Skip to main content
Clinical Trials/NCT02179983
NCT02179983
Terminated
Not Applicable

A Randomized Controlled Trial of Pulmonary Rehabilitation After Exacerbations of Bronchiectasis

NHS Tayside1 site in 1 country48 target enrollmentJune 2014
ConditionsBronchiectasis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bronchiectasis
Sponsor
NHS Tayside
Enrollment
48
Locations
1
Primary Endpoint
6 minute walk distance
Status
Terminated
Last Updated
5 years ago

Overview

Brief Summary

Pulmonary rehabilitation is well established as a treatment in COPD. After exacerbations of COPD, rehabilitation is associated with reduced frequency of exacerbations and improved exercise capacity. No data are available in bronchiectasis.

This study will randomly assign patients with bronchiectasis exacerbations to pulmonary rehabilitation or standard care. The hypothesis is that exercise capacity will be improved by pulmonary rehabilitation at 8 weeks.

Detailed Description

Background: Pulmonary rehabilitation is an effective treatment after exacerbations of COPD to prevent future exacerbations and to improve breathlessness and quality of life. Its effectiveness after exacerbations of bronchiectasis has never been demonstrated. Aims: To determine if a 6 week course of pulmonary rehabilitation improves exercise capacity at 8 weeks after exacerbation. Study Design: Randomised controlled trial. Methods: The study will take place in NHS Tayside. 40 patients with a history of bronchiectasis confirmed by HRCT will be included. Patients will be monitored using diary cards for exacerbations. At the onset of an exacerbation patients will be treated with a standard 14 day course of antibiotic therapy and randomised to one of two arms: Pulmonary rehabilitation or standard care. Patients randomised to pulmonary rehabilitation will undergo a 6 week course of supervised pulmonary rehabilitation. Patients will undergo study assessments (6-minute walk test, Quality of life questionnaires, pulmonary function tests (FEV1, FVC, FEF 25-75), symptoms recorded by symptom diaries and sputum microbiology).Assessments will be performed at the start and end of exacerbations, at 6-8 weeks post exacerbation (after completion of pulmonary rehabilitation in patients randomised to rehabilitation) and at 12 weeks. Outcome: The primary outcome is 6 minute walk distance at 8 week post exacerbation Expected Conclusion: We will determine the effectiveness of pulmonary rehabilitation after exacerbations of bronchiectasis.

Registry
clinicaltrials.gov
Start Date
June 2014
End Date
June 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Bronchiectasis confirmed on High Resolution CT scan Clinical Bronchiectasis confirmed by a respiratory physician. Documented exacerbation within the last year. Independently mobile - i.e. able to undertake pulmonary rehabilitation

Exclusion Criteria

  • Inability to give informed consent to participate
  • Age \<18 years
  • Primary diagnosis of Chronic Obstructive Pulmonary Disease
  • Significant comorbidity that would limit the ability to undertake pulmonary rehabilitation - i.e. Cerebrovascular, cardiovascular or musculoskeletal disease.
  • Cystic Fibrosis
  • Aortic aneurysm
  • Recent myocardial infarction (within previous year)or unstable angina

Outcomes

Primary Outcomes

6 minute walk distance

Time Frame: 8 weeks post exacerbation

Secondary Outcomes

  • The Quality of life(8 weeks and 12 weeks)
  • Sputum microbiology(8 weeks and 12 weeks)
  • Time to next exacerbation(6 months)
  • Pulmonary function tests(8 weeks and 12 weeks)
  • Respiratory symptoms(8 weeks and 12 weeks)
  • 6 minute walk distance(12 weeks)

Study Sites (1)

Loading locations...

Similar Trials