ID

23178

Beschrijving

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

Trefwoorden

  1. 26-06-17 26-06-17 -
Geüploaded op

26 juni 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease DRKS00003625 NCT01921036 DRKS00003625

Eligibility Coronary Artery Disease NCT01921036 DRKS00003625

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
Participation in cardiac rehabilitation
Beschrijving

Cardiac rehabilitation

Datatype

boolean

Alias
UMLS CUI [1]
C0700431
Written consent
Beschrijving

Informed Consent

Datatype

boolean

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

Ergometry

Datatype

boolean

Alias
UMLS CUI [1]
C0085143
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
>= 1.4 watt/kgbw
Beschrijving

Ergometry: High Intense

Datatype

boolean

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

Contraindication to exercise

Datatype

boolean

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

Hospitalized for cvd

Datatype

boolean

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

Acute illness

Datatype

boolean

Alias
UMLS CUI [1]
C4061114
chronic drug abuse
Beschrijving

Substance Use Disorder

Datatype

boolean

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

Understanding Ability

Datatype

boolean

Alias
UMLS CUI [1]
C0582778
unwillingness to participate
Beschrijving

Unwilling

Datatype

boolean

Alias
UMLS CUI [1]
C0558080

Similar models

Eligibility Coronary Artery Disease NCT01921036 DRKS00003625

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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