Inspiratory Muscle Training in COPD

COPD Clinical Trial

Official title:

Inspiratory Muscle Strength and Endurance Training in Veterans With COPD

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03438019
• Other study ID #: 1160788-1
• Status: Recruiting
• Phase: N/A
• Start date: June 18, 2018
• Est. completion date: July 31, 2019

Study information

• Verified date: July 2018
• Source: Miami VA Healthcare System
• Contact: Michael A Campos, MD
• Phone: 3055757000
• Email: MCampos1[@]med.miami.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This proposal aims at evaluating an inspiratory muscle training (IMT) method not previously tested in COPD called the Test of Incremental Respiratory Endurance (TIRE). As a training method, TIRE promises to provide further benefits over standard IMT because it allows the user to adjust training loads as progress is made, adjusts the training based on day-to-day variations commonly noted in COPD, and provides a graphic representation of the inspiratory effort throughout all inspiration with real-time biofeedback in order to "coach" the user in performing the exercises. The TIRE device can also be used as an assessment tool, not only to measure the commonly used measure of inspiratory muscle strength Maximal Inspiratory Pressure (MIP), but also measuring the MIP variation generated throughout a maximal sustained inspiration. In this way, TIRE integrates MIP over the inspiratory duration (ID), providing a novel derivative measure called the sustained maximal inspiratory pressure or SMIP, that is likely a better surrogate of inspiratory muscle performance in COPD based upon preliminary data. The main goal of this trial is to fully evaluate the utility of TIRE as an IMT method in veterans with COPD. The investigators hypothesize that as a stand-alone therapy, TIRE training is superior to standard IMT in improving inspiratory muscle strength and endurance and in improving COPD-related clinical outcomes.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 36
• Est. completion date: July 31, 2019
• Est. primary completion date: July 1, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years and older

Eligibility

Inclusion Criteria:

• Male or female aged > 40 years with a confirmed diagnosis of COPD by a pulmonologist (presence of risk factors and airflow obstruction) and evidence of inspiratory muscle weakness as defined by the latest American Thoracic Society / European Respiratory Society statement on respiratory muscle training.

Exclusion Criteria:

• Refusal to participate in the study, subjects actively undergoing pulmonary rehabilitation, inability to perform the required maneuvers (i.e. patients with cerebrovascular accident or tracheostomy), subjects not in their stable state (i.e. having an acute exacerbation or within 4 weeks of having one) or presence of important comorbidities that may confound the interpretation of TIRE measures (i.e. decompensated heart failure, diaphragmatic paralysis, prior lung surgery, active cancer treatment, etc.). There will be no involvement of vulnerable populations.

Related Conditions & MeSH terms

• COPD
• Respiratory Aspiration

Intervention

Device:
• PrO2
The PrO2 device is linked to a tablet via Bluetooth and provides the user with a graphic representation of their inspiratory effort throughout all of inspiration and real-time biofeedback. This device incorporates a standard 2mm leak to avoid glottal closure during maximal inspiration. The PrO2 provides measures of MIP (cmH2O), SMIP (PTU) and ID (seconds).
• Threshold Inspiratory Muscle Trainer
The Threshold incorporates a flow-independent one-way valve to ensure consistent resistance and features an adjustable specific pressure setting to be set based on MIP values of each subject.

Locations

Country	Name	City	State
United States	Bruce W Carter VAMC	Miami	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Miami VA Healthcare System

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Six-minute Walk Test (6MWT)	Sub-maximal exercise test used to assess aerobic capacity and endurance. The best distance covered over a time of 6 minutes is recorded in metres.	Change from baseline to 8 weeks.
Other	St.George's Respiratory Questionnaire (SGRQ)	The SGRQ is a 50-item questionnaire developed to measure health status (quality of life) in patients with diseases of airways obstruction. Scores range from 0 to 100, with higher scores indicating more limitations.	Change from baseline to 8 weeks.
Other	Modified Medical Research Council (mMRC) Dyspnea Scale	This scale ranges from zero to four, with higher scores indicating a greater degree of breathlessness.	Change from baseline to 8 weeks.
Other	COPD Assessment Test (CAT)	This instrument that can quantify the impact of COPD on the patient's health. The CAT has a scoring range of 0-40. Higher scores denote a more severe impact of COPD.	Change from baseline to 8 weeks.
Other	Fat Free Mass Index (FFMI)	FFMI is calculated using the following formula: FFMI = (Lean Mass / 2.2) / ((Height in feet * 12.0) * 0.0254) squared. A person is said to be in the Average Norms of Muscle Mass Interpretation when his FFMI in pounds is between 18 and 19.	Change from baseline to 8 weeks.
Other	Short Performance Physical Battery (SPPB)	The SPPB is a group of measures that combines the results of the gait speed, chair stand and balance tests. The scores range from 0 (worst performance) to 12 (best performance).	Change from baseline to 8 weeks.
Primary	Sustained Maximal Inspiratory Pressure (SMIP)	SMIP is obtained from a maximal sustained inspiratory effort performed through the TIRE method using the PrO2 device. SMIP is documented in pressure time units (PTU) and represents the area under the curve generated from the start to the end of inspiration, from residual volume to total lung capacity.	Change from baseline to 8 weeks.
Secondary	Maximal Inspiratory Pressure (MIP)	MIP is obtained from a maximal inspiratory effort from residual volume using the TIRE software and recorded in centimeters of water.	Change from baseline to 8 weeks.
Secondary	Inspiratory Duration (ID)	ID is obtained from a maximal and sustained inspiratory effort using the TIRE software and recorded in seconds.	Change from baseline to 8 weeks.