Informatie:
Fout:
ID
28087
Beschrijving
The Effect on Depressive Symptoms in ECF Residents With COPD; ODM derived from: https://clinicaltrials.gov/show/NCT00974246
Link
https://clinicaltrials.gov/show/NCT00974246
Trefwoorden
Versies (1)
- 17-12-17 17-12-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
17 december 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Chronic Obstructive Pulmonary Disease NCT00974246
Eligibility Chronic Obstructive Pulmonary Disease NCT00974246
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Obstructive Pulmonary Disease NCT00974246
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Adult | Nursing home resident | Age
Item
adult men and women nursing home residents up to age 95
boolean
C0001675 (UMLS CUI [1])
C0682287 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
C0682287 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
COPD | FEV1/FVC | Anticholinergic Agents
Item
stated diagnosis of copd or fev1/fvc <0.7 or being treated with an anticholinergic
boolean
C0024117 (UMLS CUI [1])
C3815113 (UMLS CUI [2])
C0242896 (UMLS CUI [3])
C3815113 (UMLS CUI [2])
C0242896 (UMLS CUI [3])
Depressive Symptoms MDS
Item
presence of depressive symptoms as measured on mds 3.0 section d sum
boolean
C0086132 (UMLS CUI [1,1])
C1879299 (UMLS CUI [1,2])
C1879299 (UMLS CUI [1,2])
Free of Condition Likely Fatal
Item
free from conditions likely to be fatal within six months
boolean
C0332296 (UMLS CUI [1,1])
C0348080 (UMLS CUI [1,2])
C0750492 (UMLS CUI [1,3])
C1302234 (UMLS CUI [1,4])
C0348080 (UMLS CUI [1,2])
C0750492 (UMLS CUI [1,3])
C1302234 (UMLS CUI [1,4])
Able to read English Language | Comprehension English Language
Item
able to read or understand english
boolean
C0586740 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0233733 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0376245 (UMLS CUI [1,2])
C0233733 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
Informed Consent | Informed Consent Guardian
Item
able and willing to provide informed consent or has a guardian/lar who can provide informed consent
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C1274041 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,1])
C1274041 (UMLS CUI [2,2])
Pregnancy
Item
currently pregnant
boolean
C0032961 (UMLS CUI [1])
Lacking Able to read English Language | Lacking Comprehension English Language
Item
unable to read and understand english
boolean
C0332268 (UMLS CUI [1,1])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0233733 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0233733 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])
Free of Condition Likely Fatal
Item
free from conditions likely to be fatal within six months
boolean
C0332296 (UMLS CUI [1,1])
C0348080 (UMLS CUI [1,2])
C0750492 (UMLS CUI [1,3])
C1302234 (UMLS CUI [1,4])
C0348080 (UMLS CUI [1,2])
C0750492 (UMLS CUI [1,3])
C1302234 (UMLS CUI [1,4])
Enrollment Hospice patient
Item
enrolled in hospice
boolean
C1516879 (UMLS CUI [1,1])
C0745035 (UMLS CUI [1,2])
C0745035 (UMLS CUI [1,2])
Antidepressive Agents
Item
new treatment with antidepressant within the last 90 days.
boolean
C0003289 (UMLS CUI [1])
Advair Diskus
Item
current or recent use (within the last 90 days) of advair diskus
boolean
C0939246 (UMLS CUI [1])
Informed Consent Unwilling | Informed Consent Unable
Item
unwilling or unable to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Discharge Expected
Item
expected to be discharged within 3 months
boolean
C0030685 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
C1517001 (UMLS CUI [1,2])