ITMO Santé Publique
ITMO Santé Publique
Date de modification : 01/01/2018 | Version : 1 | ID : 166
| Général | |
| Identification | |
| Nom détaillé | Validation of the ACT questionnaire in general practice |
| Sigle ou acronyme | ATHMOS |
| Numéro d'enregistrement (ID-RCB ou EUDRACT, CNIL, CPP, etc.) | CNIL n°90 60 78 (12/05/2006) |
| Thématiques générales | |
| Domaine médical |
Pneumology |
| Autres, précisions | Asthma |
| Mots-clés | asthma, control, "Asthma Control Test ©" (ACT) |
| Responsable(s) scientifique(s) | |
| Nom du responsable | Pribil |
| Prénom | Céline |
| Téléphone | +33 (0)1 39 17 90 62 |
| celine.c.pribil@gsk.com | |
| Laboratoire | Laboratoire GSK |
| Collaborations | |
| Financements | |
| Financements |
Private |
| Précisions | GSK laboratory |
| Gouvernance de la base de données | |
| Organisation(s) responsable(s) ou promoteur | Laboratoire GSK |
| Statut de l’organisation |
Secteur Privé |
| Contact(s) supplémentaire(s) | |
| Caractéristiques | |
| Type de base de données | |
| Type de base de données |
Study databases |
| Base de données issues d'enquêtes, précisions |
Longitudinal study (except cohorts) |
| Origine du recrutement des participants |
A selection of health care professionals An administrative base or a register |
| Le recrutement dans la base de données s'effectue dans le cadre d'une étude interventionnelle |
No |
| Informations complémentaires concernant la constitution de l'échantillon |
Selection of GP: A pre-selection via random drawing will be established using a CEGEDIM file of general practitioners. The general practitioners pre-selected through the random drawing will receive a mailing which will briefly present the objectives of the study and how it will unfold. It will include a postage-paid response card to be returned to the logistics center indicating whether or not the practitioner wants to participate in the study A telephone call to confirm participation will be made to the first 1000 general practitioners who have agreed Selection of pneumologists: A pre-selection via random drawing will be established using a CEGEDIM file of pneumologist/allergy doctors. The pre-selected pneumologists/allergy doctors will be contacted by telephone (brief presentation of the objectives and the unfolding of the study) in the order of the preselection until the number of pneumologists/allergy doctors accepting to participate reaches 500. The patients will be included after they have read the patient information letter |
| Objectif de la base de données | |
| Objectif principal | Describe in actual practice the level of control of asthma using the ACT questionnaire (Asthma Control Test) |
| Critères d'inclusion |
Male or female aged 18 years or older Patient having asthma diagnosed at least 12 months ago Patient informed of the objectives of the study and accepting the collection and the analysis of the data concerning him. |
| Type de population | |
| 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 concernée |
Sick population |
| Sexe |
Male Woman |
| Champ géographique |
National |
| Détail du champ géographique | France |
| Collecte | |
| Dates | |
| Année du premier recueil | 2006 |
| Année du dernier recueil | 2008 |
| Taille de la base de données | |
| Taille de la base de données (en nombre d'individus) |
[1000-10 000[ individuals |
| Détail du nombre d'individus | 2362 |
| Données | |
| Activité de la base |
Data collection completed |
| Type de données recueillies |
Clinical data Declarative data |
| Données cliniques, précisions |
Direct physical measures Medical registration |
| Données déclaratives, précisions |
Paper self-questionnaire |
| Existence d’une biothèque |
No |
| Paramètres de santé étudiés |
Health care consumption and services Quality of life/health perception |
| Consommation de soins, précisions |
Hospitalization Medical/paramedical consultation Medicines consumption |
| Modalités | |
| Mode de recueil des données | The physician will complete the medical questionnaire for inclusion and will give the inclusion self-questionnaire to the patient. During the 3-month inclusion period, the investigating physicians must collect in a data register patients who are not included in the cohort, that meet the eligibility criteria but who cannot or do not want to participate in the study. The patients included will be examined again at the next spontaneous consultation which will also be a follow-up visit within the framework of the study where a follow-up questionnaire will be completed by the investigator and a follow-up self-questionnaire will be given to the patient |
| Suivi des participants |
Yes |
| Détail du suivi | spontaneous consultation following the inclusion during which will be completed a medical follow-up questionnaire and a follow-up self-questionnaire |
| Appariement avec des sources administratives |
No |
| Valorisation et accès | |
| Valorisation et accès | |
| Accès | |
| Charte d'accès aux données (convention de mise à disposition, format de données et délais de mise à disposition) | Publications in progress |
| Accès aux données agrégées |
Access on specific project only |
| Accès aux données individuelles |
Access on specific project only |
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