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Cardiac Autonomic Regulation Enhancement Through Exercise Trial (CARE-E)

Primary Purpose

Cardiovascular Disease, Arrhythmias

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Exercise
Heart Healthy Education
Sponsored by
The Miriam Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiovascular Disease, Arrhythmias focused on measuring Parasympathetic activity, Exercise, Education, Arrhythmias, Defibrillators, Implantable

Eligibility Criteria

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

Inclusion Criteria:

  • adult ICD patients (≥ 18 years of age)
  • received an ICD for secondary prevention, cardiac diagnosis of: ventricular fibrillation, OR ventricular tachycardia, OR cardiac arrest, OR syncope with ventricular tachycardia inducible by programmed stimulation (EPS), AND
  • either diagnosed coronary artery disease AND/OR prior myocardial infarction, or non-ischemic dilated cardiomyopathy
  • meet functional NYHA Class I or II heart failure or angina symptoms
  • ICD patients need to be sedentary, defined as not engaging in structured exercise more than once weekly, or an accumulation of less than 60 minutes of moderate intensity aerobic activity over the course of the week, for the past 3 months.
  • deemed medically stable by their cardiologist and have received approval by their cardiologist to engage in an exercise program
  • Stable (unchanged) cardiac and psychopharmacologic medications in the 3 months prior to study enrollment
  • Able to read and write English
  • able to commit to the 3-month exercise/heart healthy program attending 3 times per week (36 sessions)
  • able to commit to the 3 assessments (pre, post-treatment, 3-month follow-up; 6-month duration)

Exclusion Criteria:

  • Patients who meet functional NYHA Class III or IV heart failure or angina symptoms
  • sinus node dysfunction that requires atrial pacing
  • atrial fibrillation
  • bi-ventricular ICD
  • are pacemaker-dependent
  • diagnosis of Brugada's Syndrome
  • diagnosis of arrhythmogenic right ventricular dysplasia
  • complex congenital heart disease
  • orthopedic restrictions, limitations, or disabilities that would jeopardize the patient's safety during exercise or form completing the treadmill stress test
  • Neurocognitive or cognitive impairments that will result in nonadherence (based on clinical evaluation)
  • Unstable angina
  • resting systolic blood pressure >180mmHg or resting diastolic blood pressure >110mm Hg will be evaluated on a case-by-case basis
  • orthostatic blood pressure drop of >20mm Hg with symptoms
  • critical aortic stenosis (peak systolic pressure gradient >50mm Hg with aortic valve orifice area <0.75cm2 in average size adult)
  • acute systemic illness or fever
  • uncontrolled atrial or ventricular arrhythmias
  • uncontrolled sinus tachycardia (>120 beats/min)
  • uncompensated CHF
  • 3rd degree AV block (without pacemaker)
  • active pericarditis or myocarditis
  • recent embolism; thrombophlebitis
  • resting ST segment displacement (>2mm)
  • uncontrolled diabetes (resting blood glucose >400mg/dl)
  • metabolic problems, such as acute, hypo or hyperkalemia, hypovolemia
  • recent strongly positive exercise test as achieved by: significant decrease in systolic blood pressure with increasing workload, OR early onset, horizontal or downsloping ST segment depression (4mm), OR prolonged electrocardiogram (ECG) changes during recovery
  • hypertrophic obstructive cardiomyopathy
  • severe pulmonary hypertension
  • patients who do not pass the exercise stress test

Sites / Locations

  • The Miriam Hospital Centers for Behavioral and Preventive Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Exercise

Heart Healthy Education

Arm Description

moderate-intensity, low-impact, supervised, aerobic exercise

Educational topics on heart health (e.g., nutrition, smoking, sleep)

Outcomes

Primary Outcome Measures

parasympathetic activity and regulation

Secondary Outcome Measures

arrhythmia frequency
ICD therapy frequency
exercise tolerance
psychological well-being
quality of life

Full Information

First Posted
February 13, 2009
Last Updated
January 7, 2014
Sponsor
The Miriam Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00845091
Brief Title
Cardiac Autonomic Regulation Enhancement Through Exercise Trial
Acronym
CARE-E
Official Title
Cardiac Autonomic Regulation Enhancement Through Exercise Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
February 2009 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Miriam Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The current research study proposes to examine participants with implantable cardioverter defibrillators (ICD) who are randomly assigned to either an exercise training program intervention or a heart healthy education program intervention. We will look at changes in the functioning of the autonomic nervous system over time and between intervention groups. We are also going to be looking at changes in frequencies of the ICD participants' heart arrhythmias and ICD therapies (e.g., pacing, shock).; as well as, changes in exercise tolerance, psychological well-being, and quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Disease, Arrhythmias
Keywords
Parasympathetic activity, Exercise, Education, Arrhythmias, Defibrillators, Implantable

