ID

33301

Beskrivning

Effectiveness of an Interdisciplinary, Nurse-coordinated Atrial Fibrillation Expert Program for Primary Care Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01928121

Länk

https://clinicaltrials.gov/show/NCT01928121

Nyckelord

  1. 2018-12-05 2018-12-05 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

5 december 2018

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT01928121

Eligibility Atrial Fibrillation NCT01928121

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
every newly diagnosed af patient.
Beskrivning

Atrial Fibrillation

Datatyp

boolean

Alias
UMLS CUI [1]
C0004238
every af patient who is not seen by a cardiologist or electrophysiologist in the past 2 years before inclusion.
Beskrivning

Atrial Fibrillation | Seen by cardiologist Lacking

Datatyp

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0583557
UMLS CUI [2,2]
C0332268
af must be confirmed on electrocardiogram.
Beskrivning

Atrial Fibrillation Electrocardiogram

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C1623258
capable of providing written informed consent.
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
dutch speaking and verbally testable, without cognitive impairment.
Beskrivning

Able to speak Dutch Language | Impaired cognition Absent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376241
UMLS CUI [2,1]
C0338656
UMLS CUI [2,2]
C0332197
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
af patients who once received an arrhythmologic consult about af prior to the start of the study.
Beskrivning

Atrial Fibrillation | Consult Arrhythmia Received

Datatyp

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0009818
UMLS CUI [2,2]
C0003811
UMLS CUI [2,3]
C1514756
af patients who have a systematic follow-up at a cardiologist prior to the start of the study.
Beskrivning

Atrial Fibrillation | Follow-up systematic Cardiologist

Datatyp

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C1522577
UMLS CUI [2,2]
C0220922
UMLS CUI [2,3]
C0175906
terminally ill af patients
Beskrivning

Atrial Fibrillation Terminal illness

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0679247
participation in another clinical trial
Beskrivning

Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Atrial Fibrillation NCT01928121

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Atrial Fibrillation
Item
every newly diagnosed af patient.
boolean
C0004238 (UMLS CUI [1])
Atrial Fibrillation | Seen by cardiologist Lacking
Item
every af patient who is not seen by a cardiologist or electrophysiologist in the past 2 years before inclusion.
boolean
C0004238 (UMLS CUI [1])
C0583557 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
Atrial Fibrillation Electrocardiogram
Item
af must be confirmed on electrocardiogram.
boolean
C0004238 (UMLS CUI [1,1])
C1623258 (UMLS CUI [1,2])
Informed Consent
Item
capable of providing written informed consent.
boolean
C0021430 (UMLS CUI [1])
Able to speak Dutch Language | Impaired cognition Absent
Item
dutch speaking and verbally testable, without cognitive impairment.
boolean
C0564215 (UMLS CUI [1,1])
C0376241 (UMLS CUI [1,2])
C0338656 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Atrial Fibrillation | Consult Arrhythmia Received
Item
af patients who once received an arrhythmologic consult about af prior to the start of the study.
boolean
C0004238 (UMLS CUI [1])
C0009818 (UMLS CUI [2,1])
C0003811 (UMLS CUI [2,2])
C1514756 (UMLS CUI [2,3])
Atrial Fibrillation | Follow-up systematic Cardiologist
Item
af patients who have a systematic follow-up at a cardiologist prior to the start of the study.
boolean
C0004238 (UMLS CUI [1])
C1522577 (UMLS CUI [2,1])
C0220922 (UMLS CUI [2,2])
C0175906 (UMLS CUI [2,3])
Atrial Fibrillation Terminal illness
Item
terminally ill af patients
boolean
C0004238 (UMLS CUI [1,1])
C0679247 (UMLS CUI [1,2])
Study Subject Participation Status
Item
participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])

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