Informationen:
Fehler:
ID
40775
Beschreibung
Corticospinal Excitability and Rehab in Knee Osteoarthritis; ODM derived from: https://clinicaltrials.gov/show/NCT02036866
Link
https://clinicaltrials.gov/show/NCT02036866
Stichworte
Versionen (1)
- 11.05.20 11.05.20 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
11. Mai 2020
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Knee Osteoarthritis NCT02036866
Eligibility Knee Osteoarthritis NCT02036866
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Knee Osteoarthritis NCT02036866
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Age
Item
age 19-65
boolean
C0001779 (UMLS CUI [1])
Knee Osteoarthritis Grade Radiography | Knee Osteoarthritis Grade Imaging
Item
grade i or ii knee osteoarthritis confirmed by radiographs or other imaging and at least one of the following:
boolean
C0409959 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C0034571 (UMLS CUI [1,3])
C0409959 (UMLS CUI [2,1])
C0441800 (UMLS CUI [2,2])
C0011923 (UMLS CUI [2,3])
C0441800 (UMLS CUI [1,2])
C0034571 (UMLS CUI [1,3])
C0409959 (UMLS CUI [2,1])
C0441800 (UMLS CUI [2,2])
C0011923 (UMLS CUI [2,3])
Age
Item
age > 50 years old
boolean
C0001779 (UMLS CUI [1])
Morning stiffness Duration
Item
morning stiffness < 30 minutes
boolean
C0457086 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
Crepitus
Item
crepitus
boolean
C0277964 (UMLS CUI [1])
Diagnostic criteria Fulfill Osteoarthritis
Item
meet at least 3 of 6 diagnostic criteria for osteoarthritis:
boolean
C0679228 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
C0029408 (UMLS CUI [1,3])
C1550543 (UMLS CUI [1,2])
C0029408 (UMLS CUI [1,3])
Age
Item
age > 50 years old
boolean
C0001779 (UMLS CUI [1])
Morning stiffness Duration
Item
morning stiffness < 30 minutes
boolean
C0457086 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
Crepitus
Item
crepitus
boolean
C0277964 (UMLS CUI [1])
Bone tenderness
Item
bony tenderness
boolean
C0238807 (UMLS CUI [1])
Bony joint enlargement
Item
bony enlargement
boolean
C0221610 (UMLS CUI [1])
Warmth Palpable Lacking
Item
no palpable warmth
boolean
C0392197 (UMLS CUI [1,1])
C0522499 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
C0522499 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Body mass index
Item
bmi > 30
boolean
C1305855 (UMLS CUI [1])
Spinal Injury | Lower extremity Injury
Item
history of traumatic spine or lower extremity injury within the last 6 months
boolean
C0037937 (UMLS CUI [1])
C0023220 (UMLS CUI [2])
C0023220 (UMLS CUI [2])
Adverse reaction Electric stimulation | Burns | Hypersensitivity
Item
previous adverse reaction to electrical stimulation (i.e. burns or hypersensitivity)
boolean
C0559546 (UMLS CUI [1,1])
C0013786 (UMLS CUI [1,2])
C0006434 (UMLS CUI [2])
C0020517 (UMLS CUI [3])
C0013786 (UMLS CUI [1,2])
C0006434 (UMLS CUI [2])
C0020517 (UMLS CUI [3])
Artificial cardiac pacemaker
Item
cardiac pacemaker
boolean
C0030163 (UMLS CUI [1])
Metallic implant Head
Item
metal implants in head
boolean
C3693688 (UMLS CUI [1,1])
C0018670 (UMLS CUI [1,2])
C0018670 (UMLS CUI [1,2])
Pregnancy
Item
current pregnancy
boolean
C0032961 (UMLS CUI [1])
Nervous system disorder
Item
neurological disorders
boolean
C0027765 (UMLS CUI [1])
Seizures
Item
history of seizures
boolean
C0036572 (UMLS CUI [1])
Informed Consent Unable | Comprehension Study Protocol Unable
Item
unable to give consent or understand the procedures of this study
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C1299582 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])