Informatie:
Fout:
ID
39976
Beschrijving
Measuring Adherence to Control Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01257347
Link
https://clinicaltrials.gov/show/NCT01257347
Trefwoorden
Versies (1)
- 07-03-20 07-03-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
7 maart 2020
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT01257347
Eligibility Hypertension NCT01257347
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT01257347
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Hypertensive disease
Item
clinical diagnosis of hypertension
boolean
C0020538 (UMLS CUI [1])
Antihypertensive Agents prescribed Quantity
Item
prescribed at least one blood pressure medication
boolean
C0003364 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0278329 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Blood Pressure Uncontrolled | Systolic Pressure | Diastolic blood pressure | Diabetes Mellitus Absent | Chronic Kidney Disease Absent | Glomerular Filtration Rate
Item
uncontrolled blood pressure on at least 2 clinic visits (sbp ≥140 or dbp≥90 if no diabetes mellitus (dm) or chronic kidney disease (ckd; glomerular filtration rate <60ml/min); sbp ≥130 or dbp ≥80 if dm or ckd)
boolean
C0005823 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0011849 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C1561643 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
C0017654 (UMLS CUI [6])
C0205318 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0011849 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C1561643 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
C0017654 (UMLS CUI [6])
Lacking Able to speak English Language | Lacking Able to speak Spanish Language
Item
non-english, non-spanish speaking
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0564215 (UMLS CUI [2,2])
C0037750 (UMLS CUI [2,3])
C0564215 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0564215 (UMLS CUI [2,2])
C0037750 (UMLS CUI [2,3])
Institutional resident
Item
live in institutional setting
boolean
C0682286 (UMLS CUI [1])
Severe visual impairment
Item
severe visual impairment
boolean
C1301509 (UMLS CUI [1])
Terminal illness | Exception Cardiovascular Disease | Prognosis bad
Item
terminal non-cardiovascular illness (<6 month prognosis)
boolean
C0679247 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007222 (UMLS CUI [2,2])
C0278252 (UMLS CUI [3])
C1705847 (UMLS CUI [2,1])
C0007222 (UMLS CUI [2,2])
C0278252 (UMLS CUI [3])
Study Subject Participation Status | Clinical Trial Cardiovascular
Item
simultaneously enrolled in another cardiovascular trial
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C3887460 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,1])
C3887460 (UMLS CUI [2,2])
Adherence Follow-up Unable
Item
unable to return for follow-up
boolean
C1510802 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C3274571 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Access to telephone Lacking
Item
no access to a telephone
boolean
C1822200 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
Age
Item
age>80
boolean
C0001779 (UMLS CUI [1])