SOHO-France - Cohort of Schizophrenic Patients Receiving Antipsychotic Drugs ARCHIVE

Head :
Gasquet Isabelle

Last update : 09/05/2017 | Version : 1 | ID : 73154

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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 Cohort of Schizophrenic Patients Receiving Antipsychotic Drugs
Sign or acronym SOHO-France
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation CNIL
General Aspects
Medical area Disability/handicap
Psychology and psychiatry
Pathology (details) Schizophrenia
Health determinants Genetic
Iatrogenic
Lifestyle and behavior
Medicine
Keywords antipsychotic, remission, schizophrenia, relapse, treatment
Scientific investigator(s) (Contact)
Name of the director Gasquet
Surname Isabelle
Phone +33 (0)1 40 27 31 85
Email isabelle.gasquet@pbr.ap-hop-paris.fr
Organization Paris Public Hospitals
Collaborations
Funding
Funding status Private
Details Lilly France pharmaceutical laboratory
Governance of the database
Sponsor(s) or organisation(s) responsible Assistance publique–hôpitaux de Paris
Organisation status Public
Additional contact
Main features
Type of database
Type of database Study databases
Study databases (details) Cohort study
Database recruitment is carried out by an intermediary A selection of health care professionals
Database recruitment is is made on the basis of: Medication(s) taken
Database recruitment is carried out as part of an interventional study No
Additional information regarding sample selection. Patients were recruited by psychiatrists drawn from the LOGIMED (IMS Health) and TVF (CEGEDIM) sampling frame with layering according to activity type (private versus hospital practice or mixed) and area of practice. Each psychiatrist must recruit four patients consecutively: two patients receiving olanzapine and two patients receiving an anti-psychotic prescribed at the discretion of the treating psychiatrist from available treatment (risperidone, amisulpride, clozapine, typical oral antipsychotics and intramuscular, long-acting medication).
Database objective
Main objective To provide information on patients monitored as outpatients, regardless of antipsychotic treatment received and to provide answers, especially regarding treatment adherence and remission rates, as well as relapse rates over a three-year monitoring period.
Inclusion criteria Schizophrenic adult patients monitored as outpatients and randomly recruited by psychiatrists.
Population type
Age 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) 2001
Date of last collection (YYYY or MM/YYYY) 2005
Size of the database
Size of the database (number of individuals) [500-1000[ individuals
Details of the number of individuals 964
Data
Database activity Data collection completed
Type of data collected Clinical data
Declarative data
Clinical data (detail) Direct physical measures
Details of collected clinical data History of illness, previous and ongoing treatments, symptomatology (Clinical Global Impression – Schizophrenia [CGI-SCH] scale) and a Visual Analogue Scale [VAS]). Clinical severity was measured by the CGI-SCH scale.
Declarative data (detail) Face to face interview
Details of collected declarative data Demographic data, quality of life (EuroQol scale of five items [EQ-5D]; addictive comorbidities in the form of simple questions on past and current use of illicit substances and alcohol; social status (accommodation type, type of work activity, number of social activities, etc.)
Presence of a biobank No
Health parameters studied Health care consumption and services
Care consumption (detail) Medicines consumption
Procedures
Participant monitoring Yes
Details on monitoring of participants Follow-up at three and six months then every six months for three years.
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://www.ncbi.nlm.nih.gov/pubmed/19162420
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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