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Effect of Inspiratory Muscle Training on Exercise Performance and Quality of Life in Patients With Chronic Obstructive Pulmonary Disease

Effect of Inspiratory Muscle Training on Exercise Performance and Quality of Life in Patients With Chronic Obstructive Pulmonary Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02257463
Enrollment
60
Registered
2014-10-06
Start date
2011-10-31
Completion date
2014-04-30
Last updated
2015-04-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

COPD, inspiratory muscle training, dyspnea, Quality of Life

Brief summary

The aim is to study effectiveness of inspiratory muscle training as a part of exercise training in patients with Chronic Obstructive Pulmonary Disease (COPD) and if it adds to general exercise training program in regard to respiratory muscle strength, dyspnea, exercise performance and quality of life.

Interventions

DRUGtheophylline, long acting bronchodilators (LABD) or combined LABD and inhaled steroids according to GOLD recommendations
OTHERperipheral muscles exercise training
DEVICEinspiratory muscle training

Patients started breathing at a resistance that required generation of 30% of their PImax for one week. The load was then increased incrementally, 5-10%, to reach generation of 60% of their PImax at the end of the first month. Specific IMT was then continued at 60% of their PImax adjusted weekly to the new PImax achieved.

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
45 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Exsmokers * Low PImax compared to reference values \[lower limits of normal: 80 cmH2O for patients less than or equal 54 years old; 71 cmH2O for patients' age between 55-64 years; and 65 cmH2O for patients 65 years old \]. * Stable patients without history of exacerbation or hospitalization four weeks before starting the study.

Exclusion criteria

* Lack of motivation and compliance. * Patients with significant reversibility following bronchodilation defined as an increase in FEV1 of more than 12% and 200 ml from the pre-bronchodilator value * Unstable cardiac disease \[severe heart failure, dangerous dysrhythmias, recent myocardial infarction or unstable angina (within 4 weeks)\]. * Uncontrolled hypertension * Recent pneumothorax (within 6 weeks) * Recent abdominal or thoracic surgery (within 6 weeks) * Known progressive neuromuscular disorders * Recent gastrointestinal bleeding (within 4 weeks) * Current smokers * Active cancer * Patients with advanced liver diseases, or renal impairment. * Known connective tissue diseases * Significant endocrinal abnormalities

Design outcomes

Primary

MeasureTime frameDescription
changes in respiratory muscle strengthafter 4 weeks and after 8 weeks of studymaximal inspiratory pressure, maximal expiratory pressure
changes in perception of dyspneaafter 4 weeks and after 8 weeks of studymodified Medical Research Council and modified Borg category scale
changes in exercise performanceafter 4 weeks and after 8 weeks of study6-min walk test
changes in quality of lifeafter 4 weeks and after 8 weeks of studyBODE index, St. George's Respiratory Questionnaire for COPD patients (SGRQ-C)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026