ASMAVIE: Evaluation of the Frequency of Limitation of Activity in Patients With Persistent Asthma

Sponsor
AstraZeneca (Industry)
Overall Status
Completed
CT.gov ID
NCT01078688
Collaborator
(none)
1,942
728
7
2.7
0.4

Study Details

Study Description

Brief Summary

Evaluation of the frequency of limitation of activity, depending on gender and age-group, in patients with persistent asthma consulting a general practitioner

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    1942 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Evaluation of the Frequency of Limitation of Activity, Depending on Gender and Age-group, in Patients With Persistent Asthma Consulting a General Practitioner
    Study Start Date :
    Mar 1, 2010
    Actual Primary Completion Date :
    Oct 1, 2010
    Actual Study Completion Date :
    Oct 1, 2010

    Outcome Measures

    Primary Outcome Measures

    1. To describe the frequency of limitations of activities in patients with persistent asthma depending on gender and age-group. [Last 3 months / once]

    2. To describe, depending on gender and age-group, the nature of the activities limited, the degree of limitation and the impact on the patient's daily life. [Once during only visit]

    Secondary Outcome Measures

    1. To describe the nature of the activities limited, the degree of limitation and the impact on the patient's daily life according to the level of asthma control [Once during only visit]

    2. To describe, depending on gender and age-group, the activities that need to be specifically investigated in routine clinical practice due to their greater impact on the patient's quality of life, and which could indicate poorly controlled asthma [Once during only visit]

    3. To describe the main characteristics and initial management for all patients of the survey [Once during only visit]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • persistent asthma receiving long-term maintenance treatment with inhaled steroids (alone or in combination with other drugs)
    Exclusion Criteria:
    • Patients with a diagnosis of COPD

    Contacts and Locations

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    691 Research Site Velleron France
    692 Research Site Venarey Les Laumes France
    693 Research Site Vendeuil France
    694 Research Site Vendome France
    695 Research Site Verfeil France
    696 Research Site Vernouillet France
    697 Research Site Verquieres France
    698 Research Site Vertus France
    699 Research Site Vervins France
    700 Research Site VIF France
    701 Research Site Vigneux Sur Seine France
    702 Research Site Vihiers France
    703 Research Site Ville Di Pietrabugno France
    704 Research Site Villefontaine France
    705 Research Site Villefranche de Rouergue France
    706 Research Site Villefranque France
    707 Research Site Villejuif France
    708 Research Site Villemeux Sur Eure France
    709 Research Site Villemomble France
    710 Research Site Villeneuve Tolosane France
    711 Research Site Villepreux France
    712 Research Site Villers Bocage France
    713 Research Site Villers Bretonneux France
    714 Research Site Villette D Anthon France
    715 Research Site Villeurbanne France
    716 Research Site Villiers Sur Marne France
    717 Research Site Vinay France
    718 Research Site Vincennes France
    719 Research Site Vitrolles France
    720 Research Site Vitteaux France
    721 Research Site Vivy France
    722 Research Site Voisins Le Bretonneux France
    723 Research Site Voujeaucourt France
    724 Research Site Wattrelos France
    725 Research Site Waziers France
    726 Research Site Wignehies France
    727 Research Site Wittelsheim France
    728 Research Site Yerville France

    Sponsors and Collaborators

    • AstraZeneca

    Investigators

    • Study Director: Pascal Piedbois, AstraZeneca

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    AstraZeneca
    ClinicalTrials.gov Identifier:
    NCT01078688
    Other Study ID Numbers:
    • NIS-RFR-DUM-2009/2
    First Posted:
    Mar 2, 2010
    Last Update Posted:
    Jan 29, 2013
    Last Verified:
    Jan 1, 2013

    Study Results

    No Results Posted as of Jan 29, 2013