ID

12565

Description

Emergency Department (ED)-Directed Interventions to Improve Asthma Outcomes; ODM derived from: https://clinicaltrials.gov/show/NCT01079000

Link

https://clinicaltrials.gov/show/NCT01079000

Keywords

Versions (1)
  1. 11/30/15 11/30/15 -
Uploaded on

November 30, 2015

DOI

To request one please log in.

License

Creative Commons BY 4.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Acute Asthma NCT01079000

English

Eligibility Acute Asthma NCT01079000

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 17-55 years old;
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients treated and discharged from one of the four study sites with acute asthma during the study period;
Description

(not simply for a prescription refill)

Data type

boolean

Alias
UMLS CUI [1,1]
C0349790
UMLS CUI [1,2]
C0019993
patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician (e.g., past asthma history, recorded response to β-agonists in the ed, and increased asthma symptoms). in the event of a new diagnosis, the patient is still eligible for the study if the treating physician feels that the history is compatible with a diagnosis of asthma;
Description

patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician

Data type

boolean

Alias
UMLS CUI [1]
C0262926
UMLS CUI [2]
C0004096
UMLS CUI [3]
C0349790
patients must have evidence of airflow obstruction on presentation at the ed, defined as an fev1 or pef <80 percent of predicted;
Description

evidence of airflow obstruction on presentation at the ed

Data type

boolean

Alias
UMLS CUI [1]
C1527303
patients must not have a history of more than 20 pack-years of smoking;
Description

patients must not have a history of more than 20 pack-years of smoking

Data type

boolean

Alias
UMLS CUI [1]
C0038586
all patients should have a pcp with whom to follow-up or attempts will be made to find one for them.
Description

(fp, nurse practitioner or internist)

Data type

boolean

Alias
UMLS CUI [1]
C0033131
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
these criteria ensure the exclusion of suspected copd patients and patients who require different treatments:
Description

suspected copd patients and patients who require different treatments

Data type

boolean

Alias
UMLS CUI [1]
C0024117
patients with asthma who are primarily cared for by a respirologist/pulmonologist;
Description

patients with asthma who are primarily cared for by a respirologist/pulmonologist

Data type

boolean

Alias
UMLS CUI [1]
C0421318
patients not seen by an emergency physician in the ed
Description

(e.g., direct referrals)

Data type

boolean

Alias
UMLS CUI [1]
C2065341
physician diagnosis of acute copd
Description

(e.g., failure of fev1 or pef to respond to ed treatment and a fev1/fvc ratio ≤ 70%);

Data type

boolean

Alias
UMLS CUI [1]
C0340044
radiologically confirmed pneumonia during the 10 days preceding trial entry;
Description

radiologically confirmed pneumonia

Data type

boolean

Alias
UMLS CUI [1]
C3843750
patients with an active history of bronchiectasis, cystic fibrosis, or lung cancer;
Description

active history of bronchiectasis, cystic fibrosis, or lung cancer

Data type

boolean

Alias
UMLS CUI [1]
C0006267
UMLS CUI [2]
C0010674
UMLS CUI [3]
C0242379
clinically confirmed congestive heart failure at ed presentation;
Description

congestive heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0018802
patients not able/unwilling to perform spirometry assessment
Description

patients not able/unwilling to perform spirometry assessment

Data type

boolean

Alias
UMLS CUI [1]
C1321605
UMLS CUI [2]
C0037981
inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
Description

inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;

Data type

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488
patient has previously participated in the study;
Description

patient has previously participated in the study;

Data type

boolean

Alias
UMLS CUI [1]
C2348568
patients who in the opinion of the investigator are unsuitable for enrolment.
Description

patients who in the opinion of the investigator are unsuitable for enrolment.

Data type

boolean

Alias
UMLS CUI [1]
C1321605
Back to the top of the page

Similar models

Eligibility Acute Asthma NCT01079000

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age 17-55 years old;
boolean
C0001779 (UMLS CUI [1])
patients treated and discharged from one of the four study sites with acute asthma during the study period;
Item
patients treated and discharged from one of the four study sites with acute asthma during the study period;
boolean
C0349790 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician
Item
patients must have had a previous physician-diagnosis of asthma and an exacerbation diagnosed by the ed physician (e.g., past asthma history, recorded response to β-agonists in the ed, and increased asthma symptoms). in the event of a new diagnosis, the patient is still eligible for the study if the treating physician feels that the history is compatible with a diagnosis of asthma;
boolean
C0262926 (UMLS CUI [1])
C0004096 (UMLS CUI [2])
C0349790 (UMLS CUI [3])
evidence of airflow obstruction on presentation at the ed
Item
patients must have evidence of airflow obstruction on presentation at the ed, defined as an fev1 or pef <80 percent of predicted;
boolean
C1527303 (UMLS CUI [1])
patients must not have a history of more than 20 pack-years of smoking
Item
patients must not have a history of more than 20 pack-years of smoking;
boolean
C0038586 (UMLS CUI [1])
all patients should have a Primary care physician
Item
all patients should have a pcp with whom to follow-up or attempts will be made to find one for them.
boolean
C0033131 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
suspected copd patients and patients who require different treatments
Item
these criteria ensure the exclusion of suspected copd patients and patients who require different treatments:
boolean
C0024117 (UMLS CUI [1])
patients with asthma who are primarily cared for by a respirologist/pulmonologist
Item
patients with asthma who are primarily cared for by a respirologist/pulmonologist;
boolean
C0421318 (UMLS CUI [1])
patients not seen by an emergency physician
Item
patients not seen by an emergency physician in the ed
boolean
C2065341 (UMLS CUI [1])
physician diagnosis of acute copd
Item
physician diagnosis of acute copd
boolean
C0340044 (UMLS CUI [1])
radiologically confirmed pneumonia
Item
radiologically confirmed pneumonia during the 10 days preceding trial entry;
boolean
C3843750 (UMLS CUI [1])
active history of bronchiectasis, cystic fibrosis, or lung cancer
Item
patients with an active history of bronchiectasis, cystic fibrosis, or lung cancer;
boolean
C0006267 (UMLS CUI [1])
C0010674 (UMLS CUI [2])
C0242379 (UMLS CUI [3])
congestive heart failure
Item
clinically confirmed congestive heart failure at ed presentation;
boolean
C0018802 (UMLS CUI [1])
patients not able/unwilling to perform spirometry assessment
Item
patients not able/unwilling to perform spirometry assessment
boolean
C1321605 (UMLS CUI [1])
C0037981 (UMLS CUI [2])
inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
Item
inability to provide informed consent or comply with the study protocol due to cognitive impairment, language barrier, or no contact details;
boolean
C0021430 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
patient has previously participated in the study;
Item
patient has previously participated in the study;
boolean
C2348568 (UMLS CUI [1])
patients who in the opinion of the investigator are unsuitable for enrolment.
Item
patients who in the opinion of the investigator are unsuitable for enrolment.
boolean
C1321605 (UMLS CUI [1])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial