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Blood Flow Reserve: Effects After Training With Heavy Inspiratory Exercises (BREATHE)

Primary Purpose

Coronary Artery Disease

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
High-intensity IMST
Low-intensity IMST
Sponsored by
Ottawa Heart Institute Research Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring inspiratory muscle strength training, coronary artery disease, positron emission tomography, myocardial blood flow

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria: ≥18 years of age; Patients referred to PET at the University of Ottawa Heart Institute; able to perform a respiratory exercise testing; and, Patients with clinical stability, including no change in medications for the past one month. Exclusion criteria: unstable angina or established diagnosis of severe valvular heart disease, hypertrophic obstructive cardiomyopathy, chronic obstructive pulmonary disease; unable to follow training/breathing instructions; unable to return for follow-up visit; presence of any major non-cardiac problem that would adversely affect survival during the study in the opinion of the investigator; or, unable to provide informed consent.

Sites / Locations

  • University of Ottawa Heart InstituteRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

High-intensity IMST

Low-intensity IMST

Arm Description

Participants who will be trained with high-intensity IMST

Participants who will be trained with low-intensity IMST

Outcomes

Primary Outcome Measures

Global myocardial flow reserve
Change in global myocardial flow reserve on positron emission tomography coronary perfusion imaging before and after IMST
Global stress myocardial blood flow
Change in global stress myocardial blood flow on positron emission tomography coronary perfusion imaging before and after IMST

Secondary Outcome Measures

Global rest myocardial blood flow
Change in global rest myocardial blood flow on positron emission tomography coronary perfusion imaging before and after IMST
Maximum myocardial flow reserve
Change in maximum myocardial flow reserve on positron emission tomography coronary perfusion imaging before and after IMST
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
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
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
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
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
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
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
% left ventricular ischemia
Change in % left ventricular ischemia on positron emission tomography coronary perfusion imaging before and after IMST
General quality of life
Change in general Quality of life assessed using the EQ5D-5L
Angina symptom
Change in angina symptom assessed using the Seattle angina Questionnaire
Adherence of IMST program
The proportion of participants adhering to prescribed IMST sessions
Respiratory Muscle Strength
Respiratory Muscle Strength assessed by % change in maximal inspiratory pressure
Resting blood pressure
Resting blood pressure measured in a seated position after a 5-minute rest period using an automated blood pressure monitor.

Full Information

First Posted
October 12, 2022
Last Updated
July 31, 2023
Sponsor
Ottawa Heart Institute Research Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT05632614
Brief Title
Blood Flow Reserve: Effects After Training With Heavy Inspiratory Exercises
Acronym
BREATHE
Official Title
The Efficacy of Inspiratory Muscle Strength Training on Coronary Blood Flow in Patients With Coronary Artery Disease
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 8, 2023 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
February 28, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Heart Institute Research Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
inspiratory muscle strength training, coronary artery disease, positron emission tomography, myocardial blood flow

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
High-intensity IMST
Arm Type
Active Comparator
Arm Description
Participants who will be trained with high-intensity IMST
Arm Title
Low-intensity IMST
Arm Type
Sham Comparator
Arm Description
Participants who will be trained with low-intensity IMST
Intervention Type
Device
Intervention Name(s)
High-intensity IMST
Intervention Description
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.
Intervention Type
Device
Intervention Name(s)
Low-intensity IMST
Intervention Description
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.
Primary Outcome Measure Information:
Title
Global myocardial flow reserve
Description
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
Title
Global stress myocardial blood flow
Description
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
Secondary Outcome Measure Information:
Title
Global rest myocardial blood flow
Description
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
Title
Maximum myocardial flow reserve
Description
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
Title
Maximum myocardial blood flow at rest and stress
Description
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
Title
Global coronary vascular resistance at stress and rest
Description
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
Title
Maximum coronary vascular resistance at stress and rest
Description
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
Title
Mean segmental (17-segment model) myocardial flow reserve
Description
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
Title
Mean segmental (17-segment model) myocardial blood flow at stress and rest
Description
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
Title
Maximal segmental (17-segment model) myocardial blood flow at stress and rest
Description
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
Title
Summed stress score, summed rest score, and summed difference score
Description
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
Title
% left ventricular ischemia
Description
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
Title
General quality of life
Description
Change in general Quality of life assessed using the EQ5D-5L
Time Frame
Through study completion, an average of 8 weeks
Title
Angina symptom
Description
Change in angina symptom assessed using the Seattle angina Questionnaire
Time Frame
Through study completion, an average of 8 weeks
Title
Adherence of IMST program
Description
The proportion of participants adhering to prescribed IMST sessions
Time Frame
Through study completion, an average of 8 weeks
Title
Respiratory Muscle Strength
Description
Respiratory Muscle Strength assessed by % change in maximal inspiratory pressure
Time Frame
Through study completion, an average of 8 weeks
Title
Resting blood pressure
Description
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

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: ≥18 years of age; Patients referred to PET at the University of Ottawa Heart Institute; able to perform a respiratory exercise testing; and, Patients with clinical stability, including no change in medications for the past one month. Exclusion criteria: unstable angina or established diagnosis of severe valvular heart disease, hypertrophic obstructive cardiomyopathy, chronic obstructive pulmonary disease; unable to follow training/breathing instructions; unable to return for follow-up visit; presence of any major non-cardiac problem that would adversely affect survival during the study in the opinion of the investigator; or, unable to provide informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Benjamin Chow, MD
Phone
613-696-7286
Email
BChow@ottawaheart.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Yoshito Kadoya, MD, PhD
Phone
613-696-7286
Email
YKadoya@ottawaheart.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benjamin Chow, MD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Ottawa Heart Institute
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 1J7
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yoshito Kadoya, MD, PhD
Phone
6136967068
Email
YKadoya@ottawaheart.ca

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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Blood Flow Reserve: Effects After Training With Heavy Inspiratory Exercises

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