France Cancer Barometer - Cross-Sectional Study on Patients Treated in French Healthcare Institutions

Head :
Bonnelye Geneviève
Chabernaud Hélène

Last update : 07/15/2015 | Version : 1 | ID : 8876

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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 Cross-Sectional Study on Patients Treated in French Healthcare Institutions
Sign or acronym France Cancer Barometer
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation 1493177
General Aspects
Medical area Cancer research
Hematology
Pathology (details) By body: epidemiology, current treatments, stage at diagnosis, current stage, patient characteristics (age, sex, ECOG), clinical profile of disease (histology, changes, metastases, etc.)
Health determinants Iatrogenic
Medicine
Keywords clinical profile, agents (chemotherapy/targeted therapy), haematology, oncology, therapeutic strategies
Scientific investigator(s) (Contact)
Name of the director Bonnelye
Surname Geneviève
Address 138 avenue Marx Dormoy - 92120 Montrouge
Phone + 33 (0)1 40 92 47 58
Email genevieve.bonnelye@kantarhealth.com
Organization Kantar Health
Name of the director Chabernaud
Surname Hélène
Address 138 avenue Marx Dormoy - 92120 Montrouge
Phone + 33 (0)1 40 92 24 33
Email Helene.Chabernaud@Kantarhealth.com
Organization Kantar Health
Collaborations
Funding
Funding status Private
Details Kantar Health
Governance of the database
Sponsor(s) or organisation(s) responsible Kantar Health France
Organisation status Private
Additional contact
Main features
Type of database
Type of database Study databases
Study databases (details) Repeated cross-sectional studies (except case control studies)
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. quotas
Database objective
Main objective To determine the epidemiology, clinical profile and therapeutic strategies across 18 procedures (oncology and haematology).
Inclusion criteria Patients currently treated within the active cancer population.
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) 1993
Date of last collection (YYYY or MM/YYYY) 2013
Size of the database
Size of the database (number of individuals) [1000-10 000[ individuals
Details of the number of individuals 4,430
Data
Database activity Data collection completed
Type of data collected Clinical data
Declarative data
Biological data
Clinical data (detail) Direct physical measures
Details of collected clinical data metastases, stage, treatment
Declarative data (detail) Paper self-questionnaire
Face to face interview
Biological data (detail) changes, histology
Presence of a biobank No
Health parameters studied Health event/morbidity
Quality of life/health perception
Others
Quality of life/perceived health (detail) administration criteria, support treatment, healthcare locations, associated anti-tumour treatment, clinical profile (histology, changes, metastases, procedures, stage at diagnosis and current stage).)
Other (detail) administration criteria, support treatment, healthcare locations, associated anti-tumour treatment, clinical profile (histology, changes, metastases, procedures, stage at diagnosis and current stage).
Procedures
Data collection method Face-to-face/self-administered questionnaire/registry/patient data sheets Data collected every 2 years
Quality procedure(s) used ISO 20-232
Participant monitoring No
Links to administrative sources Yes
Linked administrative sources (detail) DREES
Promotion and access
Promotion
Access
Terms of data access (charter for data provision, format of data, availability delay) Contact the scientist in charge at Kantar Health France.
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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