ID

14511

Beschreibung

MISSION Severe Asthma Modern Innovative Solutions to Improve Outcomes in Severe Asthma.; ODM derived from: https://clinicaltrials.gov/show/NCT02509130

Link

https://clinicaltrials.gov/show/NCT02509130

Stichworte

  1. 19.04.16 19.04.16 -
Hochgeladen am

19. April 2016

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Asthma NCT02509130

Eligibility Asthma NCT02509130

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT02509130
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female, aged 18 years or above.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
is in one of the following population groups:
Beschreibung

Population Group

Datentyp

boolean

Alias
UMLS CUI [1]
C1257890
attended the mission raac or
Beschreibung

Rapid Access Asthma clinic

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0456962
UMLS CUI [1,2]
C0444454
UMLS CUI [1,3]
C3838770
attended the mission saac or
Beschreibung

Severe asthma Assessment Clinic

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0581126
UMLS CUI [1,2]
C0220825
UMLS CUI [1,3]
C0442592
identified as uncontrolled asthma by record searches and invited to mission raac but did not attend - 'primary care patients' or
Beschreibung

Uncontrolled Asthma | Primary Care

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0205318
UMLS CUI [1,2]
C0004096
UMLS CUI [2]
C0033137
has been referred to the specialist asthma clinic at queen alexandra hospital -
Beschreibung

Referral to asthma clinic

Datentyp

boolean

Alias
UMLS CUI [1]
C1532348
'outpatient severe asthma patients' or
Beschreibung

Severe asthma Outpatients

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0581126
UMLS CUI [1,2]
C0029921
attended the mission raac or saac as a health care professional
Beschreibung

Rapid Access Asthma clinic | Severe asthma Assessment Clinic | Health Personnel

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0456962
UMLS CUI [1,2]
C0444454
UMLS CUI [1,3]
C3838770
UMLS CUI [2,1]
C0581126
UMLS CUI [2,2]
C0220825
UMLS CUI [2,3]
C0442592
UMLS CUI [3]
C0018724
participant is willing and able to give informed consent for participation in the study.
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
the patient is unable or unwilling to give consent
Beschreibung

Unable Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1299582
UMLS CUI [1,2]
C0021430

Ähnliche Modelle

Eligibility Asthma NCT02509130

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT02509130
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male or female, aged 18 years or above.
boolean
C0001779 (UMLS CUI [1])
Population Group
Item
is in one of the following population groups:
boolean
C1257890 (UMLS CUI [1])
Rapid Access Asthma clinic
Item
attended the mission raac or
boolean
C0456962 (UMLS CUI [1,1])
C0444454 (UMLS CUI [1,2])
C3838770 (UMLS CUI [1,3])
Severe asthma Assessment Clinic
Item
attended the mission saac or
boolean
C0581126 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0442592 (UMLS CUI [1,3])
Uncontrolled Asthma | Primary Care
Item
identified as uncontrolled asthma by record searches and invited to mission raac but did not attend - 'primary care patients' or
boolean
C0205318 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0033137 (UMLS CUI [2])
Referral to asthma clinic
Item
has been referred to the specialist asthma clinic at queen alexandra hospital -
boolean
C1532348 (UMLS CUI [1])
Severe asthma Outpatients
Item
'outpatient severe asthma patients' or
boolean
C0581126 (UMLS CUI [1,1])
C0029921 (UMLS CUI [1,2])
Rapid Access Asthma clinic | Severe asthma Assessment Clinic | Health Personnel
Item
attended the mission raac or saac as a health care professional
boolean
C0456962 (UMLS CUI [1,1])
C0444454 (UMLS CUI [1,2])
C3838770 (UMLS CUI [1,3])
C0581126 (UMLS CUI [2,1])
C0220825 (UMLS CUI [2,2])
C0442592 (UMLS CUI [2,3])
C0018724 (UMLS CUI [3])
Informed Consent
Item
participant is willing and able to give informed consent for participation in the study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Unable Informed Consent
Item
the patient is unable or unwilling to give consent
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])

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