ID

20872

Beschreibung

Health E Heart Study (South Texas Veterans Health Care System Heart Failure Disease Management Program/Study); ODM derived from: https://clinicaltrials.gov/show/NCT00141856

Link

https://clinicaltrials.gov/show/NCT00141856

Stichworte

Versionen (1)
  1. 23.03.17 23.03.17 -
Hochgeladen am

23. März 2017

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Heart Failure, Congestive NCT00141856

Englisch

Eligibility Heart Failure, Congestive NCT00141856

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
inclusion criteria are designed to enroll a population of va patients with moderate-severe heart failure who are expected to be reasonably representative of and generalizable to potential candidates for the health e heart disease management program intervention. to be eligible for the study, veteran beneficiaries must:
Beschreibung

Heart failure Moderate | Heart failure Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205081
UMLS CUI [2,1]
C0018801
UMLS CUI [2,2]
C0205082
be 18 years of age
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
have a diagnosis of heart failure
Beschreibung

Heart failure

Datentyp

boolean

Alias
UMLS CUI [1]
C0018801
have received care in urgent care or have been hospitalized, or have more than 12 outpatient visits in the last twelve months.
Beschreibung

Patient care Urgent Care Clinic/Center | Hospitalization | Outpatient visit Quantity

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0017313
UMLS CUI [1,2]
C1551285
UMLS CUI [2]
C0019993
UMLS CUI [3,1]
C0545084
UMLS CUI [3,2]
C1265611
speak either english or spanish.
Beschreibung

Able to speak English Language | Able to speak Spanish Language

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0564215
UMLS CUI [2,2]
C0037750
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
exclusion criteria are designed to exclude persons who are unable to participate in the intervention, whose mortality or health care utilization are driven by co-morbid conditions, or who are enrolled in other research.
Beschreibung

Interventional procedure Participation Unable | Co-morbid conditions | Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0184661
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C1299582
UMLS CUI [2]
C1275743
UMLS CUI [3]
C2348568
end-stage renal disease on chronic dialysis
Beschreibung

Kidney Failure, Chronic | dialysis chronic

Datentyp

boolean

Alias
UMLS CUI [1]
C0022661
UMLS CUI [2]
C0743165
prior heart transplant
Beschreibung

Heart Transplantation

Datentyp

boolean

Alias
UMLS CUI [1]
C0018823
end-stage or terminal illness in addition to heart failure, such as metastatic malignancy or aids with anticipated life expectancy less than 6 months.
Beschreibung

Terminal illness In addition to Heart failure | Metastatic Neoplasm | Acquired Immunodeficiency Syndrome | Life Expectancy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0679247
UMLS CUI [1,2]
C0332287
UMLS CUI [1,3]
C0018801
UMLS CUI [2]
C2939420
UMLS CUI [3]
C0001175
UMLS CUI [4]
C0023671
residence in a nursing home
Beschreibung

nursing home resident

Datentyp

boolean

Alias
UMLS CUI [1]
C0682287
currently participating in another research or care management program.
Beschreibung

Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
no access to a telephone
Beschreibung

Access to telephone Missing

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1822200
UMLS CUI [1,2]
C1705492
severe dementia
Beschreibung

Severe dementia

Datentyp

boolean

Alias
UMLS CUI [1]
C3494652
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Ähnliche Modelle

Eligibility Heart Failure, Congestive NCT00141856

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Heart failure Moderate | Heart failure Severe
Item
inclusion criteria are designed to enroll a population of va patients with moderate-severe heart failure who are expected to be reasonably representative of and generalizable to potential candidates for the health e heart disease management program intervention. to be eligible for the study, veteran beneficiaries must:
boolean
C0018801 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0018801 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Age
Item
be 18 years of age
boolean
C0001779 (UMLS CUI [1])
Heart failure
Item
have a diagnosis of heart failure
boolean
C0018801 (UMLS CUI [1])
Patient care Urgent Care Clinic/Center | Hospitalization | Outpatient visit Quantity
Item
have received care in urgent care or have been hospitalized, or have more than 12 outpatient visits in the last twelve months.
boolean
C0017313 (UMLS CUI [1,1])
C1551285 (UMLS CUI [1,2])
C0019993 (UMLS CUI [2])
C0545084 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
Able to speak English Language | Able to speak Spanish Language
Item
speak either english or spanish.
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0564215 (UMLS CUI [2,1])
C0037750 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Interventional procedure Participation Unable | Co-morbid conditions | Study Subject Participation Status
Item
exclusion criteria are designed to exclude persons who are unable to participate in the intervention, whose mortality or health care utilization are driven by co-morbid conditions, or who are enrolled in other research.
boolean
C0184661 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C1275743 (UMLS CUI [2])
C2348568 (UMLS CUI [3])
Kidney Failure, Chronic | dialysis chronic
Item
end-stage renal disease on chronic dialysis
boolean
C0022661 (UMLS CUI [1])
C0743165 (UMLS CUI [2])
Heart Transplantation
Item
prior heart transplant
boolean
C0018823 (UMLS CUI [1])
Terminal illness In addition to Heart failure | Metastatic Neoplasm | Acquired Immunodeficiency Syndrome | Life Expectancy
Item
end-stage or terminal illness in addition to heart failure, such as metastatic malignancy or aids with anticipated life expectancy less than 6 months.
boolean
C0679247 (UMLS CUI [1,1])
C0332287 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
C2939420 (UMLS CUI [2])
C0001175 (UMLS CUI [3])
C0023671 (UMLS CUI [4])
nursing home resident
Item
residence in a nursing home
boolean
C0682287 (UMLS CUI [1])
Study Subject Participation Status
Item
currently participating in another research or care management program.
boolean
C2348568 (UMLS CUI [1])
Access to telephone Missing
Item
no access to a telephone
boolean
C1822200 (UMLS CUI [1,1])
C1705492 (UMLS CUI [1,2])
Severe dementia
Item
severe dementia
boolean
C3494652 (UMLS CUI [1])
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