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Clinical Trials/NCT05353556
NCT05353556
Completed
Not Applicable

Effects of Home-based Inspiratory Muscle Training in Patients With Idiopathic Pulmonary Fibrosis

Dokuz Eylul University1 site in 1 country28 target enrollmentFebruary 21, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Idiopathic Pulmonary Fibrosis
Sponsor
Dokuz Eylul University
Enrollment
28
Locations
1
Primary Endpoint
Change in inspiratory muscle strength
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to investigate the effects of the home-based inspiratory muscle training program on lung functions, dyspnea, inspiratory muscle strength, functional capacity and quality of life in patients with idiopathic pulmonary fibrosis. Patients are evaluated before the inspiratory muscle training and after 8 weeks of training.

Detailed Description

The IMT protocol consisted of home-based high-intensity daily training - two cycles of 30 breaths with a 1-min rest between sets, twice a day for 8 weeks using an IMT Threshold device (Threshold IMT Philips® Respironics, Inc). The intensity of the training was set to 50% of each patient's maximal inspiratory pressure measured every week and was adjusted weekly based on the modified Borg scale from 4 to 6 regarding respiratory effort performed during the session. Patients are evaluated before the inspiratory muscle training and after 8 weeks of training.

Registry
clinicaltrials.gov
Start Date
February 21, 2022
End Date
May 30, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ridvan Aktan

Principal Investigator, PhD

Izmir University of Economics

Eligibility Criteria

Inclusion Criteria

  • Diagnosing Idiopathic Pulmonary Fibrosis by a pulmonologist;
  • Aged between 40 and 75 years;
  • Volunteering to research;
  • Stable clinical condition (same medication routine and/or no acute exacerbation in the last for the last 4 weeks).

Exclusion Criteria

  • Inability of the participant to understand or perform the procedures proposed during the evaluations or training program.
  • Participating in any pulmonary rehabilitation programs;
  • A previous pneumonectomy or lobectomy operation;
  • Pneumonia in the last 4 weeks;
  • Any pulmonary infection during the study;
  • Requirement for supplemental oxygen therapy while resting.
  • Having Covid-19 disease (during the study or in the past)
  • Orthopaedic or neurological conditions affecting the ability to independent walking

Outcomes

Primary Outcomes

Change in inspiratory muscle strength

Time Frame: 8 weeks

MIP

Secondary Outcomes

  • Change in Dyspnea(8 weeks)
  • Change in percentages of forced vital capacity(8 weeks)
  • Change in diffusing capacity of the lung for carbon monoxide(8 weeks)
  • Change in Functional capacity(8 weeks)
  • Change in percentages of forced expiratory volume in one second(8 weeks)

Study Sites (1)

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