Information:
Fel:
ID
39879
Beskrivning
Efficacy of a Dedicated Therapeutic Education Program in Patients at High Cardiovascular Risk; ODM derived from: https://clinicaltrials.gov/show/NCT01622400
Länk
https://clinicaltrials.gov/show/NCT01622400
Nyckelord
Versioner (1)
- 2020-02-27 2020-02-27 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
27 februari 2020
DOI
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Licens
Creative Commons BY 4.0
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Eligibility High Blood Pressure NCT01622400
Eligibility High Blood Pressure NCT01622400
- StudyEvent: Eligibility
Similar models
Eligibility High Blood Pressure NCT01622400
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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])
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])
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])
C0205250 (UMLS CUI [1,2])
C0020538 (UMLS CUI [2])
C0850624 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0007222 (UMLS CUI [4])
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])
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])
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])
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])
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])
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])
C1299582 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
patient who are pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
C0871712 (UMLS CUI [1,2])
C0016694 (UMLS CUI [1,3])