Age
Item
1. subjects 30-65 years old.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
2. subjects able to give informed consent.
boolean
C0021430 (UMLS CUI [1])
Permission Data Collection Electronic Health Records
Item
3. subjects who will give permission for collection of clinical and demographic data from the electronic medical records.
boolean
C0521104 (UMLS CUI [1,1])
C0010995 (UMLS CUI [1,2])
C2362543 (UMLS CUI [1,3])
Heart failure Symptomatic New York Heart Association Classification | Heart failure Ischemic Symptomatic | Heart failure Stable Disease length
Item
4. subjects with symptomatic ischemic or non-ischemic heart failure in a stable condition with new york heart association class ii-iii for at least the last 3 months before study enrollment.
boolean
C0018801 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
C0018801 (UMLS CUI [2,1])
C0475224 (UMLS CUI [2,2])
C0231220 (UMLS CUI [2,3])
C0018801 (UMLS CUI [3,1])
C0205360 (UMLS CUI [3,2])
C0872146 (UMLS CUI [3,3])
Left ventricular ejection fraction
Item
left ventricular ejection fraction (lvef) < 40%.
boolean
C0428772 (UMLS CUI [1])
VO2 Peak
Item
peak volume of oxygen utilization (peak vo2) of < 25 ml/kg/min.
boolean
C1305742 (UMLS CUI [1,1])
C0444505 (UMLS CUI [1,2])
Statin Dose Stable | Initiation Statin therapy possible
Item
5. patient on a stable dose of statin or who can be initiated on statin therapy.
boolean
C0360714 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C1704686 (UMLS CUI [2,1])
C1278454 (UMLS CUI [2,2])
C0332149 (UMLS CUI [2,3])
Ischemic cardiomyopathy Stress Test Negative | Disease Stable Cardiac Catheterization
Item
6. subjects with ischemic cardiomyopathy must have had either a negative stress test within the last 6 months or a cardiac catheterization within the last year confirming stable disease.
boolean
C0349782 (UMLS CUI [1,1])
C3494508 (UMLS CUI [1,2])
C1513916 (UMLS CUI [1,3])
C0012634 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0018795 (UMLS CUI [2,3])
Myocardial Infarction | Angina, Unstable
Item
1. subjects with myocardial infarction or unstable angina within the last six months.
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
Aortic stenosis symptomatic | Aortic stenosis, severe
Item
2. subjects with symptomatic or severe aortic stenosis.
boolean
C0741183 (UMLS CUI [1])
C3806272 (UMLS CUI [2])
Hypertension, severe | Systolic Pressure | Hypotension, severe
Item
3. subjects with severe htn (sbp > 180) or hypotension (sbp < 100).
boolean
C4013784 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C2678378 (UMLS CUI [3])
Pregnancy
Item
4. subjects who are pregnant.
boolean
C0032961 (UMLS CUI [1])
Bone Marrow Suppression
Item
5. subjects who have bone marrow suppression.
boolean
C0280962 (UMLS CUI [1])
Peripheral Arterial Disease Limiting Exercise
Item
6. subjects with exercise limiting peripheral arterial disease.
boolean
C1704436 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
Tachycardia, Ventricular | Implantable defibrillator Absent
Item
7. subjects with history of ventricular tachycardia without an implantable defibrillator
boolean
C0042514 (UMLS CUI [1])
C0162589 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
DIABETES MELLITUS DECOMPENSATED | Hemoglobin A1c measurement
Item
8. subjects with decompensated diabetes (hga1c >10).
boolean
C0743120 (UMLS CUI [1])
C0474680 (UMLS CUI [2])
Orthopedic problem
Item
9. subjects with orthopedic limitations.
boolean
C0029354 (UMLS CUI [1])
Medical condition Excludes Walking Exercise
Item
10. subjects with any other clinical condition precluding regular participation in walking exercise regimen.
boolean
C3843040 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0080331 (UMLS CUI [1,3])
C0015259 (UMLS CUI [1,4])
Participates in regular exercise Duration Frequency
Item
11. subjects who already participate in regular physical exercise regimen for greater than 30 minutes a day 5 days per week.
boolean
C1821438 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])