Effectiveness of IMT/PEP Therapy in Group E COPD and Comparison of GOLD vs STAR Classifications

Bugra Kerget

Status: Completed

Conditions: Inspiratory Muscle Training; COPD

Treatments: Behavioral: Inspiratory Muscle Training / Positive Expiratory Pressure (IMT/PEP) Therapy

Study type: Observational

Funder types: Other

Identifiers

NCT07001462

B.30.2ATA.0.01.00/487

BAP-13001 (Atatürk University) (Other Grant/Funding Number)

Details and patient eligibility

About

This prospective study aims to evaluate the effects of inspiratory muscle training (IMT) combined with positive expiratory pressure (PEP) therapy on respiratory function, muscle strength, and symptom burden in patients with Group E chronic obstructive pulmonary disease (COPD). The primary objective is to compare the predictive value of the GOLD and STAR classification systems in identifying patients who respond better to IMT/PEP therapy. A total of 61 patients will receive standard COPD treatment along with IMT/PEP twice daily for 12 weeks. Pulmonary function tests, dyspnea scores, and 6-minute walk test results will be assessed at baseline, at 1 month, and at 3 months. Regression analysis will be used to determine the independent predictors of treatment response.

Enrollment: 61 patients

Sex: All

Ages: 40 to 80 years old

Volunteers: No Healthy Volunteers

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

Trial design

61 participants in 1 patient group

IMT/PEP Group

Description:

Patients with Group E chronic obstructive pulmonary disease (COPD) who received standardized pharmacological treatment combined with inspiratory muscle training and positive expiratory pressure (IMT/PEP) therapy. The intervention was administered using a dual-function device twice daily for 12 weeks.

Treatment:

Behavioral: Inspiratory Muscle Training / Positive Expiratory Pressure (IMT/PEP) Therapy