Prevention Using Exercise Rehabilitation to Offset Cardiac Toxicities Induced Via Chemotherapy (HF-PROACTIVE)
Primary Purpose
Doxorubicin Induced Cardiomyopathy, Breast Cancer, Gastric Cancer
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise
Sponsored by
About this trial
This is an interventional prevention trial for Doxorubicin Induced Cardiomyopathy focused on measuring Exercise, Cancer, Cardiotoxicity, Cardiomyopathy, Cardiac Rehabilitation
Eligibility Criteria
Inclusion Criteria:
- Patients with cancer who are undergoing or have completed the chemotherapy drugs doxorubicin and/or trastuzumab.
- Have had a recent echocardiogram with a relative reduction in LV strain of >10%.
- If no recent echocardiogram, have a troponin value >0.04 ng/mL, or an increase of 0.04 ng/mL if baseline troponin is elevated.
- Age >/= 18 years.
- Eastern Cooperative Oncology Group (ECOG) scale 0-2.
- Males and females.
Exclusion Criteria:
- Patients with an Ejection Fraction <50%
- Patients not deemed appropriate by a cardiologist or oncologist
- Patients with an ECOG scale >2
- Inability to perform exercise
- Patients who already report exercising >2days per week for >29 minutes
Sites / Locations
- William Clay Ford Center for Athletic Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Exercise
Usual care
Arm Description
Patients will participate in a 10 week outpatient cardiac rehabilitation program. Exercise will consist of 3 days per week of interval training on a treadmill or bike at an intensity between 50-90% of heart rate reserve. Additionally patients will perform resistance exercises 1-2 days per week and attend 8 nutrition and lifestyle classes.
Control group will not be instructed on exercise, but encouraged to follow standard medical advice.
Outcomes
Primary Outcome Measures
Left ventricular strain
Spectral Doppler measure with General Electric software analysis of global longitudinal strain.
Secondary Outcome Measures
Peak VO2
During a graded treadmill test, breath-by-breath sampling of expired air will be measured using a MGC Diagnostics gas exchange analysis system.
Percent body fat
Body fat will be analyzed using air displacement plethysmography (BodPod/Cosmed)
Isokinetic strength
Peak torque will be measured using the Biodex Isokinetic dynamometer.
Quality of life
Quality of life will be assessed using the Functional Assessment of Cancer Therapy (FACT-G).
Cardiac Troponin
High sensitivity cardiac troponin will be analyzed using a commercial immunoassay.
Full Information
NCT ID
NCT02796365
First Posted
April 29, 2016
Last Updated
December 12, 2018
Sponsor
Henry Ford Health System
Collaborators
Helen L. Kay Charitable Trust
1. Study Identification
Unique Protocol Identification Number
NCT02796365
Brief Title
Prevention Using Exercise Rehabilitation to Offset Cardiac Toxicities Induced Via Chemotherapy
Acronym
HF-PROACTIVE
Official Title
Prevention Using Exercise Rehabilitation to Offset Cardiac Toxicities Induced Via Chemotherapy
Study Type
Interventional
2. Study Status
Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
June 2016 (undefined)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
December 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Henry Ford Health System
Collaborators
Helen L. Kay Charitable Trust
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to identify patients at risk for future heart failure using novel markers of early cardiac damage and determine if exercise training can improve these emerging markers as well as overall fitness and quality of life.
Detailed Description
With more than 14 million cancer survivors in the United States, more patients than ever are living well beyond their initial cancer diagnosis. However despite the tremendous progress, cancer treatments often come with adverse side-effects, perhaps none are more serious or devastating than chemotherapy induced heart failure.
In many patients, the clinical manifestation of heart failure may not appear until a year, or several years, after completion of chemotherapy. While an echocardiogram is part of standardized surveillance for patients on these drugs, current echocardiogram parameters may not be sensitive enough to quickly detect early heart damage which, in some cases, is irreversible.
Unfortunately, even if detected early, there is no uniformity in terms of how to best treat patients with subclinical cardiac dysfunction who are at risk for heart failure. The use of certain blood pressure drugs show promise, especially in patients with hypertension. However, in addition to drug side-effects (e.g. dizziness/lightheadedness), they do not target the underlying mechanism of chemotherapy induced cardiotoxicity.
