About this trial
This study investigates the effect of threshold inspiratory muscle training on diaphragm thickness and diaphragm excursion, measured using ultrasonography, in patients with stable chronic obstructive pulmonary disease (COPD).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with a COPD GOLD stage 2
Age 40-59 years
Maximal Inspiratory Pressure (MIP) value of less than 70 cmH₂O or below the lower limit of normal for their age and gender
Clinically stable for at least 4 weeks prior to the study
Disqualifiers
Patients with contraindications to Inspiratory Muscle Training or spirometry (e.g., recent thoracic or abdominal surgery, pneumothorax, or history of spontaneous pneumothorax).
Patients participating in other structured respiratory muscle training or pulmonary rehabilitation programs concurrently that could confound the results
Patients undergoing other therapies that may affect diaphragmatic muscle measurement results, such as electrical diaphragmatic stimulation
Trial design
Single group
Treatments tested in this trial
Threshold Inspiratory Muscle Training
Other interventionThreshold inspiratory muscle training performed using a threshold loading device to improve inspiratory muscle strength. Training is conducted once daily, five times per week for 6 weeks, with intensity starting at 30% and progressively increasing up to 50% of maximal inspiratory pressure (MIP) based on patient tolerance.
Philips Respironics Threshold IMT device
DeviceA threshold loading device used to provide inspiratory resistance during inspiratory muscle training
Treatment groups
Trial outcomes
Primary outcomes
Diaphragm Thickness (cm)
Diaphragm thickness reflects the structural characteristics of the diaphragm muscle and is measured at end-inspiration and end-expiration using ultrasonography. The values are expressed in centimeters (cm).
Diaphragm Excursion (cm)
Diaphragm excursion represents the vertical movement of the diaphragm during the respiratory cycle, reflecting diaphragmatic mobility and function. Measurements are obtained using ultrasonography and expressed in centimeters (cm).
Secondary outcomes
Forced Vital Capacity (FVC)
Forced Vital Capacity (FVC) is assessed using spirometry and measured in liters (L). It represents the total volume of air that can be forcibly exhaled after a full inhalation and reflects overall lung capacity.
Forced Expiratory Volume in one second (FEV1)
Forced Expiratory Volume in one second (FEV1) is measured using spirometry and expressed in liters (L). It represents the volume of air exhaled in the first second of a forced expiration.
Peak Expiratory Flow (PEF)
Peak Expiratory Flow (PEF) is measured using spirometry and expressed in liters per second (L/s). It reflects the maximum airflow achieved during forced expiration and indicates airway function.
Locations
Sponsors and contacts
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Universitas Padjadjaran
Lead sponsor
Dr. Hasan Sadikin General Hospital, Bandung, Indonesia
Collaborator
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