NHWS - National Health and Wellness Survey in France

Head :
Bonnelye Geneviève

Last update : 01/04/2021 | Version : 2 | ID : 8472

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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 Health and Wellness Survey in France
Sign or acronym NHWS
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation International database submitted to IRB in the USA
General Aspects
Medical area Cancer research
Cardiology
Dermatology, venereology
Disability/handicap
Endocrinology and metabolism
Gastroenterology et hepatology
General practice
Gynecology/ obstetrics
Infectious diseases
Internal medicine
Neurology
Ophthalmology
Otolaryngology or ENT
Physical medicine and rehabilitation
Pneumology
Psychology and psychiatry
Rheumatology
Study of allergies
Urology, andrology and nephrology
Study in connection with Covid-19 No
Health determinants Geography
Iatrogenic
Lifestyle and behavior
Medicine
Occupation
Keywords impact of illness on work, choice of treatment, undiagnosed sufferers, treatment adherence, resources, healthcare approach, quality of life. satisfaction, Condition, diagnosis, symptoms, attitudes
Scientific investigator(s) (Contact)
Name of the director Bonnelye
Surname Geneviève
Address 3 avenue Pierre Masse 75014 Paris
Phone +33 (0)1 40 92 66 66
Email genevieve.bonnelye@kantar.com
Organization Kantar Health
Collaborations
Funding
Funding status Private
Details Kantar Health
Governance of the database
Sponsor(s) or organisation(s) responsible Kantar Health
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 population file
Database recruitment is carried out as part of an interventional study No
Additional information regarding sample selection. quotas
Database objective
Main objective Health and impact from a humanistic and economic standpoint (primary data/200 identified pathologies)
Objectives: scientific publications and provision of economic models
Inclusion criteria France: national sample of 15,000 French individuals aged 18 and over and representative in terms of gender, age, region, metropolitan area and socio-professional category.
Population type
Age Adulthood (19 to 24 years)
Adulthood (25 to 44 years)
Adulthood (45 to 64 years)
Elderly (65 to 79 years)
Population covered General population
Pathology
Gender Male
Woman
Geography area International
Detail of the geography area Brazil, China, Germany, Italy, France, Japan, Russia, Spain, South Korea, Taiwan, United Kingdom and United States
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 2000
Date of last collection (YYYY or MM/YYYY) 2020
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals 15,000 individuals in France, 250,000 individuals across all countries
Data
Database activity Current data collection
Type of data collected Declarative data
Utility / preference data
Declarative data (detail) Internet self-questionnaire
Utility / preference data (detail) EQ-5D
Presence of a biobank No
Health parameters studied Health event/morbidity
Health care consumption and services
Quality of life/health perception
Others
Care consumption (detail) Hospitalization
Medical/paramedical consultation
Medicines consumption
Other (detail) Validates scales : EQ-5D, SF36/SF12, WPAI and 30+ Disease-Specific PROs
Procedures
Data collection method online/recruitment by telephone for populations aged 65 and over
Quality procedure(s) used ISO 20252
Participant monitoring No
Followed pathology
Links to administrative sources No
Promotion and access
Promotion
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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