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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT00932711
Other study ID # 4140-B
Secondary ID
Status Enrolling by invitation
Phase N/A
First received July 2, 2009
Last updated July 2, 2009
Start date July 2009
Est. completion date July 2011

Study information

Verified date June 2009
Source Minneapolis Veterans Affairs Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if educational intervention is effective in reducing exacerbations of chronic obstructive pulmonary disease in patients with low-risk disease.


Description:

There is growing evidence about the effectiveness of case management in preventing adverse events in patients with high-risk chronic obstructive pulmonary disease(COPD). But the majority of COPD patients belong to the low-risk category. We propose that a less intense educational intervention will have a similar beneficial effect in reducing hospital admissions and emergency department (ED) visits in this larger group of low-risk COPD patients.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 4000
Est. completion date July 2011
Est. primary completion date June 2010
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria: Spirometrically confirmed COPD in VISN23 registry. FEV1/FVC <70%.

Exclusion Criteria:Hospital admissions or ED visits in the VISN23 disease registry for COPD within last one year

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Educational brochures
A locally developed educational brochure containing information about smoking cessation, influenza and pneumococcal vaccination, regular exercise, compliance with prescribed COPD therapy and recognition of symptoms, along with a goal setting questionnaire

Locations

Country Name City State
United States Minneapolis VA Medical Center Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
VA Office of Research and Development

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Combined frequency of admissions and ED visits for COPD over 1 year. One year No
Secondary Patient knowledge of COPD will be compared. 1 year No
Secondary Use of respiratory medications will be compared 1 year No
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