Eligibility Coronary Artery Disease NCT02470143

Inclusion Criteria
Descripción

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.
Descripción

ID.1

Tipo de datos

boolean

patients that have completed the standard cardiac rehabilitation program
Descripción

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

patients who signed the informed consent document
Descripción

ID.5

Tipo de datos

boolean

Exclusion Criteria
Descripción

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.
Descripción

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

patients with a pacemaker.
Descripción

ID.8

Tipo de datos

boolean

non-dutch speaking patients
Descripción

ID.9

Tipo de datos

boolean

patients who simultaneously participate in another study
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Coronary Artery Disease NCT02470143

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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