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Clinical Trials/NCT04481074
NCT04481074
Completed
N/A

Effects of Inspiratory Muscle Training in Inspiratory Muscle Endurance, Breathlessness, Inspiratory Muscle Strength, Functional Capacity and Quality of Life in Patients With Interstitial Lung Disease

Federal University of Minas Gerais2 sites in 1 country14 target enrollmentJuly 30, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Interstitial Fibrosis
Sponsor
Federal University of Minas Gerais
Enrollment
14
Locations
2
Primary Endpoint
Change in Breathlessness
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The aim of this study is to evaluate the effects of inspiratory muscle training program in inspiratory muscle endurance, breathlessness, inspiratory muscle strength, functional capacity and quality of life in patients with interstitial lung disease. Patients are evaluated before the inspiratory muscle training and after 8 weeks of training.

Detailed Description

Inspiratory Muscle Training has been described as an effective intervention and contribute to the improvement of inspiratory muscle function and breathlessness in patients with chronic lung disease. The aim of this study is to evaluate, the effects of inspiratory muscle endurance, breathlessness, inspiratory muscle strength, functional capacity and quality of life in patients with interstitial lung disease. It is a quasi-experimental study. Patients with interstitial lung disease are recruited from interstitial disease ambulatory. In each session patients performs two times 30 breaths with a minute rest between them. The load is set according with 50% of actual PImax, the Borg score should be between 4 and 6, otherwise the load will decrease (if Borg more than 6) or increase (if Borg less than 4). New PImax is measured weekly and the new load is defined following the same protocol for 8 weeks. Patients are evaluated before the inspiratory muscle training and after 8 weeks of training.

Registry
clinicaltrials.gov
Start Date
July 30, 2020
End Date
April 30, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Federal University of Minas Gerais
Responsible Party
Principal Investigator
Principal Investigator

Veronica Franco Parreira

Full Professor

Federal University of Minas Gerais

Eligibility Criteria

Inclusion Criteria

  • Clinical and radiological diagnosis of interstitial lung disease established by a pulmonologist;
  • Absence of clinical exacerbations of the disease in the four weeks prior to the initial data collection;
  • Present medical research council scale more than 2;
  • Absence of a associated or self reported cardiac, orthopedic and psychiatric diseases,
  • Not participating in pulmonary rehabilitation programs;
  • Do not use supplemental oxygen therapy while resting.

Exclusion Criteria

  • Inability of the participant to understand or perform the procedures proposed during the evaluations and training program.

Outcomes

Primary Outcomes

Change in Breathlessness

Time Frame: At baseline and after 8 weeks of training

Medical Research Council (1-5)

Change in Inspiratory muscle endurance

Time Frame: At baseline and after 8 weeks of training

Endurance time in seconds

Secondary Outcomes

  • Change in Inspiratory muscle strength(At baseline and after 8 weeks of training)
  • Change in Functional capacity(At baseline and after 8 weeks of training)
  • Change in Quality of life(At baseline and after 8 weeks of training)

Study Sites (2)

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