ID

20872

Descrizione

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

collegamento

https://clinicaltrials.gov/show/NCT00141856

Keywords

versioni (1)
  1. 23/03/17 23/03/17 -
Caricato su

23 marzo 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Heart Failure, Congestive NCT00141856

Inglese

Eligibility Heart Failure, Congestive NCT00141856

1 moduli  
Inclusion Criteria
Descrizione

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:
Descrizione

Heart failure Moderate | Heart failure Severe

Tipo di dati

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
Descrizione

Age

Tipo di dati

boolean

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

Heart failure

Tipo di dati

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.
Descrizione

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

Tipo di dati

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.
Descrizione

Able to speak English Language | Able to speak Spanish Language

Tipo di dati

boolean

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

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.
Descrizione

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

Tipo di dati

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
Descrizione

Kidney Failure, Chronic | dialysis chronic

Tipo di dati

boolean

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

Heart Transplantation

Tipo di dati

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.
Descrizione

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

Tipo di dati

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
Descrizione

nursing home resident

Tipo di dati

boolean

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

Study Subject Participation Status

Tipo di dati

boolean

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

Access to telephone Missing

Tipo di dati

boolean

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

Severe dementia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C3494652
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Similar models

Eligibility Heart Failure, Congestive NCT00141856

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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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