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Asthma Patient Survey Study to Assess Asthma Effect and Medication in Finland
This study has been completed.
First Received: May 19, 2008   Last Updated: November 4, 2009   History of Changes
Sponsor: AstraZeneca
Information provided by: AstraZeneca
ClinicalTrials.gov Identifier: NCT00681382
  Purpose

This study was aimed at clarifying how the asthma medication is used in practice and how asthma affects everyday life. Total of 106 GPs were asked to recruit patients using inhaled steroid as maintenance treatment for asthma to take part in a telephone survey. Altogether 142 patients were interviewed.


Condition
Asthma

Study Type: Observational
Study Design: Case-Only, Cross-Sectional
Official Title: INSPIRE Asthma Patient Survey to Clarify the Use of Asthma Medication and Effects of Asthma in Everyday Life in Finland

Resource links provided by NLM:


Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • Patients perceptions about treatment of asthma, asthma medication and what are the most common triggers that cause exacerbations. [ Time Frame: Single occasion ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • How patients react to the first signs of worsening of asthma i.e. how they use asthma medication during stable phase and asthma exacerbation [ Time Frame: Single occasion ] [ Designated as safety issue: No ]
  • How asthma affects everyday life [ Time Frame: Single occasion ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Enrollment: 142
Study Start Date: October 2006
Primary Completion Date: April 2007 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
Asthma patients using inhaled steroids as maintenance treatment

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Primary care clinic

Criteria

Inclusion Criteria:

  • Diagnosed persistent asthma
  • regular use of inhaled steroids and concomitant medication

Exclusion Criteria:

  • never been diagnosed COPD
  • seasonal asthma
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00681382

Sponsors and Collaborators
AstraZeneca
Investigators
Study Director: Airi Puhakka AstraZeneca Finland
Principal Investigator: Jouni Hedman South Karelia Central Hospital, Finland
  More Information

No publications provided

Responsible Party: AstraZeneca ( Klaus Tamminen - MC Medical Director )
Study ID Numbers: NIS-RFI-SYM-2006/1
Study First Received: May 19, 2008
Last Updated: November 4, 2009
ClinicalTrials.gov Identifier: NCT00681382     History of Changes
Health Authority: Finland: Ethics Committee

Keywords provided by AstraZeneca:
Asthma
use of asthma medication
asthma control
telephone survey
patient's perception

Additional relevant MeSH terms:
Hypersensitivity
Lung Diseases, Obstructive
Immune System Diseases
Respiratory Tract Diseases
Bronchial Diseases
Lung Diseases
Hypersensitivity, Immediate
Asthma
Respiratory Hypersensitivity

ClinicalTrials.gov processed this record on November 30, 2009