Rheumatoid Arthritis
Item
males and females with ra
boolean
C0003873 (UMLS CUI [1])
Age
Item
over 18 years of age
boolean
C0001779 (UMLS CUI [1])
Rheumatoid Arthritis Class Functional
Item
acr functional class i and ii
boolean
C0003873 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
C0205245 (UMLS CUI [1,3])
Remicade
Item
taking remicade >4 months
boolean
C0723012 (UMLS CUI [1])
Medical contraindication Exercise
Item
presence of comorbid conditions contraindicated to exercise, including, but not limited to:
boolean
C1301624 (UMLS CUI [1,1])
C0015259 (UMLS CUI [1,2])
Heart Disease
Item
1. heart disease
boolean
C0018799 (UMLS CUI [1])
Severe osteoporosis T score | Severe osteoporosis T score Hip | Severe osteoporosis T score Vertebral column
Item
2. severe osteoporosis: (if >50 years): t score < -3.0 for hip or spine excluded; t score <-2.5 for hip or spine w/o current treatment)
boolean
C1859443 (UMLS CUI [1,1])
C3854607 (UMLS CUI [1,2])
C1859443 (UMLS CUI [2,1])
C3854607 (UMLS CUI [2,2])
C0019552 (UMLS CUI [2,3])
C1859443 (UMLS CUI [3,1])
C3854607 (UMLS CUI [3,2])
C0037949 (UMLS CUI [3,3])
Fracture
Item
3. (all potential subjects) previous non-traumatic fractures
boolean
C0016658 (UMLS CUI [1])
Blood Pressure Uncontrolled
Item
4. uncontrolled bp
boolean
C0005823 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Body mass index
Item
bmi >40
boolean
C1305855 (UMLS CUI [1])
Walking assistive device Using Regular | Weight Lifting Ability Affected
Item
regular use of assistive walking device which would interfere with ability to lift weights
boolean
C3874140 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
C0205272 (UMLS CUI [1,3])
C0043095 (UMLS CUI [2,1])
C0085732 (UMLS CUI [2,2])
C0392760 (UMLS CUI [2,3])
Aerobic Exercise participation
Item
currently or within the last 3 months participating in aerobic exercise > 150 minutes a week
boolean
C0001701 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
Resistance Training Regular participation
Item
currently or within the last 3 months participating in any regular strength training activities
boolean
C0872279 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
Neurologic Deficits Limiting Exercise
Item
presence of neurological impairment that directly limits ability to perform exercise
boolean
C0521654 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
Study Subject Participation Status | Clinical Trial Exercise
Item
participation in concurrent exercise study
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0015259 (UMLS CUI [2,2])
Indication Discontinuation Clinical Trial
Item
any reason for which the investigator deems it would not be in the patient’s best interest to continue in the study
boolean
C0392360 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Relocation of home Planned
Item
plans to move away from site within next 1 year
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])