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise
Arm Type
Experimental
Arm Description
moderate-intensity, low-impact, supervised, aerobic exercise
Arm Title
Heart Healthy Education
Arm Type
Active Comparator
Arm Description
Educational topics on heart health (e.g., nutrition, smoking, sleep)
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
moderate-intensity, low-impact, supervised, aerobic exercise
Intervention Type
Behavioral
Intervention Name(s)
Heart Healthy Education
Intervention Description
Educational topics related to heart health (e.g., nutrition, smoking, sleep)
Primary Outcome Measure Information:
Title
parasympathetic activity and regulation
Time Frame
3 months, 6 months
Secondary Outcome Measure Information:
Title
arrhythmia frequency
Time Frame
3 months, 6 months
Title
ICD therapy frequency
Time Frame
3 months, 6 months
Title
exercise tolerance
Time Frame
3 months, 6 months
Title
psychological well-being
Time Frame
3 months, 6 months
Title
quality of life
Time Frame
3 months, 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult ICD patients (≥ 18 years of age) received an ICD for secondary prevention, cardiac diagnosis of: ventricular fibrillation, OR ventricular tachycardia, OR cardiac arrest, OR syncope with ventricular tachycardia inducible by programmed stimulation (EPS), AND either diagnosed coronary artery disease AND/OR prior myocardial infarction, or non-ischemic dilated cardiomyopathy meet functional NYHA Class I or II heart failure or angina symptoms ICD patients need to be sedentary, defined as not engaging in structured exercise more than once weekly, or an accumulation of less than 60 minutes of moderate intensity aerobic activity over the course of the week, for the past 3 months. deemed medically stable by their cardiologist and have received approval by their cardiologist to engage in an exercise program Stable (unchanged) cardiac and psychopharmacologic medications in the 3 months prior to study enrollment Able to read and write English able to commit to the 3-month exercise/heart healthy program attending 3 times per week (36 sessions) able to commit to the 3 assessments (pre, post-treatment, 3-month follow-up; 6-month duration) Exclusion Criteria: Patients who meet functional NYHA Class III or IV heart failure or angina symptoms sinus node dysfunction that requires atrial pacing atrial fibrillation bi-ventricular ICD are pacemaker-dependent diagnosis of Brugada's Syndrome diagnosis of arrhythmogenic right ventricular dysplasia complex congenital heart disease orthopedic restrictions, limitations, or disabilities that would jeopardize the patient's safety during exercise or form completing the treadmill stress test Neurocognitive or cognitive impairments that will result in nonadherence (based on clinical evaluation) Unstable angina resting systolic blood pressure >180mmHg or resting diastolic blood pressure >110mm Hg will be evaluated on a case-by-case basis orthostatic blood pressure drop of >20mm Hg with symptoms critical aortic stenosis (peak systolic pressure gradient >50mm Hg with aortic valve orifice area <0.75cm2 in average size adult) acute systemic illness or fever uncontrolled atrial or ventricular arrhythmias uncontrolled sinus tachycardia (>120 beats/min) uncompensated CHF 3rd degree AV block (without pacemaker) active pericarditis or myocarditis recent embolism; thrombophlebitis resting ST segment displacement (>2mm) uncontrolled diabetes (resting blood glucose >400mg/dl) metabolic problems, such as acute, hypo or hyperkalemia, hypovolemia recent strongly positive exercise test as achieved by: significant decrease in systolic blood pressure with increasing workload, OR early onset, horizontal or downsloping ST segment depression (4mm), OR prolonged electrocardiogram (ECG) changes during recovery hypertrophic obstructive cardiomyopathy severe pulmonary hypertension patients who do not pass the exercise stress test
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eva R Serber, Ph.D.
Organizational Affiliation
The Miriam Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Miriam Hospital Centers for Behavioral and Preventive Medicine
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States

12. IPD Sharing Statement

Citations:
Citation
Palmer K, Tilkemeier PL, Buxton AE, Niaura R, Marcus B, Todaro J, Serber ER. Ratings of perceived exertion and physiological responses during exercise testing among ICD patients. Poster presented at the 32nd Annual Meeting of the Society for Behavioral Medicine, New Orleans, LA.; Abstract B-1621, Rapid Communications, April 2012.
Results Reference
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Cardiac Autonomic Regulation Enhancement Through Exercise Trial

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