ID

35579

Beschrijving

VIDA Mobile Health Cardiovascular Prevention Program; ODM derived from: https://clinicaltrials.gov/show/NCT02431546

Link

https://clinicaltrials.gov/show/NCT02431546

Trefwoorden

Versies (1)
  1. 10-03-19 10-03-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

10 maart 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT02431546

Engels

Eligibility Coronary Artery Disease NCT02431546

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
graduates of cr, who were originally enrolled in cr following myocardial infarction (mi), percutaneous coronary intervention (pci), or coronary artery bypass graft (cabg) or with stable angina
Beschrijving

Graduate Cardiac rehabilitation | Enrollment Previous Cardiac rehabilitation | Myocardial Infarction | Percutaneous Coronary Intervention | Coronary Artery Bypass Surgery | Stable angina

Datatype

boolean

Alias
UMLS CUI [1,1]
C0588053
UMLS CUI [1,2]
C0700431
UMLS CUI [2,1]
C1516879
UMLS CUI [2,2]
C0205156
UMLS CUI [2,3]
C0700431
UMLS CUI [3]
C0027051
UMLS CUI [4]
C1532338
UMLS CUI [5]
C0010055
UMLS CUI [6]
C0340288
adequate clinical stability has been achieved in the judgment of the investigator to allow participation in study assessments and the intervention
Beschrijving

Study Subject Participation Status Stability Clinical

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C0205210
ability to participate in a mobile health program with access to smartphones utilizing apple and android platforms
Beschrijving

Participation Mobile Health | Access Smartphone

Datatype

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C2718080
UMLS CUI [2,1]
C0444454
UMLS CUI [2,2]
C3204335
signed informed consent document indicating that the patient understands the purpose of and procedures required for the study and is willing to participate in the study
Beschrijving

Informed Consent | Comprehension Study Protocol

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0162340
UMLS CUI [2,2]
C2348563
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
acute symptoms of coronary artery disease
Beschrijving

Symptoms Coronary Artery Disease

Datatype

boolean

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C1956346
decompensated heart failure
Beschrijving

Decompensated cardiac failure

Datatype

boolean

Alias
UMLS CUI [1]
C0581377
severe valvular heart disease
Beschrijving

Heart valve disease Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018824
UMLS CUI [1,2]
C0205082
severe pulmonary hypertension
Beschrijving

Pulmonary Hypertension Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020542
UMLS CUI [1,2]
C0205082
end stage renal disease
Beschrijving

Kidney Failure, Chronic

Datatype

boolean

Alias
UMLS CUI [1]
C0022661
heart failure, new york heart association (nyha) class iv
Beschrijving

Heart failure New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
cardiac transplantation
Beschrijving

Heart Transplantation

Datatype

boolean

Alias
UMLS CUI [1]
C0018823
terminal illness with life expectancy < 1 year
Beschrijving

Terminal illness | Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0679247
UMLS CUI [2]
C0023671
impairment from stroke, injury or other medical disorder that precludes participation in the intervention
Beschrijving

Impairment Due to Cerebrovascular accident | Impairment Due to Injury | Impairment Due to Disease | Participation Intervention Excluded

Datatype

boolean

Alias
UMLS CUI [1,1]
C0221099
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0038454
UMLS CUI [2,1]
C0221099
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C3263723
UMLS CUI [3,1]
C0221099
UMLS CUI [3,2]
C0678226
UMLS CUI [3,3]
C0012634
UMLS CUI [4,1]
C0679823
UMLS CUI [4,2]
C0184661
UMLS CUI [4,3]
C0332196
dementia that precludes ability to participate in and follow study protocols
Beschrijving

Dementia | Protocol Compliance Unable

Datatype

boolean

Alias
UMLS CUI [1]
C0497327
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C1299582
enrollment in a clinical trial not approved for co-enrollment
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
inability or unwillingness to comply with the study requirements
Beschrijving

Protocol Compliance Unable | Protocol Compliance Unwilling

Datatype

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C0558080
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Similar models

Eligibility Coronary Artery Disease NCT02431546

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Graduate Cardiac rehabilitation | Enrollment Previous Cardiac rehabilitation | Myocardial Infarction | Percutaneous Coronary Intervention | Coronary Artery Bypass Surgery | Stable angina
Item
graduates of cr, who were originally enrolled in cr following myocardial infarction (mi), percutaneous coronary intervention (pci), or coronary artery bypass graft (cabg) or with stable angina
boolean
C0588053 (UMLS CUI [1,1])
C0700431 (UMLS CUI [1,2])
C1516879 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C0700431 (UMLS CUI [2,3])
C0027051 (UMLS CUI [3])
C1532338 (UMLS CUI [4])
C0010055 (UMLS CUI [5])
C0340288 (UMLS CUI [6])
Study Subject Participation Status Stability Clinical
Item
adequate clinical stability has been achieved in the judgment of the investigator to allow participation in study assessments and the intervention
boolean
C2348568 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
Participation Mobile Health | Access Smartphone
Item
ability to participate in a mobile health program with access to smartphones utilizing apple and android platforms
boolean
C0679823 (UMLS CUI [1,1])
C2718080 (UMLS CUI [1,2])
C0444454 (UMLS CUI [2,1])
C3204335 (UMLS CUI [2,2])
Informed Consent | Comprehension Study Protocol
Item
signed informed consent document indicating that the patient understands the purpose of and procedures required for the study and is willing to participate in the study
boolean
C0021430 (UMLS CUI [1])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Symptoms Coronary Artery Disease
Item
acute symptoms of coronary artery disease
boolean
C1457887 (UMLS CUI [1,1])
C1956346 (UMLS CUI [1,2])
Decompensated cardiac failure
Item
decompensated heart failure
boolean
C0581377 (UMLS CUI [1])
Heart valve disease Severe
Item
severe valvular heart disease
boolean
C0018824 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Pulmonary Hypertension Severe
Item
severe pulmonary hypertension
boolean
C0020542 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Kidney Failure, Chronic
Item
end stage renal disease
boolean
C0022661 (UMLS CUI [1])
Heart failure New York Heart Association Classification
Item
heart failure, new york heart association (nyha) class iv
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Heart Transplantation
Item
cardiac transplantation
boolean
C0018823 (UMLS CUI [1])
Terminal illness | Life Expectancy
Item
terminal illness with life expectancy < 1 year
boolean
C0679247 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
Impairment Due to Cerebrovascular accident | Impairment Due to Injury | Impairment Due to Disease | Participation Intervention Excluded
Item
impairment from stroke, injury or other medical disorder that precludes participation in the intervention
boolean
C0221099 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0038454 (UMLS CUI [1,3])
C0221099 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C3263723 (UMLS CUI [2,3])
C0221099 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0012634 (UMLS CUI [3,3])
C0679823 (UMLS CUI [4,1])
C0184661 (UMLS CUI [4,2])
C0332196 (UMLS CUI [4,3])
Dementia | Protocol Compliance Unable
Item
dementia that precludes ability to participate in and follow study protocols
boolean
C0497327 (UMLS CUI [1])
C0525058 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Study Subject Participation Status
Item
enrollment in a clinical trial not approved for co-enrollment
boolean
C2348568 (UMLS CUI [1])
Protocol Compliance Unable | Protocol Compliance Unwilling
Item
inability or unwillingness to comply with the study requirements
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
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