High Intensity Exercise for Increasing Fitness in Patients With Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
About this trial
This is an interventional treatment trial for Hypertrophic Cardiomyopathy focused on measuring High intensity exercise, Cardiorespiratory fitness, Stroke volume reserve, Arrhythmia burden
Eligibility Criteria
Inclusion Criteria:
- Male and female patients aged 18 - 80 years old
- Diagnosed HCM defined by the presence of unexplained left-ventricular hypertrophy with end-diastolic wall thickness ≥ 15 mm on 2D echocardiography or wall thickness between 13 and 15 mm along with at least one other piece of evidence of hypertrophic cardiomyopathy, such as systolic anterior motion of the mitral valve leaflets, family history of hypertrophic cardiomyopathy, or positive genetic test result.
Exclusion Criteria:
- A history of exercise-induced syncope or arrhythmias (ventricular tachycardia; sustained or non-sustained)
- Left ventricular outflow obstruction (≥ 50 mm Hg at rest)
- Less than 3 months post septal reduction therapy (surgery or catheter based intervention)
- Pregnancy
- Worsening clinical status or advanced heart failure (New York Heart Association class IV symptoms)
- A hypotensive responsive to exercise (an increase in exercise systolic BP throughout the exercise test of < 20mmHg compared with resting values, or an initial increase in systolic BP > 20mmHg with a subsequent fall by peak exercise of > 20mmHg, or a continuous decrease in systolic BP throughout the test of > 20mmHg, compared with baseline BP)
- Left ventricular systolic dysfunction (left ventricular ejection fraction < 55 % by echocardiography)
- Coronary artery disease as evidenced by prior myocardial infarction or angina
- Cerebrovascular disease as evidenced by prior transient ischemic attack or stroke
- A chronic orthopaedic injury which limits the ability to exercise
- Subjects unable to speak English will not be recruited because of the complex experimental studies and the need for precise communication between the volunteers and the research staff to ensure safety.
Sites / Locations
- The Institute for Exercise and Environmental Medicine
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
High intensity exercise
Moderate intensity exercise
A training program will be developed individually for each subject with the goal of increasing duration and intensity consistent with exercise training principles. Workouts will vary with respect to mode (walk, cycle) and duration (30 - 60 minutes). Each subject will be assigned an exercise physiologist and a heart rate monitor so that each session can be tracked and recorded. The first few exercise training sessions will supervised at our hospital based fitness centre until the subject is confident to complete the training independently. All HIIT sessions will be supervised over the intervention.