The goal of this single-site, parallel-group, double-blind, sham-controlled randomized control trial is to examine the effect of high-intensity inspiratory muscle strength training (IMST) on coronary blood flow assessed using positron emission tomography coronary perfusion imaging in patients with coronary artery disease (CAD). The main question it aims to answer are: • if high-intensity IMST will improve coronary blood flow in patients with CAD, which could be assessed using positron emission tomography coronary perfusion imaging. Participants will be asked to complete the 8-week high-intensity or low-intensity IMST. Researchers will compare high and low-intensity IMST groups to see if coronary blood flow increases after IMST.
Coronary artery disease (CAD) is a leading cause of morbidity and mortality. With the aging population, increasing number of patients with CAD has frailty and immobility. The health benefits of traditional aerobic exercise have been well-established; however, alternative exercise programs, such as inspiratory muscle training (IMST), may provide greater merits. IMST is a form of exercise that engages the diaphragm and accessory respiratory muscles to repeatedly inhale against resistance, which can be achieved in less time and widely applicable even for immobile or frail patients compared to conventional aerobic exercise. Since barriers to conventional exercise training include immobility, lack of time, and access to facilities, IMST may be a beneficial exercise form that can overcome those factors. A previous study has shown that high-intensity IMT can lower blood pressure and improved vascular endothelial function. Improvements in endothelial function of coronary arteries could improve coronary blood flow, leading to the improvement of anginal symptoms as well as quality of life. IMST might offer a widely applicable, feasible, time-efficient form of training for CAD patients. Our study will examine the preliminary efficacy of IMST on coronary blood flow in patients with CAD.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
40
Participants will use the POWERbreathe KHP2 inspiratory muscle training device. All participants will be assigned to perform 30 inspiratory maneuvers (5 sets of 6, 1-minute rest between sets), 6 days per week, for 6 weeks. Participants will be trained at 55% PIMAX during week 1, 65% PIMAX during week 2, and 75% PIMAX during weeks 3 to 6.
Participants will use the POWERbreathe KHP2 inspiratory muscle training device. All participants will be assigned to perform 30 inspiratory maneuvers (5 sets of 6, 1-minute rest between sets), 6 days per week, for 6 weeks. Participants will be trained at 15% PIMAX for 6 weeks.
University of Ottawa Heart Institute
Ottawa, Ontario, Canada
Global myocardial flow reserve
Change in global myocardial flow reserve on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Global stress myocardial blood flow
Change in global stress myocardial blood flow on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Global rest myocardial blood flow
Change in global rest myocardial blood flow on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Maximum myocardial flow reserve
Change in maximum myocardial flow reserve on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Maximum myocardial blood flow at rest and stress
Change in maximum myocardial blood flow at rest and stress on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Global coronary vascular resistance at stress and rest
Change in global coronary vascular resistance at stress and rest on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Maximum coronary vascular resistance at stress and rest
Change in maximum coronary vascular resistance at stress and rest on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Mean segmental (17-segment model) myocardial flow reserve
Change in mean segmental (17-segment model) myocardial flow reserve on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Mean segmental (17-segment model) myocardial blood flow at stress and rest
Change in mean segmental (17-segment model) myocardial blood flow at stress and rest on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Maximal segmental (17-segment model) myocardial blood flow at stress and rest
Change in maximal segmental (17-segment model) myocardial blood flow at stress and rest on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
Summed stress score, summed rest score, and summed difference score
Change in summed stress score, summed rest score, and summed difference score on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
% left ventricular ischemia
Change in % left ventricular ischemia on positron emission tomography coronary perfusion imaging before and after IMST
Time frame: Through study completion, an average of 8 weeks
General quality of life
Change in general Quality of life assessed using the EQ5D-5L
Time frame: Through study completion, an average of 8 weeks
Angina symptom
Change in angina symptom assessed using the Seattle angina Questionnaire
Time frame: Through study completion, an average of 8 weeks
Adherence of IMST program
The proportion of participants adhering to prescribed IMST sessions
Time frame: Through study completion, an average of 8 weeks
Respiratory Muscle Strength
Respiratory Muscle Strength assessed by % change in maximal inspiratory pressure
Time frame: Through study completion, an average of 8 weeks
Resting blood pressure
Resting blood pressure measured in a seated position after a 5-minute rest period using an automated blood pressure monitor.
Time frame: Through study completion, an average of 8 weeks
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