Information:
Fel:
ID
43568
Beskrivning
Study of Symptoms Caused by Cancer and Cancer Therapy in Patients With Invasive Breast, Lung, Prostate, or Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00303914
Länk
https://clinicaltrials.gov/show/NCT00303914
Nyckelord
Versioner (2)
- 2017-01-11 2017-01-11 -
- 2021-09-20 2021-09-20 -
Uppladdad den
20 september 2021
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00303914
Eligibility Breast Cancer NCT00303914
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00303914
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Outpatient
Item
being seen in an outpatient setting at an ecog-affiliated academic institution, a cgop site, or a ccop site
boolean
C0029921 (UMLS CUI [1])
Pretreatment Malignant Neoplasm | cancer treatment | follow-up Malignant Neoplasm
Item
in pretreatment, active treatment, or follow-up for their cancer
boolean
C3539076 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
C0920425 (UMLS CUI [2])
C1522577 (UMLS CUI [3,1])
C0006826 (UMLS CUI [3,2])
C0006826 (UMLS CUI [1,2])
C0920425 (UMLS CUI [2])
C1522577 (UMLS CUI [3,1])
C0006826 (UMLS CUI [3,2])
invasive cancer
Item
clinically diagnosed invasive cancer involving at least 1 of the following primary sites:
boolean
C0677898 (UMLS CUI [1])
Breast
Item
breast
boolean
C0006141 (UMLS CUI [1])
Lung
Item
lung
boolean
C0024109 (UMLS CUI [1])
Prostate
Item
prostate
boolean
C0033572 (UMLS CUI [1])
Colorectal
Item
colorectal
boolean
C0555952 (UMLS CUI [1])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C3829127 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,2])
Survey Written Completion
Item
willing to complete a written survey between day 28 and day 35 after completion of the baseline assessment
boolean
C0038951 (UMLS CUI [1,1])
C1547186 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
C1547186 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Able to read English Language | Able to write English Language | Comprehension English Language
Item
able to read, write, and understand english
boolean
C0586740 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0584993 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0233733 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
C0376245 (UMLS CUI [1,2])
C0584993 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0233733 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
Impaired cognition Limiting Responses
Item
no significantly impaired cognitive status which, in the opinion of the investigator, would hinder ability to provide responses
boolean
C0338656 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0871261 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0871261 (UMLS CUI [1,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Unspecified
Item
not specified
boolean
C0205370 (UMLS CUI [1])