ID

28087

Description

The Effect on Depressive Symptoms in ECF Residents With COPD; ODM derived from: https://clinicaltrials.gov/show/NCT00974246

Link

https://clinicaltrials.gov/show/NCT00974246

Keywords

Versions (1)
  1. 12/17/17 12/17/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

December 17, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Chronic Obstructive Pulmonary Disease NCT00974246

English

Eligibility Chronic Obstructive Pulmonary Disease NCT00974246

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult men and women nursing home residents up to age 95
Description

Adult | Nursing home resident | Age

Data type

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0682287
UMLS CUI [3]
C0001779
stated diagnosis of copd or fev1/fvc <0.7 or being treated with an anticholinergic
Description

COPD | FEV1/FVC | Anticholinergic Agents

Data type

boolean

Alias
UMLS CUI [1]
C0024117
UMLS CUI [2]
C3815113
UMLS CUI [3]
C0242896
presence of depressive symptoms as measured on mds 3.0 section d sum
Description

Depressive Symptoms MDS

Data type

boolean

Alias
UMLS CUI [1,1]
C0086132
UMLS CUI [1,2]
C1879299
free from conditions likely to be fatal within six months
Description

Free of Condition Likely Fatal

Data type

boolean

Alias
UMLS CUI [1,1]
C0332296
UMLS CUI [1,2]
C0348080
UMLS CUI [1,3]
C0750492
UMLS CUI [1,4]
C1302234
able to read or understand english
Description

Able to read English Language | Comprehension English Language

Data type

boolean

Alias
UMLS CUI [1,1]
C0586740
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0233733
UMLS CUI [2,2]
C0376245
able and willing to provide informed consent or has a guardian/lar who can provide informed consent
Description

Informed Consent | Informed Consent Guardian

Data type

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1274041
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
currently pregnant
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
unable to read and understand english
Description

Lacking Able to read English Language | Lacking Comprehension English Language

Data type

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0586740
UMLS CUI [1,3]
C0376245
UMLS CUI [2,1]
C0332268
UMLS CUI [2,2]
C0233733
UMLS CUI [2,3]
C0376245
free from conditions likely to be fatal within six months
Description

Free of Condition Likely Fatal

Data type

boolean

Alias
UMLS CUI [1,1]
C0332296
UMLS CUI [1,2]
C0348080
UMLS CUI [1,3]
C0750492
UMLS CUI [1,4]
C1302234
enrolled in hospice
Description

Enrollment Hospice patient

Data type

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C0745035
new treatment with antidepressant within the last 90 days.
Description

Antidepressive Agents

Data type

boolean

Alias
UMLS CUI [1]
C0003289
current or recent use (within the last 90 days) of advair diskus
Description

Advair Diskus

Data type

boolean

Alias
UMLS CUI [1]
C0939246
unwilling or unable to provide informed consent
Description

Informed Consent Unwilling | Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
expected to be discharged within 3 months
Description

Discharge Expected

Data type

boolean

Alias
UMLS CUI [1,1]
C0030685
UMLS CUI [1,2]
C1517001
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Similar models

Eligibility Chronic Obstructive Pulmonary Disease NCT00974246

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
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])
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])
Enrollment Hospice patient
Item
enrolled in hospice
boolean
C1516879 (UMLS CUI [1,1])
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])
Discharge Expected
Item
expected to be discharged within 3 months
boolean
C0030685 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
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