ID

14252

Beskrivning

A Randomized Trial of Changing Exercise and Physical Activity Behavior in Asthma Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00195117

Länk

https://clinicaltrials.gov/show/NCT00195117

Nyckelord

  1. 2016-04-05 2016-04-05 -
Rättsinnehavare

CC BY-NC 3.0

Uppladdad den

5 april 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Asthma NCT00195117

Eligibility Asthma NCT00195117

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00195117
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients will be eligible for this study
Beskrivning

ID.1

Datatyp

boolean

if their physicians consider them medically able to participate, if they are 18 years of age or older
Beskrivning

able to participate

Datatyp

boolean

Alias
UMLS CUI [1]
C1321605
UMLS CUI [2]
C0001779
if they have a diagnosis of mild to moderate asthma based on the nhlbi asthma expert panel's classification system which rates symptoms, frequency of exacerbations, nocturnal attacks, activity restriction, use of medications, and pulmonary function.
Beskrivning

asthma

Datatyp

boolean

Alias
UMLS CUI [1]
C0004096
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients will be excluded from this study for the following reasons:
Beskrivning

ID.4

Datatyp

boolean

if they are unable to walk several blocks for whatever reason;
Beskrivning

walking

Datatyp

boolean

Alias
UMLS CUI [1]
C0080331
if they have musculoskeletal or neurological deficits that preclude increased physical activity;
Beskrivning

comorbidity

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
if they have other pulmonary diseases;
Beskrivning

pulmonary diseases

Datatyp

boolean

Alias
UMLS CUI [1]
C0024115
if they have cardiac disease or other severe comorbidity;
Beskrivning

comorbidity

Datatyp

boolean

Alias
UMLS CUI [1]
C0009488
if they are unable to provide informed consent because of cognitive deficits;
Beskrivning

unable to provide informed consent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
if they refuse to participate.
Beskrivning

refuse to participate

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Asthma NCT00195117

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00195117
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients will be eligible for this study
boolean
able to participate
Item
if their physicians consider them medically able to participate, if they are 18 years of age or older
boolean
C1321605 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
asthma
Item
if they have a diagnosis of mild to moderate asthma based on the nhlbi asthma expert panel's classification system which rates symptoms, frequency of exacerbations, nocturnal attacks, activity restriction, use of medications, and pulmonary function.
boolean
C0004096 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.4
Item
patients will be excluded from this study for the following reasons:
boolean
walking
Item
if they are unable to walk several blocks for whatever reason;
boolean
C0080331 (UMLS CUI [1])
comorbidity
Item
if they have musculoskeletal or neurological deficits that preclude increased physical activity;
boolean
C0009488 (UMLS CUI [1])
pulmonary diseases
Item
if they have other pulmonary diseases;
boolean
C0024115 (UMLS CUI [1])
comorbidity
Item
if they have cardiac disease or other severe comorbidity;
boolean
C0009488 (UMLS CUI [1])
unable to provide informed consent
Item
if they are unable to provide informed consent because of cognitive deficits;
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
refuse to participate
Item
if they refuse to participate.
boolean
C2348568 (UMLS CUI [1])

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