Parkinson Disease
Item
neurologist-diagnosed idiopathic pd based on the uk pd brain bank criteria
boolean
C0030567 (UMLS CUI [1])
Age
Item
aged 45-85
boolean
C0001779 (UMLS CUI [1])
Parkinson Disease Mild Hoehn and Yahr Stage | Parkinson Disease Moderate Hoehn and Yahr Stage
Item
hoehn and yahr stages 1-3 (mild to moderate pd)
boolean
C0030567 (UMLS CUI [1,1])
C2945599 (UMLS CUI [1,2])
C3639483 (UMLS CUI [1,3])
C0030567 (UMLS CUI [2,1])
C0205081 (UMLS CUI [2,2])
C3639483 (UMLS CUI [2,3])
Change of medication Absent | Change Operative Surgical Procedures Absent
Item
participants do not anticipate a change in medication or surgical procedures in the next 8 months of the trial (2 months for the trial and 6 for the follow-up)
boolean
C0580105 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392747 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Study Subject Participation Status Approved
Item
clearance from primary care physician to participate in the trial
boolean
C2348568 (UMLS CUI [1,1])
C0205540 (UMLS CUI [1,2])
Antiparkinson Agents Stable | Deep Brain Stimulation Stable
Item
must be stable on pd medication and dbs for 3 months prior to trial
boolean
C0003405 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0394162 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
Cardiovascular Disease Poorly controlled | Cardiovascular Disease Unstable | Exercise participation Excluded
Item
poorly controlled or unstable cardiovascular disease that precludes participation in exercise
boolean
C0007222 (UMLS CUI [1,1])
C3853134 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
C0015259 (UMLS CUI [3,1])
C0679823 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])
Moderate dementia Montreal cognitive assessment | Severe dementia Montreal cognitive assessment
Item
moderate-to-severe dementia using the montreal cognitive assessment (moca). we will exclude participants with a moca cut off score of <26/30. this cut off value has excellent sensitivity (90%) and specificity (75%).
boolean
C3494871 (UMLS CUI [1,1])
C3496286 (UMLS CUI [1,2])
C3494652 (UMLS CUI [2,1])
C3496286 (UMLS CUI [2,2])
Lacking Able to stand Duration | Lacking Able to walk Duration
Item
inability to stand or walk for more than 10 minutes
boolean
C0332268 (UMLS CUI [1,1])
C0560884 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C2712089 (UMLS CUI [2,2])
C0449238 (UMLS CUI [2,3])
Disease Limiting Exercise | Osteoarthritis | Cerebrovascular accident | Respiratory problem | Traumatic Brain Injury | Neuromuscular Diseases | Pain
Item
other significant disorders that would limit endurance exercise participation (i.e., osteoarthritis, stroke, respiratory problems, traumatic brain injury, neuromuscular disease, pain)
boolean
C0012634 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
C0029408 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C1659989 (UMLS CUI [4])
C0876926 (UMLS CUI [5])
C0027868 (UMLS CUI [6])
C0030193 (UMLS CUI [7])
Regular exercise Frequency | Vigorous exercise intensity Maximum heart rate
Item
already participating in a regular, vigorous exercise program (3x/week or more of >60% estimated maximum heart rate)
boolean
C0582191 (UMLS CUI [1,1])
C0439603 (UMLS CUI [1,2])
C3841230 (UMLS CUI [2,1])
C0744679 (UMLS CUI [2,2])
Medication Interferes with Heart rate response Exercise
Item
participants will be excluded from the trial if they are taking any medications that interfere with heart rate response to exercise
boolean
C0013227 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C1997754 (UMLS CUI [1,3])
C0015259 (UMLS CUI [1,4])