ID

18136

Descrizione

Asthma In-Home Monitoring (AIM) Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00282516

collegamento

https://clinicaltrials.gov/show/NCT00282516

Keywords

versioni (1)
  1. 21/10/16 21/10/16 -
Caricato su

21 ottobre 2016

DOI

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Licenza

Creative Commons BY 4.0
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Eligibility Mild, Moderate and Severe Persistent Asthma as Defined by NHLBI-2 Guidelines NCT00282516

Inglese

Eligibility Mild, Moderate and Severe Persistent Asthma as Defined by NHLBI-2 Guidelines NCT00282516

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of persistent asthma as defined using the nhlbi expert panel report -2 guidelines assignment of severity classification will be made at the beginning of the study based on severity of disease off therapy.
Descrizione

Persistent asthma | Degrees of severity

Tipo di dati

boolean

Alias
UMLS CUI [1]
C3266628
UMLS CUI [2]
C0441982
dependent of active duty or retired us military personnel
Descrizione

Military Personnel dependent

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0026126
UMLS CUI [1,2]
C3244310
6 to 17 years of age
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
not moving from oahu for 12 months after entry into study
Descrizione

Relocation of home

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2699029
ability to receive cable modem hook-up in home
Descrizione

modem device Home Ability

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0011007
UMLS CUI [1,2]
C0442519
UMLS CUI [1,3]
C0085732
willingness to learn to record and send mdi + spacer technique and peak flow two times week
Descrizione

Metered Dose Inhaler Readiness to learn | AeroChamber MDI Spacer Readiness to learn | Peak expiratory flow rate measurement Readiness to learn

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0993596
UMLS CUI [1,2]
C1299415
UMLS CUI [2,1]
C0725073
UMLS CUI [2,2]
C1299415
UMLS CUI [3,1]
C0030735
UMLS CUI [3,2]
C1299415
willing to attend asthma education follow-up visits either in person or electronically at 2- weeks, 6- weeks, 3-months and 6-month intervals after initiation into the study.
Descrizione

Asthma education Follow-up visit Willing

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1679754
UMLS CUI [1,2]
C0589121
UMLS CUI [1,3]
C0600109
willing to complete survey at the end of study period.
Descrizione

Survey Completion Willing

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0038951
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C0600109
willing to sign informed, written consent
Descrizione

Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
diagnosis of mild intermittent asthma as defined by expert panel report -2 guidelines.
Descrizione

Mild intermittent asthma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1960045
<6 and >17 years of age
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
family leaving oahu within 12 months
Descrizione

Family Relocation of home

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0015576
UMLS CUI [1,2]
C2699029
inability to receive cable modem hook-up in home
Descrizione

modem device Home Unable

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0011007
UMLS CUI [1,2]
C0442519
UMLS CUI [1,3]
C1299582
unwilling or unable to learn to record and send mdi + spacer technique and peak flow and/or to attend asthma education follow-up visits either in person or electronically at initiation into study and at 2- weeks, 6- weeks, 3-months and 6 month intervals.
Descrizione

Metered Dose Inhaler Learning Unwilling | AeroChamber MDI Spacer Learning Unwilling | Peak expiratory flow rate measurement Learning Unwilling | Asthma education Follow-up visit Unwilling

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0993596
UMLS CUI [1,2]
C0023185
UMLS CUI [1,3]
C0558080
UMLS CUI [2,1]
C0725073
UMLS CUI [2,2]
C0023185
UMLS CUI [2,3]
C0558080
UMLS CUI [3,1]
C0030735
UMLS CUI [3,2]
C0023185
UMLS CUI [3,3]
C0558080
UMLS CUI [4,1]
C1679754
UMLS CUI [4,2]
C0589121
UMLS CUI [4,3]
C0558080
unwilling to complete survey at the end of study period.
Descrizione

Survey Completion Unwilling

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0038951
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C0558080
patients or parents who decline to participate.
Descrizione

participation Refused | parent participation Refused

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C1705116
UMLS CUI [2,1]
C0030551
UMLS CUI [2,2]
C0679823
UMLS CUI [2,3]
C1705116
patients with other chronic pulmonary disease (cystic fibrosis, bronchopulmonary dysplasia)
Descrizione

