Eligibility High Blood Pressure NCT01622400

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
man or woman of more than 18 years with a health insurance policy
Description

Age | Health Insurance

Data type

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0021682
general practice patients who are agree to participate of the program of patient's therapeutic education in lille (59) or arras (62)
Description

General practice Patients | Participation Education Therapeutic

Data type

boolean

Alias
UMLS CUI [1,1]
C0086343
UMLS CUI [1,2]
C0030705
UMLS CUI [2,1]
C0679823
UMLS CUI [2,2]
C0030688
UMLS CUI [2,3]
C0302350
written informed consent must be obtained prior to performing any study-specific procedures
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
patient at high cardiovascular risk (patient with a high blood pressure and 3 cardiovascular risk factors and/or patient with cardiovascular disease)
Description

Cardiovascular risk High | Hypertensive disease | Cardiovascular risk factor Quantity | Cardiovascular Diseases

Data type

boolean

Alias
UMLS CUI [1,1]
C4324389
UMLS CUI [1,2]
C0205250
UMLS CUI [2]
C0020538
UMLS CUI [3,1]
C0850624
UMLS CUI [3,2]
C1265611
UMLS CUI [4]
C0007222
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient unwilling to take part to the therapeutic education program or to the study
Description

Education Therapeutic Unwilling | Study Subject Participation Status Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C0030688
UMLS CUI [1,2]
C0302350
UMLS CUI [1,3]
C0558080
UMLS CUI [2,1]
C2348568
UMLS CUI [2,2]
C0558080
patient not suitable to participate in the therapeutic education program
Description

Patient Inappropriate Education Therapeutic

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1548788
UMLS CUI [1,3]
C0030688
UMLS CUI [1,4]
C0302350
patient with dementia
Description

Dementia

Data type

boolean

Alias
UMLS CUI [1]
C0497327
anticipated survival (due to comorbidities) of less than one year from baseline
Description

Life Expectancy Due to Comorbidity

Data type

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0009488
patient with current addiction or current alcohol / drug abuse
Description

Addictive Behavior | Substance Use Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0085281
UMLS CUI [2]
C0038586
patient with known plans to move to another area of the country
Description

Relocation of home Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C2699029
UMLS CUI [1,2]
C1301732
unable to obtain written informed consent
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
patient who are pregnant or lactating
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
person without liberty by administrative or judiciary decision
Description

Persons Deprivation Freedom

Data type

boolean

Alias
UMLS CUI [1,1]
C0027361
UMLS CUI [1,2]
C0871712
UMLS CUI [1,3]
C0016694

Similar models

Eligibility High Blood Pressure NCT01622400

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age | Health Insurance
Item
man or woman of more than 18 years with a health insurance policy
boolean
C0001779 (UMLS CUI [1])
C0021682 (UMLS CUI [2])
General practice Patients | Participation Education Therapeutic
Item
general practice patients who are agree to participate of the program of patient's therapeutic education in lille (59) or arras (62)
boolean
C0086343 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0679823 (UMLS CUI [2,1])
C0030688 (UMLS CUI [2,2])
C0302350 (UMLS CUI [2,3])
Informed Consent
Item
written informed consent must be obtained prior to performing any study-specific procedures
boolean
C0021430 (UMLS CUI [1])
Cardiovascular risk High | Hypertensive disease | Cardiovascular risk factor Quantity | Cardiovascular Diseases
Item
patient at high cardiovascular risk (patient with a high blood pressure and 3 cardiovascular risk factors and/or patient with cardiovascular disease)
boolean
C4324389 (UMLS CUI [1,1])
C0205250 (UMLS CUI [1,2])
C0020538 (UMLS CUI [2])
C0850624 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0007222 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Education Therapeutic Unwilling | Study Subject Participation Status Unwilling
Item
patient unwilling to take part to the therapeutic education program or to the study
boolean
C0030688 (UMLS CUI [1,1])
C0302350 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C2348568 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Patient Inappropriate Education Therapeutic
Item
patient not suitable to participate in the therapeutic education program
boolean
C0030705 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0030688 (UMLS CUI [1,3])
C0302350 (UMLS CUI [1,4])
Dementia
Item
patient with dementia
boolean
C0497327 (UMLS CUI [1])
Life Expectancy Due to Comorbidity
Item
anticipated survival (due to comorbidities) of less than one year from baseline
boolean
C0023671 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Addictive Behavior | Substance Use Disorders
Item
patient with current addiction or current alcohol / drug abuse
boolean
C0085281 (UMLS CUI [1])
C0038586 (UMLS CUI [2])
Relocation of home Planned
Item
patient with known plans to move to another area of the country
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Informed Consent Unable
Item
unable to obtain written informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
patient who are pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Persons Deprivation Freedom
Item
person without liberty by administrative or judiciary decision
boolean
C0027361 (UMLS CUI [1,1])
C0871712 (UMLS CUI [1,2])
C0016694 (UMLS CUI [1,3])