Eligibility Coronary Heart Disease NCT00010738

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
able to attend training sessions and meetings
Beschrijving

Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
local residence
Beschrijving

Residence

Datatype

boolean

Alias
UMLS CUI [1]
C0237096
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
comorbid disease precluding survival in group
Beschrijving

Comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
mi, unstable angina, cabg or ptca within last three months.
Beschrijving

Cardiac status

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0010055
UMLS CUI [4]
C2936173
cognitive/psychological/substance abuse impairment
Beschrijving

Cognitive/psychological/substance abuse impairment

Datatype

boolean

Alias
UMLS CUI [1]
C0338656
UMLS CUI [2]
C0004936
UMLS CUI [3]
C0038586
atrial fibrillation, predominant pacemaker rhythm or significant conduction system disease
Beschrijving

Conduction system status

Datatype

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2]
C0232193
UMLS CUI [3]
C0264886
significant valvular heart disease
Beschrijving

Valvular heart disease

Datatype

boolean

Alias
UMLS CUI [1]
C0018824
class iii or iv heart failure
Beschrijving

Heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C1319795
UMLS CUI [2]
C1319796
renal failure
Beschrijving

Renal failure

Datatype

boolean

Alias
UMLS CUI [1]
C0035078
participating in a formal stress management program
Beschrijving

Participation status: stress management program

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0679002
participation in another trial
Beschrijving

Participation status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Coronary Heart Disease NCT00010738

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Compliance
Item
able to attend training sessions and meetings
boolean
C1321605 (UMLS CUI [1])
Residence
Item
local residence
boolean
C0237096 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Comorbidity
Item
comorbid disease precluding survival in group
boolean
C0009488 (UMLS CUI [1])
Cardiac status
Item
mi, unstable angina, cabg or ptca within last three months.
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0010055 (UMLS CUI [3])
C2936173 (UMLS CUI [4])
Cognitive/psychological/substance abuse impairment
Item
cognitive/psychological/substance abuse impairment
boolean
C0338656 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0038586 (UMLS CUI [3])
Conduction system status
Item
atrial fibrillation, predominant pacemaker rhythm or significant conduction system disease
boolean
C0004238 (UMLS CUI [1])
C0232193 (UMLS CUI [2])
C0264886 (UMLS CUI [3])
Valvular heart disease
Item
significant valvular heart disease
boolean
C0018824 (UMLS CUI [1])
Heart failure
Item
class iii or iv heart failure
boolean
C1319795 (UMLS CUI [1])
C1319796 (UMLS CUI [2])
Renal failure
Item
renal failure
boolean
C0035078 (UMLS CUI [1])
Participation status: stress management program
Item
participating in a formal stress management program
boolean
C2348568 (UMLS CUI [1,1])
C0679002 (UMLS CUI [1,2])
Participation status
Item
participation in another trial
boolean
C2348568 (UMLS CUI [1])