Other chronic pulmonary disease | Cystic Fibrosis | Bronchopulmonary Dysplasia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0810290
UMLS CUI [2]
C0010674
UMLS CUI [3]
C0006287
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Similar models

Eligibility Mild, Moderate and Severe Persistent Asthma as Defined by NHLBI-2 Guidelines NCT00282516

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Persistent asthma | Degrees of severity
Item
diagnosis of persistent asthma as defined using the nhlbi expert panel report -2 guidelines assignment of severity classification will be made at the beginning of the study based on severity of disease off therapy.
boolean
C3266628 (UMLS CUI [1])
C0441982 (UMLS CUI [2])
Military Personnel dependent
Item
dependent of active duty or retired us military personnel
boolean
C0026126 (UMLS CUI [1,1])
C3244310 (UMLS CUI [1,2])
Age
Item
6 to 17 years of age
boolean
C0001779 (UMLS CUI [1])
Relocation of home
Item
not moving from oahu for 12 months after entry into study
boolean
C2699029 (UMLS CUI [1])
modem device Home Ability
Item
ability to receive cable modem hook-up in home
boolean
C0011007 (UMLS CUI [1,1])
C0442519 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Metered Dose Inhaler Readiness to learn | AeroChamber MDI Spacer Readiness to learn | Peak expiratory flow rate measurement Readiness to learn
Item
willingness to learn to record and send mdi + spacer technique and peak flow two times week
boolean
C0993596 (UMLS CUI [1,1])
C1299415 (UMLS CUI [1,2])
C0725073 (UMLS CUI [2,1])
C1299415 (UMLS CUI [2,2])
C0030735 (UMLS CUI [3,1])
C1299415 (UMLS CUI [3,2])
Asthma education Follow-up visit Willing
Item
willing to attend asthma education follow-up visits either in person or electronically at 2- weeks, 6- weeks, 3-months and 6-month intervals after initiation into the study.
boolean
C1679754 (UMLS CUI [1,1])
C0589121 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
Survey Completion Willing
Item
willing to complete survey at the end of study period.
boolean
C0038951 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
Informed Consent
Item
willing to sign informed, written consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Mild intermittent asthma
Item
diagnosis of mild intermittent asthma as defined by expert panel report -2 guidelines.
boolean
C1960045 (UMLS CUI [1])
Age
Item
<6 and >17 years of age
boolean
C0001779 (UMLS CUI [1])
Family Relocation of home
Item
family leaving oahu within 12 months
boolean
C0015576 (UMLS CUI [1,1])
C2699029 (UMLS CUI [1,2])
modem device Home Unable
Item
inability to receive cable modem hook-up in home
boolean
C0011007 (UMLS CUI [1,1])
C0442519 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Metered Dose Inhaler Learning Unwilling | AeroChamber MDI Spacer Learning Unwilling | Peak expiratory flow rate measurement Learning Unwilling | Asthma education Follow-up visit Unwilling
Item
unwilling or unable to learn to record and send mdi + spacer technique and peak flow and/or to attend asthma education follow-up visits either in person or electronically at initiation into study and at 2- weeks, 6- weeks, 3-months and 6 month intervals.
boolean
C0993596 (UMLS CUI [1,1])
C0023185 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0725073 (UMLS CUI [2,1])
C0023185 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
C0030735 (UMLS CUI [3,1])
C0023185 (UMLS CUI [3,2])
C0558080 (UMLS CUI [3,3])
C1679754 (UMLS CUI [4,1])
C0589121 (UMLS CUI [4,2])
C0558080 (UMLS CUI [4,3])
Survey Completion Unwilling
Item
unwilling to complete survey at the end of study period.
boolean
C0038951 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
participation Refused | parent participation Refused
Item
patients or parents who decline to participate.
boolean
C0679823 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
C0030551 (UMLS CUI [2,1])
C0679823 (UMLS CUI [2,2])
C1705116 (UMLS CUI [2,3])
Other chronic pulmonary disease | Cystic Fibrosis | Bronchopulmonary Dysplasia
Item
patients with other chronic pulmonary disease (cystic fibrosis, bronchopulmonary dysplasia)
boolean
C0810290 (UMLS CUI [1])
C0010674 (UMLS CUI [2])
C0006287 (UMLS CUI [3])
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