EVALHOSPITAM OR EVHAN - Evaluation of hospitalisation for patients with anorexia nervosa: Efficacy of treatment and research predictive outcome factors ARCHIVE

Head :
Godart Nathalie, U669 INSERM TROUBLES DES CONDUITES DE L'ADOLESCENT

Last update : 03/01/2020 | Version : 2 | ID : 60159

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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 Evaluation of hospitalisation for patients with anorexia nervosa: Efficacy of treatment and research predictive outcome factors
Sign or acronym EVALHOSPITAM OR EVHAN
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation CNIL : 25/09/2009
General Aspects
Medical area Psychology and psychiatry
Health determinants Addictions
Nutrition
Social and psychosocial factors
Keywords clinical outcome, Morgan and Russell scale, body mass index, menstruation, somatic complications, psychiatric complications, social adjustment, treatment received, Health episodes, mortality
Scientific investigator(s) (Contact)
Name of the director Godart
Surname Nathalie
Address 75014 PARIS
Phone + 33 (0)1 56 61 69 35
Email nathalie.godart@imm.fr
Unit U669 INSERM TROUBLES DES CONDUITES DE L'ADOLESCENT
Organization INSERM - Institut National de Santé et Recherche
Collaborations
Funding
Funding status Mixed
Details Contrat d'interface INSERM, PHRC 2006, ANR JEUNE CHERCHEUR 2007, CNAM, contrat CIFRE, bourse EIFFEL, fondation de France
Governance of the database
Sponsor(s) or organisation(s) responsible INSTITUT MUTUALISTE MONSOURIS
Organisation status Public
Additional contact
Main features
Type of database
Type of database Study databases
Study databases (details) Longitudinal study (except cohorts)
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. Prospective Other bodies active in creating this cohort: CHU AND CHG and research laboratory. Closing date for inclusion: 01/03/2010
Database objective
Main objective General objective: to evaluate the impact (efficacy) of five different inpatient treatment modalities for anorexia nervosa. Individual global health outcome (physical, psychiatric, nutritional and social) will be measured on a short-term basis (on discharge), as well as hospital treatment meeting or exceeding statutory charges on a medium term basis (12 months), taking into account confounding factors and recognised prognostic factors. Global health is evaluated using the Morgan and Russell scale as well as secondary criteria for deteriorating health (see evaluation criteria methodology). Secondary objectives: - to determine predictive factors for failures in inpatient treatment, duration of hospitalisation, and treatment costs using clinical epidemiology methodology. - to begin a long-term prospective study to evaluate the psychological, physical, nutritional and social outcome of a homogeneous cohort of subjects suffering from severe anorexia nervosa. - two "ancillary" biological sub-projects: - to evaluate the development of depressive and anxiety symptoms in relation to changes in clinical nutritional status and serotonin markers - to evaluate cellular immunity development in relation to changes in clinical nutrition.
Inclusion criteria - Patients between 8 and 65 years old; - patients hospitalised for anorexia nervosa (who only receive treatment by necessity of somatic condition: rapid weight loss, or significantly underweight with a BMI of less than 15, or their psychological condition), as well as parents of minor and adult patients still living at home; - obtained written consent; - patients not covered by social security health insurance.
Population type
Age 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)
Population covered Sick population
Gender Male
Woman
Geography area National
Detail of the geography area Multicentric cohort throughout France (11 centres): Île-de-France: 6 centres, Bordeaux: 2 centres, Nantes: 1 centre, Rouen: 1 centre, Saint-Étienne: 1 centre.
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 03/2009
Date of last collection (YYYY or MM/YYYY) 03/2010
Size of the database
Size of the database (number of individuals) < 500 individuals
Details of the number of individuals 180
Data
Database activity Data collection completed
Type of data collected Declarative data
Biological data
Declarative data (detail) Face to face interview
Biological data (detail) Type of samples collected: all analysis during hospitalisation (standard protocol), serotonin, tryptophan, CD4/CD8.
Presence of a biobank No
Health parameters studied Health event/morbidity
Health event/mortality
Procedures
Data collection method Self-administered questionnaire: direct input Interview: direct input Clinical examinations: direct input Biological analysis: direct input
Participant monitoring Yes
Details on monitoring of participants (Indefinite duration)
Links to administrative sources Yes
Linked administrative sources (detail) CépiDc
Promotion and access
Promotion
Link to the document http://tinyurl.com/Hal-EVALHOSPITAM-EVHAN
Description Liste des publications dans HAL
Link to the document http://www.ncbi.nlm.nih.gov/pubmed/?term=EVALHOSPITAM+OR+EVHAN+OR+22378228[uid]
Description Liste des publications dans Pubmed
Access
Terms of data access (charter for data provision, format of data, availability delay) To be decided if data may be used by academic teams. Data may not be used by industrial teams.
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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