ID

17686

Description

Hypertension Telemanagement in African Americans; ODM derived from: https://clinicaltrials.gov/show/NCT00224861

Link

https://clinicaltrials.gov/show/NCT00224861

Keywords

Versions (1)
  1. 9/28/16 9/28/16 -
Uploaded on

September 28, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Hypertension NCT00224861

English

Eligibility Hypertension NCT00224861

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient must have a primary care provider at one of the clinics participating in the study
Description

Primary care provider Has

Data type

boolean

Alias
UMLS CUI [1,1]
C2735026
UMLS CUI [1,2]
C3539897
physician diagnosis of hypertension
Description

Hypertensive disease

Data type

boolean

Alias
UMLS CUI [1]
C0020538
21 years of age or older at the time of randomization
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
african american by self-report
Description

African American

Data type

boolean

Alias
UMLS CUI [1]
C0085756
taking at least one medication prescribed for hypertension
Description

Prescribed medications Quantity Hypertensive disease

Data type

boolean

Alias
UMLS CUI [1,1]
C3166216
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0020538
poorly controlled blood pressure
Description

Blood Pressure Poorly controlled

Data type

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C3853134
understand spoken english
Description

English Language comprehension

Data type

boolean

Alias
UMLS CUI [1,1]
C0376245
UMLS CUI [1,2]
C0233733
have a home telephone
Description

Home Telephone Has

Data type

boolean

Alias
UMLS CUI [1,1]
C0442519
UMLS CUI [1,2]
C0039457
UMLS CUI [1,3]
C3539897
no other member of the household enrolled in the study
Description

Clinical Trial Enrollment Household member

Data type

boolean

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1516879
UMLS CUI [1,3]
C0020052
UMLS CUI [1,4]
C0680022
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
an identified secondary cause of hypertension
Description

Hypertensive disease Cause Secondary

Data type

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0015127
UMLS CUI [1,3]
C0175668
symptomatic myocardial infarction or stroke within the past 6 months
Description

Myocardial Infarction Symptomatic | Cerebrovascular accident

Data type

boolean

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C0231220
UMLS CUI [2]
C0038454
congestive heart failure (nyha class iii or greater)
Description

Congestive heart failure | New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C1275491
significant renal impairment
Description

Renal Insufficiency Significant

Data type

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C0750502
diseases likely to lead to noncardiovascular death over the course of the study
Description

Disease Resulting in Cessation of life

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0332294
UMLS CUI [1,3]
C0011065
evidence that the patient may move from the study area before the completion of the study
Description

Relocation of home Evidence

Data type

boolean

Alias
UMLS CUI [1,1]
C2699029
UMLS CUI [1,2]
C3887511
presence of any health condition that would preclude participation (e.g., psychiatric diagnosis or physical disability)
Description

medical condition Excludes participation | Diagnosis, Psychiatric | Physical disability

Data type

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0679823
UMLS CUI [2]
C0376338
UMLS CUI [3]
C0520817
active drug use
Description

Drug usage

Data type

boolean

Alias
UMLS CUI [1]
C0242510
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Similar models

Eligibility Hypertension NCT00224861

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Primary care provider Has
Item
patient must have a primary care provider at one of the clinics participating in the study
boolean
C2735026 (UMLS CUI [1,1])
C3539897 (UMLS CUI [1,2])
Hypertensive disease
Item
physician diagnosis of hypertension
boolean
C0020538 (UMLS CUI [1])
Age
Item
21 years of age or older at the time of randomization
boolean
C0001779 (UMLS CUI [1])
African American
Item
african american by self-report
boolean
C0085756 (UMLS CUI [1])
Prescribed medications Quantity Hypertensive disease
Item
taking at least one medication prescribed for hypertension
boolean
C3166216 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0020538 (UMLS CUI [1,3])
Blood Pressure Poorly controlled
Item
poorly controlled blood pressure
boolean
C0005823 (UMLS CUI [1,1])
C3853134 (UMLS CUI [1,2])
English Language comprehension
Item
understand spoken english
boolean
C0376245 (UMLS CUI [1,1])
C0233733 (UMLS CUI [1,2])
Home Telephone Has
Item
have a home telephone
boolean
C0442519 (UMLS CUI [1,1])
C0039457 (UMLS CUI [1,2])
C3539897 (UMLS CUI [1,3])
Clinical Trial Enrollment Household member
Item
no other member of the household enrolled in the study
boolean
C0008976 (UMLS CUI [1,1])
C1516879 (UMLS CUI [1,2])
C0020052 (UMLS CUI [1,3])
C0680022 (UMLS CUI [1,4])
Item Group
C0680251 (UMLS CUI)
Hypertensive disease Cause Secondary
Item
an identified secondary cause of hypertension
boolean
C0020538 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0175668 (UMLS CUI [1,3])
Myocardial Infarction Symptomatic | Cerebrovascular accident
Item
symptomatic myocardial infarction or stroke within the past 6 months
boolean
C0027051 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0038454 (UMLS CUI [2])
Congestive heart failure | New York Heart Association Classification
Item
congestive heart failure (nyha class iii or greater)
boolean
C0018802 (UMLS CUI [1])
C1275491 (UMLS CUI [2])
Renal Insufficiency Significant
Item
significant renal impairment
boolean
C1565489 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Disease Resulting in Cessation of life
Item
diseases likely to lead to noncardiovascular death over the course of the study
boolean
C0012634 (UMLS CUI [1,1])
C0332294 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,3])
Relocation of home Evidence
Item
evidence that the patient may move from the study area before the completion of the study
boolean
C2699029 (UMLS CUI [1,1])
C3887511 (UMLS CUI [1,2])
medical condition Excludes participation | Diagnosis, Psychiatric | Physical disability
Item
presence of any health condition that would preclude participation (e.g., psychiatric diagnosis or physical disability)
boolean
C3843040 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
C0376338 (UMLS CUI [2])
C0520817 (UMLS CUI [3])
Drug usage
Item
active drug use
boolean
C0242510 (UMLS CUI [1])
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