ID

14511

Description

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

Lien

https://clinicaltrials.gov/show/NCT02509130

Mots-clés

  1. 19/04/2016 19/04/2016 -
Téléchargé le

19 avril 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Asthma NCT02509130

Eligibility Asthma NCT02509130

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

Inclusion Criteria

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

Age

Type de données

boolean

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

Population Group

Type de données

boolean

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

Rapid Access Asthma clinic

Type de données

boolean

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

Severe asthma Assessment Clinic

Type de données

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
Description

Uncontrolled Asthma | Primary Care

Type de données

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 -
Description

Referral to asthma clinic

Type de données

boolean

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

Severe asthma Outpatients

Type de données

boolean

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

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

Type de données

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.
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

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

Unable Informed Consent

Type de données

boolean

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

Similar models

Eligibility Asthma NCT02509130

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT02509130
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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