ID

27559

Beschrijving

Trial of a Cardiac Rehabilitation Program Delivered Remotely Through the Internet; ODM derived from: https://clinicaltrials.gov/show/NCT00683813

Link

https://clinicaltrials.gov/show/NCT00683813

Trefwoorden

Versies (1)
  1. 20-11-17 20-11-17 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

20 november 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT00683813

Engels

Eligibility Cardiovascular Disease NCT00683813

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. men and women admitted for an ihd event (acute coronary syndrome or revascularization procedure) who are at low or moderate risk.91
Beschrijving

Gender | Myocardial Ischemia Low Risk | Myocardial Ischemia At risk Moderate | Acute Coronary Syndrome | Revascularization

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0151744
UMLS CUI [2,2]
C3538919
UMLS CUI [3,1]
C0151744
UMLS CUI [3,2]
C1444641
UMLS CUI [3,3]
C0205081
UMLS CUI [4]
C0948089
UMLS CUI [5]
C0581603
2. regular internet access (home, work or other environment).
Beschrijving

Internet Access Regular

Datatype

boolean

Alias
UMLS CUI [1,1]
C0282111
UMLS CUI [1,2]
C0444454
UMLS CUI [1,3]
C0205272
3. over 18 years of age.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
4. permission of the attending physician.
Beschrijving

Study Subject Participation Status | Permission Attending physician

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0521104
UMLS CUI [2,2]
C1320929
5. able to read, write and understand english without difficulty.
Beschrijving

Able to read English Language | Able to write English Language | Comprehension English Language

Datatype

boolean

Alias
UMLS CUI [1,1]
C0586740
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0584993
UMLS CUI [2,2]
C0376245
UMLS CUI [3,1]
C0233733
UMLS CUI [3,2]
C0376245
6. no physical limitations to regular activity.
Beschrijving

Physical disability Absent Regular activity

Datatype

boolean

Alias
UMLS CUI [1,1]
C0520817
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0815170
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. previous experience with a cardiac rehabilitation program.
Beschrijving

Cardiac rehabilitation Previous

Datatype

boolean

Alias
UMLS CUI [1,1]
C0700431
UMLS CUI [1,2]
C0205156
2. patients with depression, uncontrolled diabetes and other significant co-morbidities that may interfere with effective ihd management.
Beschrijving

Depressive disorder | Diabetic - poor control | Comorbidity Interferes with Therapeutic procedure Myocardial Ischemia

Datatype

boolean

Alias
UMLS CUI [1]
C0011581
UMLS CUI [2]
C0421258
UMLS CUI [3,1]
C0009488
UMLS CUI [3,2]
C0521102
UMLS CUI [3,3]
C0087111
UMLS CUI [3,4]
C0151744
3. those patients, who in the mind of the attending physician, are unsuitable for participation.
Beschrijving

Study Subject Participation Status Inappropriate

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
4. those unable to provide informed consent.
Beschrijving

Informed Consent Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
5. pregnant women.
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
6. high-risk patients for safety considerations (future studies will include high-risk patients).
Beschrijving

Patients High risk

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0332167
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Similar models

Eligibility Cardiovascular Disease NCT00683813

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Myocardial Ischemia Low Risk | Myocardial Ischemia At risk Moderate | Acute Coronary Syndrome | Revascularization
Item
1. men and women admitted for an ihd event (acute coronary syndrome or revascularization procedure) who are at low or moderate risk.91
boolean
C0079399 (UMLS CUI [1])
C0151744 (UMLS CUI [2,1])
C3538919 (UMLS CUI [2,2])
C0151744 (UMLS CUI [3,1])
C1444641 (UMLS CUI [3,2])
C0205081 (UMLS CUI [3,3])
C0948089 (UMLS CUI [4])
C0581603 (UMLS CUI [5])
Internet Access Regular
Item
2. regular internet access (home, work or other environment).
boolean
C0282111 (UMLS CUI [1,1])
C0444454 (UMLS CUI [1,2])
C0205272 (UMLS CUI [1,3])
Age
Item
3. over 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Study Subject Participation Status | Permission Attending physician
Item
4. permission of the attending physician.
boolean
C2348568 (UMLS CUI [1])
C0521104 (UMLS CUI [2,1])
C1320929 (UMLS CUI [2,2])
Able to read English Language | Able to write English Language | Comprehension English Language
Item
5. able to read, write and understand english without difficulty.
boolean
C0586740 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0584993 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0233733 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
Physical disability Absent Regular activity
Item
6. no physical limitations to regular activity.
boolean
C0520817 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0815170 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Cardiac rehabilitation Previous
Item
1. previous experience with a cardiac rehabilitation program.
boolean
C0700431 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Depressive disorder | Diabetic - poor control | Comorbidity Interferes with Therapeutic procedure Myocardial Ischemia
Item
2. patients with depression, uncontrolled diabetes and other significant co-morbidities that may interfere with effective ihd management.
boolean
C0011581 (UMLS CUI [1])
C0421258 (UMLS CUI [2])
C0009488 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0087111 (UMLS CUI [3,3])
C0151744 (UMLS CUI [3,4])
Study Subject Participation Status Inappropriate
Item
3. those patients, who in the mind of the attending physician, are unsuitable for participation.
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
Informed Consent Unable
Item
4. those unable to provide informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Pregnancy
Item
5. pregnant women.
boolean
C0032961 (UMLS CUI [1])
Patients High risk
Item
6. high-risk patients for safety considerations (future studies will include high-risk patients).
boolean
C0030705 (UMLS CUI [1,1])
C0332167 (UMLS CUI [1,2])
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