Evaluation of the Frequency of Limitation of Activity in Patients With Persistent Asthma (ASMAVIE)
This study has been completed.
Sponsor:
AstraZeneca
Information provided by (Responsible Party):
AstraZeneca
ClinicalTrials.gov Identifier:
NCT01078688
First received: February 25, 2010
Last updated: January 28, 2013
Last verified: January 2013
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Purpose
Evaluation of the frequency of limitation of activity, depending on gender and age-group, in patients with persistent asthma consulting a general practitioner
| Condition |
|---|
|
Persistent Asthma |
| Study Type: | Observational |
| Study Design: | 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 |
Resource links provided by NLM:
Further study details as provided by AstraZeneca:
Primary Outcome Measures:
- To describe the frequency of limitations of activities in patients with persistent asthma depending on gender and age-group. [ Time Frame: Last 3 months / once ] [ Designated as safety issue: No ]
- 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. [ Time Frame: Once during only visit ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- 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 [ Time Frame: Once during only visit ] [ Designated as safety issue: No ]
- 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 [ Time Frame: Once during only visit ] [ Designated as safety issue: No ]
- To describe the main characteristics and initial management for all patients of the survey [ Time Frame: Once during only visit ] [ Designated as safety issue: No ]
| Enrollment: | 1942 |
| Study Start Date: | March 2010 |
| Study Completion Date: | October 2010 |
| Primary Completion Date: | October 2010 (Final data collection date for primary outcome measure) |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Study Population
First 3 consecutive patients with persistent asthma seen by general practitioner receiving long-term maintenance treatment with inhaled steroids
Criteria
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
Please refer to this study by its ClinicalTrials.gov identifier: NCT01078688
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Sponsors and Collaborators
AstraZeneca
Investigators
| Study Director: | Pascal Piedbois | AstraZeneca |
More Information
No publications provided
| Responsible Party: | AstraZeneca |
| ClinicalTrials.gov Identifier: | NCT01078688 History of Changes |
| Other Study ID Numbers: | NIS-RFR-DUM-2009/2 |
| Study First Received: | February 25, 2010 |
| Last Updated: | January 28, 2013 |
| Health Authority: | France: French Data Protection Authority |
Keywords provided by AstraZeneca:
|
Limitations of activities persistent asthma general practitioner frequency of limitations of activities depending on gender and age-group |
Additional relevant MeSH terms:
|
Asthma Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases |
Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |
ClinicalTrials.gov processed this record on May 16, 2013