Informationen:
Fehler:
ID
35579
Beschreibung
VIDA Mobile Health Cardiovascular Prevention Program; ODM derived from: https://clinicaltrials.gov/show/NCT02431546
Link
https://clinicaltrials.gov/show/NCT02431546
Stichworte
Versionen (1)
- 10.03.19 10.03.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
10. März 2019
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT02431546
Eligibility Coronary Artery Disease NCT02431546
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Coronary Artery Disease NCT02431546
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
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])
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])
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])
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])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
Symptoms Coronary Artery Disease
Item
acute symptoms of coronary artery disease
boolean
C1457887 (UMLS CUI [1,1])
C1956346 (UMLS CUI [1,2])
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])
C0205082 (UMLS CUI [1,2])
Pulmonary Hypertension Severe
Item
severe pulmonary hypertension
boolean
C0020542 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])