ID

23178

Description

Responsible Party: Technische Universität München ClinicalTrials.gov Identifier: NCT01921036 History of Changes Other Study ID Numbers: 2931/10 DRKS00003625 ( Registry Identifier: German Clinical Trials Register ) Study First Received: July 5, 2013 Last Updated: January 22, 2015 The Effects of Combined Exercise Training on Exercise Capacity in Cardiac Rehabilitation; ODM derived from: https://clinicaltrials.gov/show/NCT01921036

Link

https://clinicaltrials.gov/show/NCT01921036

Keywords

Versions (1)
  1. 6/26/17 6/26/17 -
Uploaded on

June 26, 2017

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License

Creative Commons BY 4.0
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Eligibility Coronary Artery Disease DRKS00003625 NCT01921036 DRKS00003625

English

Eligibility Coronary Artery Disease NCT01921036 DRKS00003625

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
Participation in cardiac rehabilitation
Description

Cardiac rehabilitation

Data type

boolean

Alias
UMLS CUI [1]
C0700431
Written consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
< 1.4 watt/kgbw exercise capacity not more than 12 weeks before study begin
Description

Ergometry

Data type

boolean

Alias
UMLS CUI [1]
C0085143
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
>= 1.4 watt/kgbw
Description

Ergometry: High Intense

Data type

boolean

Alias
UMLS CUI [1,1]
C0085143
UMLS CUI [1,2]
C0205250
contraindications to exercise participation
Description

Contraindication to exercise

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0015259
hospitalized for cvd within six weeks of inclusion
Description

Hospitalized for cvd

Data type

boolean

Alias
UMLS CUI [1,1]
C0184666
UMLS CUI [1,2]
C0007222
acute illness/injury (e.g. fever)
Description

Acute illness

Data type

boolean

Alias
UMLS CUI [1]
C4061114
chronic drug abuse
Description

Substance Use Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0038586
inability to understand study instructions
Description

Understanding Ability

Data type

boolean

Alias
UMLS CUI [1]
C0582778
unwillingness to participate
Description

Unwilling

Data type

boolean

Alias
UMLS CUI [1]
C0558080
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Similar models

Eligibility Coronary Artery Disease NCT01921036 DRKS00003625

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Cardiac rehabilitation
Item
Participation in cardiac rehabilitation
boolean
C0700431 (UMLS CUI [1])
Informed Consent
Item
Written consent
boolean
C0021430 (UMLS CUI [1])
Ergometry
Item
< 1.4 watt/kgbw exercise capacity not more than 12 weeks before study begin
boolean
C0085143 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Ergometry: High Intense
Item
>= 1.4 watt/kgbw
boolean
C0085143 (UMLS CUI [1,1])
C0205250 (UMLS CUI [1,2])
Contraindication to exercise
Item
contraindications to exercise participation
boolean
C1301624 (UMLS CUI [1,1])
C0015259 (UMLS CUI [1,2])
Hospitalized for cvd
Item
hospitalized for cvd within six weeks of inclusion
boolean
C0184666 (UMLS CUI [1,1])
C0007222 (UMLS CUI [1,2])
Acute illness
Item
acute illness/injury (e.g. fever)
boolean
C4061114 (UMLS CUI [1])
Substance Use Disorder
Item
chronic drug abuse
boolean
C0038586 (UMLS CUI [1])
Understanding Ability
Item
inability to understand study instructions
boolean
C0582778 (UMLS CUI [1])
Unwilling
Item
unwillingness to participate
boolean
C0558080 (UMLS CUI [1])
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