Entred 2007-2010 - National Representative Sample of people with diabetes 2007-2010 ARCHIVE

Head :
Fosse-Edorh Sandrine

Last update : 07/01/2019 | Version : 1 | ID : 7786

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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 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
Email 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.

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