ID

39880

Description

Randomized Trial of Tailored Dietary Advice to Lower Blood Pressure; ODM derived from: https://clinicaltrials.gov/show/NCT01689844

Link

https://clinicaltrials.gov/show/NCT01689844

Keywords

Versions (1)
  1. 2/27/20 2/27/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

February 27, 2020

DOI

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License

Creative Commons BY 4.0
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Eligibility High Blood Pressure NCT01689844

English

Eligibility High Blood Pressure NCT01689844

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
must be age 21 or older,
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
have a diagnosis of hypertension or pre-hypertension
Description

Hypertensive disease | Prehypertension

Data type

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C1696708
under regular care with their physician, and
Description

Patient care Regular

Data type

boolean

Alias
UMLS CUI [1,1]
C0017313
UMLS CUI [1,2]
C0205272
compliant with medications.
Description

Medication compliance

Data type

boolean

Alias
UMLS CUI [1]
C2364172
systolic blood pressure of 120-140 mmhg and/or
Description

Systolic Pressure

Data type

boolean

Alias
UMLS CUI [1]
C0871470
a diastolic blood pressure of 80-90 mmhg (average of two visits)
Description

Average diastolic blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C1282163
on stable doses of antihypertensive medications for a minimum of two months prior to randomization, (and for the duration of the study).
Description

Antihypertensive Agents Dose Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
be able to follow all trial procedures.
Description

Adherence Clinical Trial procedures

Data type

boolean

Alias
UMLS CUI [1,1]
C1510802
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0184661
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
cardiovascular event within 6 months,
Description

Cardiovascular event

Data type

boolean

Alias
UMLS CUI [1]
C1320716
chronic disease that might interfere with trial participation (e.g. chronic kidney disease (estimated gfr < 60 cc/min),
Description

Chronic disease Interferes with Study Subject Participation Status | Chronic Kidney Disease | Estimated Glomerular Filtration Rate

Data type

boolean

Alias
UMLS CUI [1,1]
C0008679
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C2348568
UMLS CUI [2]
C1561643
UMLS CUI [3]
C3811844
unwillingness or inability to adopt a dash-like diet, and
Description

DASH Diet Unwilling | DASH Diet Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C4053458
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C4053458
UMLS CUI [2,2]
C1299582
consumption of more than 14 alcoholic drinks per week,
Description

Alcohol consumption Alcohol units per week

Data type

boolean

Alias
UMLS CUI [1,1]
C0001948
UMLS CUI [1,2]
C0560579
poorly controlled diabetes (hemoglobin a1c >9%),
Description

Poorly controlled diabetes mellitus | Hemoglobin A1c measurement

Data type

boolean

Alias
UMLS CUI [1]
C0554876
UMLS CUI [2]
C0474680
use of insulin,
Description

Insulin use

Data type

boolean

Alias
UMLS CUI [1]
C0240016
use of mineral supplements or an unwillingness to stop supplements one month prior to randomization and refrain from the supplements during the study.
Description

Mineral supplements | Mineral supplements Discontinue Unwilling

Data type

boolean

Alias
UMLS CUI [1]
C0556112
UMLS CUI [2,1]
C0556112
UMLS CUI [2,2]
C1444662
UMLS CUI [2,3]
C0558080
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Similar models

Eligibility High Blood Pressure NCT01689844

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
must be age 21 or older,
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease | Prehypertension
Item
have a diagnosis of hypertension or pre-hypertension
boolean
C0020538 (UMLS CUI [1])
C1696708 (UMLS CUI [2])
Patient care Regular
Item
under regular care with their physician, and
boolean
C0017313 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
Medication compliance
Item
compliant with medications.
boolean
C2364172 (UMLS CUI [1])
Systolic Pressure
Item
systolic blood pressure of 120-140 mmhg and/or
boolean
C0871470 (UMLS CUI [1])
Average diastolic blood pressure
Item
a diastolic blood pressure of 80-90 mmhg (average of two visits)
boolean
C1282163 (UMLS CUI [1])
Antihypertensive Agents Dose Stable
Item
on stable doses of antihypertensive medications for a minimum of two months prior to randomization, (and for the duration of the study).
boolean
C0003364 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Adherence Clinical Trial procedures
Item
be able to follow all trial procedures.
boolean
C1510802 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Cardiovascular event
Item
cardiovascular event within 6 months,
boolean
C1320716 (UMLS CUI [1])
Chronic disease Interferes with Study Subject Participation Status | Chronic Kidney Disease | Estimated Glomerular Filtration Rate
Item
chronic disease that might interfere with trial participation (e.g. chronic kidney disease (estimated gfr < 60 cc/min),
boolean
C0008679 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C1561643 (UMLS CUI [2])
C3811844 (UMLS CUI [3])
DASH Diet Unwilling | DASH Diet Unable
Item
unwillingness or inability to adopt a dash-like diet, and
boolean
C4053458 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C4053458 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Alcohol consumption Alcohol units per week
Item
consumption of more than 14 alcoholic drinks per week,
boolean
C0001948 (UMLS CUI [1,1])
C0560579 (UMLS CUI [1,2])
Poorly controlled diabetes mellitus | Hemoglobin A1c measurement
Item
poorly controlled diabetes (hemoglobin a1c >9%),
boolean
C0554876 (UMLS CUI [1])
C0474680 (UMLS CUI [2])
Insulin use
Item
use of insulin,
boolean
C0240016 (UMLS CUI [1])
Mineral supplements | Mineral supplements Discontinue Unwilling
Item
use of mineral supplements or an unwillingness to stop supplements one month prior to randomization and refrain from the supplements during the study.
boolean
C0556112 (UMLS CUI [1])
C0556112 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
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