |
Clinical data Declarative data Biological data Administrative data |
| Clinical data (detail) |
Direct physical measures |
| Details of collected clinical data | Medical questionnaire sent to attending physicians. |
| Declarative data (detail) |
Paper self-questionnaire Phone interview |
| Details of collected declarative data | Self-administered patient questionnaire and phone questionnaire administered by National Health Insurance medical officers. |
| Biological data (detail) | Medical questionnaire sent to physicians. |
| Administrative data (detail) | Medical consumption, hospitalisation data and mortality data. |
| Presence of a biobank |
No |
| Health parameters studied |
Health event/morbidity Health event/mortality Health care consumption and services Quality of life/health perception |
| Care consumption (detail) |
Hospitalization Medical/paramedical consultation Medicines consumption |
| Procedures | |
| Data collection method | Data collected by self-administered questionnaire, phone questionnaire and physician questionnaire, combined with passive medical and administrative data collection (medical consumption and hospitalisation) and mortality data (vital status and cause of death). |
| Classifications used | CIM 10. |
| Participant monitoring |
Yes |
| Details on monitoring of participants | Passive medical and administrative data collection (medical consumption and hospitalisation) for two years and mortality data (vital status and cause of death). |
| Links to administrative sources |
Yes |
| Linked administrative sources (detail) | Local medical consumption data, PMSI, RNIPP and CépiDC. |
| Promotion and access | |
| Promotion | |
| Link to the document | principales publications.docx |
| Access | |
| Terms of data access (charter for data provision, format of data, availability delay) |
The results are published as reports, summaries and articles. Complete bibliography on the ENTRED website..
Data are available to external teams after project is submitted to an assessment committee. |
