ID

34236

Descrição

a Bike Application to Support Cardiac Patient; ODM derived from: https://clinicaltrials.gov/show/NCT02470143

Link

https://clinicaltrials.gov/show/NCT02470143

Palavras-chave

  1. 15/01/2019 15/01/2019 -
Titular dos direitos

see on clinicaltrials.gov

Transferido a

15 de janeiro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT02470143

Eligibility Coronary Artery Disease NCT02470143

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with coronary artery disease for which they received a percutaneous coronary intervention, coronary artery bypass grafting or drugs only.
Descrição

ID.1

Tipo de dados

boolean

patients that have completed the standard cardiac rehabilitation program
Descrição

ID.2

Tipo de dados

boolean

patients who have access to a computer and a wifi internet connection
Descrição

ID.3

Tipo de dados

boolean

patients that are able to go to the rehabilitation centre rego of jessa hospital
Descrição

ID.4

Tipo de dados

boolean

patients who signed the informed consent document
Descrição

ID.5

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a history of vf, sustained vt and/or supraventricular tachycardia during the last 6 months before enrollment.
Descrição

ID.6

Tipo de dados

boolean

patients who due to cognitive, neurological and/or musculoskeletal constraints are unable to ride a bicycle.
Descrição

ID.7

Tipo de dados

boolean

patients with a pacemaker.
Descrição

ID.8

Tipo de dados

boolean

non-dutch speaking patients
Descrição

ID.9

Tipo de dados

boolean

patients who simultaneously participate in another study
Descrição

ID.10

Tipo de dados

boolean

Similar models

Eligibility Coronary Artery Disease NCT02470143

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients with coronary artery disease for which they received a percutaneous coronary intervention, coronary artery bypass grafting or drugs only.
boolean
ID.2
Item
patients that have completed the standard cardiac rehabilitation program
boolean
ID.3
Item
patients who have access to a computer and a wifi internet connection
boolean
ID.4
Item
patients that are able to go to the rehabilitation centre rego of jessa hospital
boolean
ID.5
Item
patients who signed the informed consent document
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
patients with a history of vf, sustained vt and/or supraventricular tachycardia during the last 6 months before enrollment.
boolean
ID.7
Item
patients who due to cognitive, neurological and/or musculoskeletal constraints are unable to ride a bicycle.
boolean
ID.8
Item
patients with a pacemaker.
boolean
ID.9
Item
non-dutch speaking patients
boolean
ID.10
Item
patients who simultaneously participate in another study
boolean

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