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High Intensity Exercise for Increasing Fitness in Patients With Hypertrophic Cardiomyopathy

Primary Purpose

Hypertrophic Cardiomyopathy

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
High intensity exercise
Moderate intensity exercise
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Active Comparator

Arm Label

High intensity exercise

Moderate intensity exercise

Arm Description

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.

Outcomes

Primary Outcome Measures

Cardiorespiratory fitness
Change in maximal oxygen uptake (V̇O2max)

Secondary Outcome Measures

Functional diastolic reserve
Change in stroke volume reserve
Safety - Number of adverse events
Adverse events during the study will be recorded
Safety - Number of arrhythmic events
Number of arrhythmic events will be assessed by an implantable loop recorder

Full Information

First Posted
September 19, 2017
Last Updated
February 27, 2023
Sponsor
University of Texas Southwestern Medical Center
Collaborators
Biotronik SE & Co. KG, American College of Sports Medicine, American Heart Association
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1. Study Identification

Unique Protocol Identification Number
NCT03335332
Brief Title
High Intensity Exercise for Increasing Fitness in Patients With Hypertrophic Cardiomyopathy
Official Title
Efficacy of High Intensity Exercise (HIE) for Increasing Cardiorespiratory Fitness in Patients With Hypertrophic Cardiomyopathy (HCM)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
January 31, 2018 (Actual)
Primary Completion Date
July 26, 2022 (Actual)
Study Completion Date
December 20, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center
Collaborators
Biotronik SE & Co. KG, American College of Sports Medicine, American Heart Association

4. Oversight

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

5. Study Description

Brief Summary
Although current clinical guidelines stipulate that patients with hypertrophic cardiomyopathy should not partake in high intensity exercise (HIE) or competitive sport due to safety concerns, there is no clear evidence to support this notion. In fact, two exercise training interventions in this population indicates that regular moderate to vigorous intensity exercise is efficacious for improving exercise capacity and cardiorespiratory fitness, and does not increase arrhythmia burden or adverse events. Moreover, moderate intensity exercise and HIE training significantly increases cardiorespiratory fitness in patients with cardiac disease. Such improvements are associated with substantial reductions in cardiovascular mortality and might outweigh the risk of adverse events in patients with hypertrophic cardiomyopathy (HCM). Having a genetic cardiomyopathy does not grant immunity against lifestyle related cardiometabolic diseases and inactivity is rife in HCM patients likely due to misinformation/education. It is therefore paramount to further explore the benefits of regular moderate intensity exercise and HIE in patients with HCM for proper therapeutic management of the condition.
Detailed Description
Regular exercise reduces the risk of all-cause and cardiovascular mortality in the general population. Specifically, higher cardiorespiratory fitness is associated with a 10 - 20 % reduction in mortality risk for every 1 MET (metabolic equivalent tasks) improvement in fitness. A high degree of fitness is also protective against the development of heart failure and exercise training has become the standard of care for most patients with cardiovascular disease to improve functional capacity, and reduce morbidity and mortality. However, hypertrophic cardiomyopathy, the most common inherited cardiovascular disease, may be an exception. For more than 30 years, hypertrophic cardiomyopathy (HCM) has been identified as the most common cause of death in young athletes, and patients with HCM are excluded from participation in competitive sports. The fear of provocation of sudden cardiac death has often been extended to non-competitive athletic activities in such patients, though there is a distinct lack of evidence about the safety of exercise in this population. A recent multicenter clinical trial provided evidence that moderate intensity exercise (MIE) may be safe in this population, though the increase in fitness with this training paradigm was modest. Alternatively, an extensive series of reviews published over the last five years advocate for high intensity interval training (HIIT) as an efficacious stimulus for increasing cardiorespiratory fitness in clinical adult populations, including those with heart failure. While a pilot investigation and preliminary findings suggest that moderate to vigorous intensity exercise may be safe and efficacious in patients with HCM, and even protective in animal models, there is no Level A or B evidence comparing the efficacy or safety of MIE and high intensity exercise (HIE) training in this patient population to guide exercise prescription. Therefore, the primary purpose of this exercise trial is to compare the efficacy and safety of supervised MIE and HIE training in adults with HCM. Specific aims and hypotheses of the project are as follows: Aim 1: Compare the efficacy of a high intensity and moderate intensity exercise intervention to improve cardiorespiratory fitness and functional diastolic reserve in patients with HCM. Primary hypothesis: HIE will result in greater increases in maximal oxygen uptake (V̇O2max) than MIE in patients with HCM. Secondary hypothesis: HIE will improve stroke volume reserve to a greater degree than MIE in patients with HCM. Aim 2: To evaluate the safety of HIE training in patients with HCM. Hypothesis: Regular exercise training of a high or moderate intensity will be safe (no serious adverse events) in this patient population. Specifically, it is hypothesised that HIE will not increase arrhythmia burden in patients with HCM.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertrophic Cardiomyopathy
Keywords
High intensity exercise, Cardiorespiratory fitness, Stroke volume reserve, Arrhythmia burden

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
29 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High intensity exercise
Arm Type
Experimental
Arm Description
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.
Arm Title
Moderate intensity exercise
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
High intensity exercise
Intervention Description
The exercise groups will receive identical exercise prescription for the first two months of the intervention, after which the HIE group will incorporate HIIT in their exercise regimen. The reason for this approach is to include a period of general conditioning and progressively increase intensity prior to submitting volunteers to HIE. This approach considers participant safety as arrhythmias may be uncovered during the first two months of MIE training. It will also improve participant compliance by increasing exercise self-efficacy and confidence prior to commencing HIIT.
Intervention Type
Behavioral
Intervention Name(s)
Moderate intensity exercise
Intervention Description
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 in both exercise groups (MIE and HIE) will supervised at our hospital based fitness centre until the subject is confident to complete the training independently.
Primary Outcome Measure Information:
Title
Cardiorespiratory fitness
Description
Change in maximal oxygen uptake (V̇O2max)
Time Frame
Five months
Secondary Outcome Measure Information:
Title
Functional diastolic reserve
Description
Change in stroke volume reserve
Time Frame
Five months
Title
Safety - Number of adverse events
Description
Adverse events during the study will be recorded
Time Frame
Ten months
Title
Safety - Number of arrhythmic events
Description
Number of arrhythmic events will be assessed by an implantable loop recorder
Time Frame
Ten months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benjamin D Levine, MD
Organizational Affiliation
University of Texas Southwestern Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Institute for Exercise and Environmental Medicine
City
Dallas
State/Province
Texas
ZIP/Postal Code
75231
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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High Intensity Exercise for Increasing Fitness in Patients With Hypertrophic Cardiomyopathy

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