Coronary Artery Disease Clinical Trial
— BREATHEOfficial title:
The Efficacy of Inspiratory Muscle Strength Training on Coronary Blood Flow in Patients With Coronary Artery Disease
NCT number | NCT05632614 |
Other study ID # | 20220463-01H |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 8, 2023 |
Est. completion date | June 30, 2025 |
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.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | June 30, 2025 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion criteria: 1. =18 years of age; 2. Patients referred to PET at the University of Ottawa Heart Institute; 3. able to perform a respiratory exercise testing; and, 4. Patients with clinical stability, including no change in medications for the past one month. Exclusion criteria: 1. unstable angina or established diagnosis of severe valvular heart disease, hypertrophic obstructive cardiomyopathy, chronic obstructive pulmonary disease; 2. unable to follow training/breathing instructions; 3. unable to return for follow-up visit; 4. presence of any major non-cardiac problem that would adversely affect survival during the study in the opinion of the investigator; or, 5. unable to provide informed consent. |
Country | Name | City | State |
---|---|---|---|
Canada | University of Ottawa Heart Institute | Ottawa | Ontario |
Lead Sponsor | Collaborator |
---|---|
Ottawa Heart Institute Research Corporation |
Canada,
Arnett DK, Blumenthal RS, Albert MA, Buroker AB, Goldberger ZD, Hahn EJ, Himmelfarb CD, Khera A, Lloyd-Jones D, McEvoy JW, Michos ED, Miedema MD, Munoz D, Smith SC Jr, Virani SS, Williams KA Sr, Yeboah J, Ziaeian B. 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol. 2019 Sep 10;74(10):1376-1414. doi: 10.1016/j.jacc.2019.03.009. Epub 2019 Mar 17. Erratum In: J Am Coll Cardiol. 2019 Sep 10;74(10):1428-1429. J Am Coll Cardiol. 2020 Feb 25;75(7):840. — View Citation
Chiappa GR, Roseguini BT, Vieira PJ, Alves CN, Tavares A, Winkelmann ER, Ferlin EL, Stein R, Ribeiro JP. Inspiratory muscle training improves blood flow to resting and exercising limbs in patients with chronic heart failure. J Am Coll Cardiol. 2008 Apr 29;51(17):1663-71. doi: 10.1016/j.jacc.2007.12.045. — View Citation
Cipriano GF, Cipriano G Jr, Santos FV, Guntzel Chiappa AM, Pires L, Cahalin LP, Chiappa GR. Current insights of inspiratory muscle training on the cardiovascular system: a systematic review with meta-analysis. Integr Blood Press Control. 2019 May 20;12:1-11. doi: 10.2147/IBPC.S159386. eCollection 2019. — View Citation
Craighead DH, Heinbockel TC, Freeberg KA, Rossman MJ, Jackman RA, Jankowski LR, Hamilton MN, Ziemba BP, Reisz JA, D'Alessandro A, Brewster LM, DeSouza CA, You Z, Chonchol M, Bailey EF, Seals DR. Time-Efficient Inspiratory Muscle Strength Training Lowers Blood Pressure and Improves Endothelial Function, NO Bioavailability, and Oxidative Stress in Midlife/Older Adults With Above-Normal Blood Pressure. J Am Heart Assoc. 2021 Jul 6;10(13):e020980. doi: 10.1161/JAHA.121.020980. Epub 2021 Jun 29. — View Citation
Craighead DH, Heinbockel TC, Hamilton MN, Bailey EF, MacDonald MJ, Gibala MJ, Seals DR. Time-efficient physical training for enhancing cardiovascular function in midlife and older adults: promise and current research gaps. J Appl Physiol (1985). 2019 Nov 1;127(5):1427-1440. doi: 10.1152/japplphysiol.00381.2019. Epub 2019 Sep 26. — View Citation
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Lee IM, Shiroma EJ, Lobelo F, Puska P, Blair SN, Katzmarzyk PT; Lancet Physical Activity Series Working Group. Effect of physical inactivity on major non-communicable diseases worldwide: an analysis of burden of disease and life expectancy. Lancet. 2012 Jul 21;380(9838):219-29. doi: 10.1016/S0140-6736(12)61031-9. — View Citation
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Global myocardial flow reserve | Change in global myocardial flow reserve on positron emission tomography coronary perfusion imaging before and after IMST | Through study completion, an average of 8 weeks | |
Primary | Global stress myocardial blood flow | Change in global stress myocardial blood flow on positron emission tomography coronary perfusion imaging before and after IMST | Through study completion, an average of 8 weeks | |
Secondary | Global rest myocardial blood flow | Change in global rest myocardial blood flow on positron emission tomography coronary perfusion imaging before and after IMST | Through study completion, an average of 8 weeks | |
Secondary | Maximum myocardial flow reserve | Change in maximum myocardial flow reserve on positron emission tomography coronary perfusion imaging before and after IMST | Through study completion, an average of 8 weeks | |
Secondary | 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 | Through study completion, an average of 8 weeks | |
Secondary | 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 | Through study completion, an average of 8 weeks | |
Secondary | 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 | Through study completion, an average of 8 weeks | |
Secondary | 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 | Through study completion, an average of 8 weeks | |
Secondary | 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 | Through study completion, an average of 8 weeks | |
Secondary | 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 | Through study completion, an average of 8 weeks | |
Secondary | 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 | Through study completion, an average of 8 weeks | |
Secondary | % left ventricular ischemia | Change in % left ventricular ischemia on positron emission tomography coronary perfusion imaging before and after IMST | Through study completion, an average of 8 weeks | |
Secondary | General quality of life | Change in general Quality of life assessed using the EQ5D-5L | Through study completion, an average of 8 weeks | |
Secondary | Angina symptom | Change in angina symptom assessed using the Seattle angina Questionnaire | Through study completion, an average of 8 weeks | |
Secondary | Adherence of IMST program | The proportion of participants adhering to prescribed IMST sessions | Through study completion, an average of 8 weeks | |
Secondary | Respiratory Muscle Strength | Respiratory Muscle Strength assessed by % change in maximal inspiratory pressure | Through study completion, an average of 8 weeks | |
Secondary | Resting blood pressure | Resting blood pressure measured in a seated position after a 5-minute rest period using an automated blood pressure monitor. | Through study completion, an average of 8 weeks |
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