ID

21477

Beschreibung

Monitoring Asthma and COPD in Primary Care; ODM derived from: https://clinicaltrials.gov/show/NCT00542061

Link

https://clinicaltrials.gov/show/NCT00542061

Stichworte

Versionen (1)
  1. 24.04.17 24.04.17 -
Hochgeladen am

24. April 2017

DOI

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Creative Commons BY 4.0
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Eligibility Lung Diseases, Obstructive NCT00542061

Englisch

Eligibility Lung Diseases, Obstructive NCT00542061

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
the patient is categorised as asthmatic disease with persistent airway obstruction or copd in the monitoring system shl confirmed by the most recent lung function assessment (fev1/fvc < 70% after bd and fev1 ≥ 50% pred after bd) or (fev1 < 80% predicted after bd and ≥ 9% reversibility)
Beschreibung

Asthma | Airway Obstruction persistent | COPD | Monitoring System Lung | Pulmonary function test | FEV1/FVC post bronchodilator | FEV1 post bronchodilator | Disease reversibility Percentage

Datentyp

boolean

Alias
UMLS CUI [1]
C0004096
UMLS CUI [2,1]
C0001883
UMLS CUI [2,2]
C0205322
UMLS CUI [3]
C0024117
UMLS CUI [4,1]
C1139730
UMLS CUI [4,2]
C0024109
UMLS CUI [5]
C0024119
UMLS CUI [6,1]
C3815113
UMLS CUI [6,2]
C2599594
UMLS CUI [7,1]
C0748133
UMLS CUI [7,2]
C2599594
UMLS CUI [8,1]
C0679253
UMLS CUI [8,2]
C0439165
the patient is monitored by the ac service of the shl.
Beschreibung

Monitoring System Lung

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1139730
UMLS CUI [1,2]
C0024109
the gp of the patient is willing to participate in the trial.
Beschreibung

Study Subject Participation Status Willing

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0600109
written informed consent of participant
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients treated primary by a pulmonologist
Beschreibung

Therapeutic procedure Pulmonologist

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0586859
patients currently participating in another respiratory intervention study
Beschreibung

Study Subject Participation Status | Clinical Trial Intervention respiratory

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C0184661
UMLS CUI [2,3]
C0521346
when the gp considers it detrimental to the patient to participate in the study
Beschreibung

Study Subject Participation Status Unfavorable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C3640815
serious other non-pulmonary diseases (or disease-stages) that are presumed to lead to "lost to follow-up" because of the severity of the disease course (like diseases with low survival rate or mental deterioration)
Beschreibung

Disease Serious Follow-up Limited | Disease stage Follow-up Limited | Survival Rate low | Mental deterioration

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C3274571
UMLS CUI [1,4]
C0439801
UMLS CUI [2,1]
C0699749
UMLS CUI [2,2]
C3274571
UMLS CUI [2,3]
C0439801
UMLS CUI [3,1]
C0038954
UMLS CUI [3,2]
C0205251
UMLS CUI [4]
C0234985
serious other pulmonary diseases that effect bronchial symptoms and/or lung function, e.g. sarcoidosis, lung cancer, lung fibrosis
Beschreibung

Lung diseases Serious Causing Symptoms Bronchial | Lung diseases Serious Affecting Lung function | Sarcoidosis | Carcinoma of lung | Pulmonary Fibrosis

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0024115
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0678227
UMLS CUI [1,4]
C1457887
UMLS CUI [1,5]
C0205039
UMLS CUI [2,1]
C0024115
UMLS CUI [2,2]
C0205404
UMLS CUI [2,3]
C0392760
UMLS CUI [2,4]
C0035245
UMLS CUI [3]
C0036202
UMLS CUI [4]
C0684249
UMLS CUI [5]
C0034069
illiteracy
Beschreibung

Illiteracy

Datentyp

boolean

Alias
UMLS CUI [1]
C0020899
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Ähnliche Modelle

Eligibility Lung Diseases, Obstructive NCT00542061

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Asthma | Airway Obstruction persistent | COPD | Monitoring System Lung | Pulmonary function test | FEV1/FVC post bronchodilator | FEV1 post bronchodilator | Disease reversibility Percentage
Item
the patient is categorised as asthmatic disease with persistent airway obstruction or copd in the monitoring system shl confirmed by the most recent lung function assessment (fev1/fvc < 70% after bd and fev1 ≥ 50% pred after bd) or (fev1 < 80% predicted after bd and ≥ 9% reversibility)
boolean
C0004096 (UMLS CUI [1])
C0001883 (UMLS CUI [2,1])
C0205322 (UMLS CUI [2,2])
C0024117 (UMLS CUI [3])
C1139730 (UMLS CUI [4,1])
C0024109 (UMLS CUI [4,2])
C0024119 (UMLS CUI [5])
C3815113 (UMLS CUI [6,1])
C2599594 (UMLS CUI [6,2])
C0748133 (UMLS CUI [7,1])
C2599594 (UMLS CUI [7,2])
C0679253 (UMLS CUI [8,1])
C0439165 (UMLS CUI [8,2])
Monitoring System Lung
Item
the patient is monitored by the ac service of the shl.
boolean
C1139730 (UMLS CUI [1,1])
C0024109 (UMLS CUI [1,2])
Study Subject Participation Status Willing
Item
the gp of the patient is willing to participate in the trial.
boolean
C2348568 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent of participant
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Therapeutic procedure Pulmonologist
Item
patients treated primary by a pulmonologist
boolean
C0087111 (UMLS CUI [1,1])
C0586859 (UMLS CUI [1,2])
Study Subject Participation Status | Clinical Trial Intervention respiratory
Item
patients currently participating in another respiratory intervention study
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])
C0521346 (UMLS CUI [2,3])
Study Subject Participation Status Unfavorable
Item
when the gp considers it detrimental to the patient to participate in the study
boolean
C2348568 (UMLS CUI [1,1])
C3640815 (UMLS CUI [1,2])
Disease Serious Follow-up Limited | Disease stage Follow-up Limited | Survival Rate low | Mental deterioration
Item
serious other non-pulmonary diseases (or disease-stages) that are presumed to lead to "lost to follow-up" because of the severity of the disease course (like diseases with low survival rate or mental deterioration)
boolean
C0012634 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,4])
C0699749 (UMLS CUI [2,1])
C3274571 (UMLS CUI [2,2])
C0439801 (UMLS CUI [2,3])
C0038954 (UMLS CUI [3,1])
C0205251 (UMLS CUI [3,2])
C0234985 (UMLS CUI [4])
Lung diseases Serious Causing Symptoms Bronchial | Lung diseases Serious Affecting Lung function | Sarcoidosis | Carcinoma of lung | Pulmonary Fibrosis
Item
serious other pulmonary diseases that effect bronchial symptoms and/or lung function, e.g. sarcoidosis, lung cancer, lung fibrosis
boolean
C0024115 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0678227 (UMLS CUI [1,3])
C1457887 (UMLS CUI [1,4])
C0205039 (UMLS CUI [1,5])
C0024115 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0392760 (UMLS CUI [2,3])
C0035245 (UMLS CUI [2,4])
C0036202 (UMLS CUI [3])
C0684249 (UMLS CUI [4])
C0034069 (UMLS CUI [5])
Illiteracy
Item
illiteracy
boolean
C0020899 (UMLS CUI [1])
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