ID

44543

Beschrijving

Self-Management and Care of Heart Failure With Group Clinics (SMAC-HF); ODM derived from: https://clinicaltrials.gov/show/NCT00439842

Link

https://clinicaltrials.gov/show/NCT00439842

Trefwoorden

Versies (2)
  1. 06-04-18 06-04-18 -
  2. 27-09-21 27-09-21 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

27 september 2021

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Heart Failure, Congestive NCT00439842

Engels

Eligibility Heart Failure, Congestive NCT00439842

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
18 years or older
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
speak english/spanish
Beschrijving

Able to speak English Language | Able to speak Spanish Language

Datatype

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0564215
UMLS CUI [2,2]
C0037750
receiving treatment for congestive heart failure
Beschrijving

Therapeutic procedure Congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0018802
receiving iv diuretics
Beschrijving

Diuretics Intravenous

Datatype

boolean

Alias
UMLS CUI [1,1]
C0012798
UMLS CUI [1,2]
C1522726
2 or more hf symptoms
Beschrijving

Symptoms Quantity Heart failure

Datatype

boolean

Alias
UMLS CUI [1,1]
C1457887
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0018801
be able to participate in follow up visits
Beschrijving

Ability Participation Follow-up visit

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0589121
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
primary right-sided heart failure
Beschrijving

Right-Sided Heart Failure Primary

Datatype

boolean

Alias
UMLS CUI [1,1]
C0235527
UMLS CUI [1,2]
C0205225
hf transient & related to acute mi
Beschrijving

Heart failure Transient | Relationship Myocardial Infarction

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205374
UMLS CUI [2,1]
C0439849
UMLS CUI [2,2]
C0027051
hf due to correctable cause
Beschrijving

Heart failure Due to Cause Reversible

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0015127
UMLS CUI [1,4]
C0205343
being scheduled for coronary revascularization or any readmission
Beschrijving

Coronary revascularisation Scheduled | Patient Readmission Scheduled

Datatype

boolean

Alias
UMLS CUI [1,1]
C0877341
UMLS CUI [1,2]
C0205539
UMLS CUI [2,1]
C0030700
UMLS CUI [2,2]
C0205539
receiving infusion for hf therapy within 2 weeks
Beschrijving

Infusion care Heart failure

Datatype

boolean

Alias
UMLS CUI [1,1]
C2958553
UMLS CUI [1,2]
C0018801
having co-morbidities, life expectancy < 12 months
Beschrijving

Comorbidity | Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C0023671
severe cognitive impairment
Beschrijving

Severe cognitive impairment

Datatype

boolean

Alias
UMLS CUI [1]
C3554639
d/c to nursing facilities or rehab unit
Beschrijving

Patient Discharge Destination Nursing facility | Patient Discharge Destination Rehabilitation unit

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030685
UMLS CUI [1,2]
C0079220
UMLS CUI [1,3]
C3258821
UMLS CUI [2,1]
C0030685
UMLS CUI [2,2]
C0079220
UMLS CUI [2,3]
C1550688
currently enrolled in an intervention study or hf management program
Beschrijving

Study Subject Participation Status | Clinical Trial Interventional procedure | Management program Heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C0184661
UMLS CUI [3,1]
C1303150
UMLS CUI [3,2]
C0018801
being or planning to become pregnant within 12 months
Beschrijving

Pregnancy | Pregnancy, Planned

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
severe cognitive impairment
Beschrijving

Severe cognitive impairment

Datatype

boolean

Alias
UMLS CUI [1]
C3554639
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Similar models

Eligibility Heart Failure, Congestive NCT00439842

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
18 years or older
boolean
C0001779 (UMLS CUI [1])
Able to speak English Language | Able to speak Spanish Language
Item
speak english/spanish
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0564215 (UMLS CUI [2,1])
C0037750 (UMLS CUI [2,2])
Therapeutic procedure Congestive heart failure
Item
receiving treatment for congestive heart failure
boolean
C0087111 (UMLS CUI [1,1])
C0018802 (UMLS CUI [1,2])
Diuretics Intravenous
Item
receiving iv diuretics
boolean
C0012798 (UMLS CUI [1,1])
C1522726 (UMLS CUI [1,2])
Symptoms Quantity Heart failure
Item
2 or more hf symptoms
boolean
C1457887 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
Ability Participation Follow-up visit
Item
be able to participate in follow up visits
boolean
C0085732 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0589121 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Right-Sided Heart Failure Primary
Item
primary right-sided heart failure
boolean
C0235527 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Heart failure Transient | Relationship Myocardial Infarction
Item
hf transient & related to acute mi
boolean
C0018801 (UMLS CUI [1,1])
C0205374 (UMLS CUI [1,2])
C0439849 (UMLS CUI [2,1])
C0027051 (UMLS CUI [2,2])
Heart failure Due to Cause Reversible
Item
hf due to correctable cause
boolean
C0018801 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0205343 (UMLS CUI [1,4])
Coronary revascularisation Scheduled | Patient Readmission Scheduled
Item
being scheduled for coronary revascularization or any readmission
boolean
C0877341 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C0030700 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Infusion care Heart failure
Item
receiving infusion for hf therapy within 2 weeks
boolean
C2958553 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
Comorbidity | Life Expectancy
Item
having co-morbidities, life expectancy < 12 months
boolean
C0009488 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
Severe cognitive impairment
Item
severe cognitive impairment
boolean
C3554639 (UMLS CUI [1])
Patient Discharge Destination Nursing facility | Patient Discharge Destination Rehabilitation unit
Item
d/c to nursing facilities or rehab unit
boolean
C0030685 (UMLS CUI [1,1])
C0079220 (UMLS CUI [1,2])
C3258821 (UMLS CUI [1,3])
C0030685 (UMLS CUI [2,1])
C0079220 (UMLS CUI [2,2])
C1550688 (UMLS CUI [2,3])
Study Subject Participation Status | Clinical Trial Interventional procedure | Management program Heart failure
Item
currently enrolled in an intervention study or hf management program
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])
C1303150 (UMLS CUI [3,1])
C0018801 (UMLS CUI [3,2])
Pregnancy | Pregnancy, Planned
Item
being or planning to become pregnant within 12 months
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Severe cognitive impairment
Item
severe cognitive impairment
boolean
C3554639 (UMLS CUI [1])
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