PHOENIX - Cohort on the scalable process of post traumatic stress disorders : The involvement of stress regulation systems and the role of allostatic load ARCHIVE

Head :
Chaudieu Isabelle, Inserm U1061

Last update : 06/01/2020 | Version : 1 | ID : 8566

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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 on the scalable process of post traumatic stress disorders : The involvement of stress regulation systems and the role of allostatic load
Sign or acronym PHOENIX
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation CNIL n°1095744 (30/08/2005). CPP : PROM 7806-n°05 01 02 (01/02/2005)
General Aspects
Medical area Endocrinology and metabolism
Psychology and psychiatry
Pathology (details) Affective disorder : post traumatic stress disorder Predictive value of biological and clinical stress markers in the development of PTSD
Keywords Post traumatic stress disorder, psychiatric co-morbidities, allostatic load, biologic markers, stress regulation systems, clinical research, epidemiological and prospective research, resilience, PTSD, cortisol, cohort
Scientific investigator(s) (Contact)
Name of the director Chaudieu
Surname Isabelle
Address Hôpital la Colombière, 39 avenue Charles Flahault, Pavillon 42. 34093 MONTPELLIER cedex 5
Phone + 33 (0)4 99 61 45 78
Email isabelle.chaudieu@inserm.fr
Unit Inserm U1061
Organization INSERM
Collaborations
Participation in projects, networks and consortia Yes
Details ABC of psychotraumas, Biological & clinic approches
Funding
Funding status Public
Details PHRC régional 2004
Governance of the database
Sponsor(s) or organisation(s) responsible Promoteur/financeur : PHRC régional CHU de Montpellier
Organisation status Public
Sponsor(s) or organisation(s) responsible Coordinateur scientifique : Inserm U1061
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 institutions and services
Database recruitment is carried out as part of an interventional study No
Additional information regarding sample selection. - Medical and paramedical examinations
- Medicines
Database objective
Main objective The main goal of the project is to study the psychological consequences of violent trauma and the predictive value of biological and clinical stress markers in the development of PTSD
The specific objectives are :
1) To evaluate the allostatic load level and its development over time
2) To evaluate the prevalence of PTSD and other psychiatric co-morbidities (as depression) on subjects who did endure severe events
3) To determine if the allostatic load level is in link with a chronical development of a post traumatic stress disorder
Inclusion criteria -women and men aged 18 to 75 years
-person who have experienced a traumatic event during the previous week (0 to 7 days before)
-type of events : physical assault, sexual assault, work accident, road accident, natural disaster.
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
Gender Male
Woman
Geography area Local
French regions covered by the database Languedoc-Roussillon Midi-Pyrénées
Detail of the geography area Montpellier and its surroundings
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 05/2005
Date of last collection (YYYY or MM/YYYY) 06/2010
Size of the database
Size of the database (number of individuals) < 500 individuals
Details of the number of individuals 124
Data
Database activity Data collection completed
Type of data collected Clinical data
Declarative data
Biological data
Clinical data (detail) Medical registration
Declarative data (detail) Paper self-questionnaire
Face to face interview
Phone interview
Biological data (detail) Biological data at visit 1, 3 and 4 : - Blood samples : cholesterol, HbA1c, albumin, CRP, orosomucoid - Urine samples : cortisol, adrenaline, norepinephrine
Presence of a biobank Yes
Contents of biobank Serum
Details of biobank content 1 ml of serum by subject
Health parameters studied Health event/morbidity
Health care consumption and services
Others
Care consumption (detail) Medical/paramedical consultation
Medicines consumption
Other (detail) Resilience Predictive biological markers
Procedures
Data collection method - Resilience - Predictive biological markers
Classifications used DSM IV
Participant monitoring Yes
Details on monitoring of participants - Visit 1 (day 1) : clinical psychiatric examination, blood and urine samples, psychometric measures , self and administrated-reported scales - Visit 2 (1 month) : self and administrated-reported scales - Visit 3 (4 month) : clinical psychiatric examination, blood and urine samples, psychometric measures, self and administrated-reported scales - Visit 4 (1 year) : clinical psychiatric examination, blood and urine samples, psychometric measures, self and administrated-reported scales
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://www.ncbi.nlm.nih.gov/pubmed/22768152
Link to the document http://www.ncbi.nlm.nih.gov/pubmed/22768152
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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