COPD, Inspiratory Muscle Training
Conditions
Keywords
COPD, inspiratory muscle training, pulmonary rehabilitation, GOLD, STAR
Brief summary
Background: Inspiratory muscle training combined with positive expiratory pressure (IMT/PEP) may improve outcomes in chronic obstructive pulmonary disease (COPD), but evidence in exacerbation-prone (Group E) disease is limited. This study is designed to evaluate the effects of IMT/PEP on pulmonary function, respiratory muscle strength, exercise capacity, and dyspnea in stable Group E COPD. Methods : This prospective randomized controlled trial will enroll 62 patients with stable Group E COPD between June 2023 and September 2024. Participants will be randomized to receive IMT/PEP plus standard care or standard care alone. Pulmonary function tests, maximal inspiratory pressure (MIP), maximal expiratory pressure (MEP), six-minute walk test (6MWT), oxygen saturation (SO₂), and dyspnea scales (mMRC, CAT, MBS, VAS) will be assessed at baseline, 1 month, and 3 months.
Interventions
BEHAVIORALInspiratory Muscle Training / Positive Expiratory Pressure (IMT/PEP) Therapy
IMT/PEP therapy was administered using a dual-function device (BİO Breathe, Korea) designed to provide both inspiratory muscle resistance and positive expiratory pressure. Patients performed the therapy for 15 minutes, twice daily, over a 12-week period, in addition to standard pharmacological treatment. Pressure levels were individually adjusted between 5-40 cmH₂O based on patient capacity.
Sponsors
Bugra Kerget
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
Age ≥ 40 years Diagnosis of Group E COPD according to GOLD 2023 criteria Post-bronchodilator FEV₁/FVC \< 0.70 and FEV₁ \< 50% predicted mMRC score ≥ 2 or CAT score ≥ 10 History of ≥2 exacerbations or ≥1 hospitalization in the past year Stable clinical condition (no exacerbation in the past 2 weeks) Ability and willingness to perform IMT/PEP therapy Provided written informed consent
Exclusion criteria
Acute exacerbation of COPD at time of enrollment Contraindications to pulmonary function testing or 6-minute walk test (e.g., recent myocardial infarction, unstable angina) Inability to perform inspiratory or expiratory maneuvers reliably (e.g., due to cognitive or neuromuscular disorders) Significant orofacial muscle weakness unresponsive to modified mouthpiece Participation in another interventional study within the past 3 months Nonadherence to COPD treatment plan Any condition deemed by investigators to interfere with study participation
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Maximal Inspiratory Pressure (MIP) After 12 Weeks of IMT/PEP Therapy | Baseline and Week 12 | Maximal inspiratory pressure (MIP) was measured at baseline and after 12 weeks using a digital manometer at residual volume (RV) to evaluate the effect of IMT/PEP therapy on inspiratory muscle strength. |
| Change in Residual Volume (RV) After 12 Weeks of IMT/PEP Therapy | Baseline and Week 12 | Residual volume (RV) was obtained through whole-body plethysmography at baseline and after 12 weeks to assess the impact of IMT/PEP therapy on pulmonary hyperinflation. |
Countries
Turkey (Türkiye)
Outcome results
None listed