Last update : 06/10/2015 | Version : 1 | ID : 22114
General | |
Identification | |
Detailed name | Case-control study of patients attending a dermatologist: risk factors for seborrheic dermatitis |
Sign or acronym | EPIDERMAS: epidemiological survey on seborrheic dermatitis risk factors |
General Aspects | |
Medical area |
Dermatology, venereology |
Health determinants |
Genetic Lifestyle and behavior |
Keywords | Risk factors, impact, stress, alcohol, tobacco |
Scientific investigator(s) (Contact) | |
Name of the director | Chosidow |
Surname | Olivier |
Address | 51 Avenue du Maréchal de Lattre de Tassigny 94010 Créteil |
Phone | +33 (0)1 49 81 25 01 |
olivier.chosidow@hmn.aphp.fr | |
Unit | CIC1430 CIC HENRI MONDORÉquipe/activité : Module plurithématique |
Organization | AP-HP |
Collaborations | |
Funding | |
Funding status |
Public |
Details | APHP |
Governance of the database | |
Sponsor(s) or organisation(s) responsible | AP-HP |
Organisation status |
Public |
Additional contact | |
Main features | |
Type of database | |
Type of database |
Study databases |
Study databases (details) |
Case control study |
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. | Cases with sporadic or non-sporadic seborrheic dermatitis are selected and controls are matched according to age (+/- 5 years) and gender that are attending consultation for another reason (except psoriasis and eczema). |
Database objective | |
Main objective | To analyse risk factors for seborrheic dermatitis and risk factors for a flare-ups. To assess the impact of seborrheic dermatitis on quality of life. |
Inclusion criteria |
- male and female
- adult - patient attending a dermatologist |
Population type | |
Age |
Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) |
Population covered |
General population |
Gender |
Male Woman |
Geography area |
National |
Detail of the geography area | France |
Data collection | |
Dates | |
Date of first collection (YYYY or MM/YYYY) | 10/2005 |
Date of last collection (YYYY or MM/YYYY) | 12/2011 |
Size of the database | |
Size of the database (number of individuals) |
< 500 individuals |
Details of the number of individuals | 380: - 190 cas/cases - 190 témoins/controls |
Data | |
Database activity |
Data collection completed |
Type of data collected |
Clinical data Declarative data |
Clinical data (detail) |
Medical registration |
Details of collected clinical data | Consultation with dermatologist. |
Declarative data (detail) |
Paper self-questionnaire |
Details of collected declarative data | Sociodemographic characteristics, disease parameters and exposure to risk factors in the months preceding consultation with dermatologist. |
Presence of a biobank |
No |
Health parameters studied |
Health event/morbidity Quality of life/health perception |
Procedures | |
Data collection method | Data are collected with questionnaires: the questionnaire is completed by the physician and the self-administered questionnaire is completed by the patient. |
Participant monitoring |
No |
Links to administrative sources |
No |
Promotion and access | |
Promotion | |
Link to the document | http://www.sciencedirect.com/science/article/pii/S0151963814008746 |
Link to the document | http://www.sciencedirect.com/science/article/pii/S0151963814008746 |
Link to the document | http://www.sciencedirect.com/science/article/pii/S0151963814008746 |
Link to the document | http://www.sciencedirect.com/science/article/pii/S0151963814008746 |
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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