ID

14298

Beschrijving

Efficacy of Mobile Phone Short Message Service (SMS) Reminder and Consultation on Asthma Control; ODM derived from: https://clinicaltrials.gov/show/NCT02189616

Link

https://clinicaltrials.gov/show/NCT02189616

Trefwoorden

  1. 07-04-16 07-04-16 -
Geüploaded op

7 april 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Asthma NCT02189616

Eligibility Asthma NCT02189616

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT02189616
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. physician diagnosed uncontrolled or partly-controlled asthma by global initiative for asthma(gina) standard.
Beschrijving

Uncontrolled Asthma | Asthma Control function Partial

Datatype

boolean

Alias
UMLS CUI [1,1]
C0205318
UMLS CUI [1,2]
C0004096
UMLS CUI [2,1]
C0004096
UMLS CUI [2,2]
C2587213
UMLS CUI [2,3]
C0728938
2. at least 6 months asthma history.
Beschrijving

Asthma

Datatype

boolean

Alias
UMLS CUI [1]
C0004096
3. ownership of a mobile phone and currently using the text messaging service.
Beschrijving

Ownership Mobile Phone | Text Messaging

Datatype

boolean

Alias
UMLS CUI [1,1]
C0029981
UMLS CUI [1,2]
C1136360
UMLS CUI [2]
C3178908
4. age between 18 and 65 years old.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
5. willingness to participate in this study.
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
6. willing to sign the written informed consent to take part in the study.
Beschrijving

Informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. inability to provide written informed consent or to fill in the paper asthma diary.
Beschrijving

Unable Informed Consent | Unable Fill Out Form Asthma Diaries

Datatype

boolean

Alias
UMLS CUI [1,1]
C1299582
UMLS CUI [1,2]
C0021430
UMLS CUI [2,1]
C1299582
UMLS CUI [2,2]
C3273494
UMLS CUI [2,3]
C0004096
UMLS CUI [2,4]
C0376660
2. a history of smoking cigarettes for greater than ten pack years.
Beschrijving

smoking cigarettes: ____ pack-years history

Datatype

boolean

Alias
UMLS CUI [1]
C2230126
3. other current or a history of severe comorbidity.
Beschrijving

Severe comorbidity

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
4. being in other clinical trials.
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Asthma NCT02189616

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT02189616
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Uncontrolled Asthma | Asthma Control function Partial
Item
1. physician diagnosed uncontrolled or partly-controlled asthma by global initiative for asthma(gina) standard.
boolean
C0205318 (UMLS CUI [1,1])
C0004096 (UMLS CUI [1,2])
C0004096 (UMLS CUI [2,1])
C2587213 (UMLS CUI [2,2])
C0728938 (UMLS CUI [2,3])
Asthma
Item
2. at least 6 months asthma history.
boolean
C0004096 (UMLS CUI [1])
Ownership Mobile Phone | Text Messaging
Item
3. ownership of a mobile phone and currently using the text messaging service.
boolean
C0029981 (UMLS CUI [1,1])
C1136360 (UMLS CUI [1,2])
C3178908 (UMLS CUI [2])
Age
Item
4. age between 18 and 65 years old.
boolean
C0001779 (UMLS CUI [1])
Study Subject Participation Status
Item
5. willingness to participate in this study.
boolean
C2348568 (UMLS CUI [1])
Informed consent
Item
6. willing to sign the written informed consent to take part in the study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Unable Informed Consent | Unable Fill Out Form Asthma Diaries
Item
1. inability to provide written informed consent or to fill in the paper asthma diary.
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1299582 (UMLS CUI [2,1])
C3273494 (UMLS CUI [2,2])
C0004096 (UMLS CUI [2,3])
C0376660 (UMLS CUI [2,4])
smoking cigarettes: ____ pack-years history
Item
2. a history of smoking cigarettes for greater than ten pack years.
boolean
C2230126 (UMLS CUI [1])
Severe comorbidity
Item
3. other current or a history of severe comorbidity.
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Study Subject Participation Status
Item
4. being in other clinical trials.
boolean
C2348568 (UMLS CUI [1])

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