ID

14252

Descripción

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

Link

https://clinicaltrials.gov/show/NCT00195117

Palabras clave

  1. 5/4/16 5/4/16 -
Titular de derechos de autor

CC BY-NC 3.0

Subido en

5 de abril de 2016

DOI

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Licencia

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
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

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

able to participate

Tipo de datos

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.
Descripción

asthma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004096
Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.4

Tipo de datos

boolean

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

walking

Tipo de datos

boolean

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

comorbidity

Tipo de datos

boolean

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

pulmonary diseases

Tipo de datos

boolean

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

comorbidity

Tipo de datos

boolean

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

unable to provide informed consent

Tipo de datos

boolean

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

refuse to participate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Asthma NCT00195117

  1. StudyEvent: Eligibility
    1. Eligibility Asthma NCT00195117
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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