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Clinical Trials/NCT02656992
NCT02656992
Completed
Not Applicable

Effects of High Intensity Inspiratory Muscle Training on Exercise Capacity in Patients With Bronchiectasis

Hacettepe University1 site in 1 country45 target enrollmentSeptember 2014
ConditionsBronchiectasis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bronchiectasis
Sponsor
Hacettepe University
Enrollment
45
Locations
1
Primary Endpoint
Exercise capacity using incremental shuttle walk test and 6-minute walk test
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Reduced exercise tolerance is commonly reported in patients with bronchiectasis. The purpose of this study is to evaluate the effects of high-intensity inspiratory muscle training (High-IMT) and sham High-IMT (control) on exercise capacity, respiratory muscle function (strength and endurance) and health related quality of life in patients with bronchiectasis.

Detailed Description

Bronchiectasis often demonstrates decreased exercise tolerance, marked dyspnea and fatigue. The causes are multifactorial and include altered pulmonary mechanics, inefficient gas exchange, decreased muscle mass, and psychological status, which all lead to a progressive detraining effect. Essentially both the pathology and the functional manifestations of bronchiectasis increase the demand for inspiratory muscle work and that contribute to dyspnea and exercise limitation. In recent studies reduced strength of respiratory muscles are investigated in bronchiectasis and can be contribute the exercise limitation. Additionally IMT has shown to improve respiratory muscle function, exercise tolerance and dyspnea in patients with bronchiectasis. Despite this, the number of studies are inadequate and so the optimal training protocol remains still to be defined. In this study the researchers want to investigate the effects of high-intensity inspiratory muscle training in functional results in patients with bronchiectasis.

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

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ozge OZER

Principal Investigator

Hacettepe University

Eligibility Criteria

Inclusion Criteria

  • diagnosis of bronchiectasis with high resolution computed tomography
  • being 18-65 years of age
  • being able to walk and co-operate

Exclusion Criteria

  • acute exacerbation or change in drugs or usage of antibiotics in last 3 weeks
  • neurological disease, severe orthopaedic problem or advanced heart failure

Outcomes

Primary Outcomes

Exercise capacity using incremental shuttle walk test and 6-minute walk test

Time Frame: Baseline to 8 weeks

* The incremental shuttle walk test will be performed in an enclosed corridor. Patients are required to walk back and forth, turning around two cones placed 9 meters apart making the shuttle distance 10 meters long. Patients will follow the rhythm dictated by the audio signal. * 6-minute walk test will be performed in a long, straight, enclosed corridor 30 meters in length. Patients are required to walk in their walking speed with standardised instructions. The distance walked by subjects during 6 minutes will be recorded.

Secondary Outcomes

  • Health related quality of life is assessed with Leicester Cough Questionnaire(Baseline to 8 weeks)
  • Dyspnea severity is assessed with The Modified Medical Research Council Dyspnea Scale (MMRC)(Baseline to 8 weeks)
  • Fatigue severity is assessed with Fatigue Severity Index(Baseline to 8 weeks)
  • Respiratory muscle strength(Baseline to 8 weeks)
  • Respiratory muscle endurance(Baseline to 8 weeks)
  • Severity of disease is assessed with Bronchiectasis Severity Index(Baseline to 8 weeks)

Study Sites (1)

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