Informatie:
Fout:
ID
43591
Beschrijving
Printed Education Materials in Patients Who Are Finishing Treatment for Stage I, Stage II, or Stage IIIA Breast Cancer, Colorectal Cancer, Prostate Cancer, or Chest Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00372840
Link
https://clinicaltrials.gov/show/NCT00372840
Trefwoorden
Versies (2)
- 13-01-17 13-01-17 -
- 20-09-21 20-09-21 -
Geüploaded op
20 september 2021
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00372840
Eligibility Breast Cancer NCT00372840
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00372840
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Breast Carcinoma | Colorectal Carcinoma | Prostate carcinoma | Malignant neoplasm of thorax
Item
diagnosis of breast, colorectal, prostate, or thoracic cancer*
boolean
C0678222 (UMLS CUI [1])
C0009402 (UMLS CUI [2])
C0600139 (UMLS CUI [3])
C0153661 (UMLS CUI [4])
C0009402 (UMLS CUI [2])
C0600139 (UMLS CUI [3])
C0153661 (UMLS CUI [4])
TNM clinical staging
Item
stage i-iii disease
boolean
C3258246 (UMLS CUI [1])
Chemotherapy | Therapeutic radiology procedure | Malignant neoplasm of thorax TNM clinical staging | Mesothelioma | Small cell carcinoma of lung Tumor stage Limited
Item
approaching, attending, or already attended with the past 28 days, the last treatment appointment of chemotherapy and/or radiotherapy note: *stage iiia disease for thoracic cancer and excluded mesothelioma; if small cell lung cancer is present must be limited stage disease
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C0153661 (UMLS CUI [3,1])
C3258246 (UMLS CUI [3,2])
C0025500 (UMLS CUI [4])
C0149925 (UMLS CUI [5,1])
C1300072 (UMLS CUI [5,2])
C0439801 (UMLS CUI [5,3])
C1522449 (UMLS CUI [2])
C0153661 (UMLS CUI [3,1])
C3258246 (UMLS CUI [3,2])
C0025500 (UMLS CUI [4])
C0149925 (UMLS CUI [5,1])
C1300072 (UMLS CUI [5,2])
C0439801 (UMLS CUI [5,3])
Primary malignant neoplasm Quantity
Item
no more than 1 primary cancer
boolean
C1306459 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,2])
Recurrent disease
Item
no recurrent disease
boolean
C0277556 (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])
Able to speak English Language Grade Level | Able to read English Language Grade Level
Item
able to speak/read english at an 8th grade level
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0870612 (UMLS CUI [1,3])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0870612 (UMLS CUI [2,3])
C0376245 (UMLS CUI [1,2])
C0870612 (UMLS CUI [1,3])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0870612 (UMLS CUI [2,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
disease characteristic
Item
see disease characteristics
boolean
C0599878 (UMLS CUI [1])
Brachytherapy
Item
no prior brachytherapy only
boolean
C0006098 (UMLS CUI [1])
Operative Surgical Procedure | Adjuvant therapy
Item
no prior surgery only (i.e., must have received prior adjuvant therapy and surgery)
boolean
C0543467 (UMLS CUI [1])
C0677850 (UMLS CUI [2])
C0677850 (UMLS CUI [2])