Exercise, in various forms, has shown promise in animal studies as a potential cardio-protective therapy to counteract drug toxicity. In general, exercise has many pleiotropic effects for patients receiving chemotherapy (e.g. reduces fatigue, improves endurance, reduces frailty, and enhances quality of life). Relative to DOX toxicity, research involving animals has also shown that exercise protects against deleterious heart dysfunction while showing an enhancement of potential mechanisms involved in chemotherapy induced heart failure (i.e. anti-oxidant and anti-apoptosis pathways).
Patients with cancer who receive either doxorubicin (DOX) or trastuzumab will be screened by one of two methods: 1) a strain echo or 2) a high sensitivity troponin. If either test is positive, patients will meet with a board-certified cardiologist who will determine if the patient may participate in the exercise trial. Under the supervision of a trained clinical exercise physiologist patients will undergo baseline testing, which includes: a quality of life assessment via questionaires, a body composition test, cardiopulmonary stress test and a muscle strength test. These assessment will be performed at baseline and at 12 weeks. Also performed at 12 weeks will be a repeat strain echo and high sensitivity troponin.
Following baseline testing patients will be randomized into exercise training versus standard care. The exercise training will include 12 weeks of cardiac rehabilitation which can be offered in Detroit, Livonia, or West Bloomfield. Exercise will consist of 3 days per week of an interval training aerobic exercise on a treadmill and/or bike for 30-60 minutes and 1-2 days per week of an individualized resistance training program.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Doxorubicin Induced Cardiomyopathy, Breast Cancer, Gastric Cancer, Leukemia
Keywords
Exercise, Cancer, Cardiotoxicity, Cardiomyopathy, Cardiac Rehabilitation
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
29 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Exercise
Arm Type
Experimental
Arm Description
Patients will participate in a 10 week outpatient cardiac rehabilitation program. Exercise will consist of 3 days per week of interval training on a treadmill or bike at an intensity between 50-90% of heart rate reserve. Additionally patients will perform resistance exercises 1-2 days per week and attend 8 nutrition and lifestyle classes.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Control group will not be instructed on exercise, but encouraged to follow standard medical advice.
Intervention Type
Other
Intervention Name(s)
Exercise
Intervention Description
Intervention will include 10 weeks of a standard cardiac rehabilitation program consisting of thrice a week aerobic exercise and 1-2 days per week resistance exercises.
Primary Outcome Measure Information:
Title
Left ventricular strain
Description
Spectral Doppler measure with General Electric software analysis of global longitudinal strain.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Peak VO2
Description
During a graded treadmill test, breath-by-breath sampling of expired air will be measured using a MGC Diagnostics gas exchange analysis system.
Time Frame
12 weeks
Title
Percent body fat
Description
Body fat will be analyzed using air displacement plethysmography (BodPod/Cosmed)
Time Frame
12 weeks
Title
Isokinetic strength
Description
Peak torque will be measured using the Biodex Isokinetic dynamometer.
Time Frame
12 weeks
Title
Quality of life
Description
Quality of life will be assessed using the Functional Assessment of Cancer Therapy (FACT-G).
Time Frame
12 weeks
Title
Cardiac Troponin
Description
High sensitivity cardiac troponin will be analyzed using a commercial immunoassay.
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with cancer who are undergoing or have completed the chemotherapy drugs doxorubicin and/or trastuzumab.
Have had a recent echocardiogram with a relative reduction in LV strain of >10%.
If no recent echocardiogram, have a troponin value >0.04 ng/mL, or an increase of 0.04 ng/mL if baseline troponin is elevated.
Age >/= 18 years.
Eastern Cooperative Oncology Group (ECOG) scale 0-2.
Males and females.
Exclusion Criteria:
Patients with an Ejection Fraction <50%
Patients not deemed appropriate by a cardiologist or oncologist
Patients with an ECOG scale >2
Inability to perform exercise
Patients who already report exercising >2days per week for >29 minutes
Facility Information:
Facility Name
William Clay Ford Center for Athletic Medicine
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Prevention Using Exercise Rehabilitation to Offset Cardiac Toxicities Induced Via Chemotherapy
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