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Clinical Trials/NCT01175265
NCT01175265
Completed
Phase 1

Effects of Breathing Retraining on Pulmonary Function, Exercise Capacity, Quality of Life and Cardiac Autonomic Function in Patients With COPD

University Hospital, Essen1 site in 1 country40 target enrollmentNovember 2008

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
University Hospital, Essen
Enrollment
40
Locations
1
Primary Endpoint
cardiopulmonary exercise capacity
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

Conventional pulmonary rehabilitation programs improve exercise tolerance, peripheral muscle strength, and health related quality of live but not pulmonary function in patients with chronic obstructive pulmonary disease (COPD). The role of breathing retraining techniques in the rehabilitation of patients with COPD remains unclear. The hypothesis to be tested in this study is that pulmonary function, cardio-pulmonary exercise capacity, health related quality of life and cardiac autonomic modulation of patients with COPD who undergo pulmonary rehabilitation plus breathing retraining will be better than that of patients undergoing a conventional pulmonary rehabilitation.

Detailed Description

To address this uncertainty, we performed a randomized controlled trial to assess the effects of a 4-week rehabilitation program including breathing retraining on pulmonary function (PFT), cardio-pulmonary exercise capacity (CPET), health related quality of life (HRQL) and cardiac autonomic modulation (CAM). A randomized controlled trial comparing the effects of a conventional 4-week pulmonary rehabilitation program with those of a 4-week pulmonary rehabilitation program plus breathing retraining on pulmonary function (FEV1), cardiopulmonary exercise capacity (6-minute walking distance, 6MWD), health related quality of life (chronic respiratory questionnaire, CRQ) and cardiac autonomic function (rMSSD) was performed.

Registry
clinicaltrials.gov
Start Date
November 2008
End Date
April 2010
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Essen

Eligibility Criteria

Inclusion Criteria

  • Clinically stable patients with COPD (GOLD-classification I-IV)

Exclusion Criteria

  • Patients with clinical signs of COPD exacerbation
  • Cardiac arrhythmia
  • Coronary artery disease
  • Primary pulmonary vascular disease
  • Oxygen desaturation to less than 80% during exercise on room air

Outcomes

Primary Outcomes

cardiopulmonary exercise capacity

6-minute walking distance, 6MWD

Secondary Outcomes

  • pulmonary function
  • quality of life
  • autonomic function

Study Sites (1)

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