Informatie:
Fout:
ID
23552
Beschrijving
Pain in Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT00581724
Link
https://clinicaltrials.gov/show/NCT00581724
Trefwoorden
Versies (1)
- 08-07-17 08-07-17 -
Geüploaded op
8 juli 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00581724
Eligibility Breast Cancer NCT00581724
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00581724
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
cancer treatment
Item
cancer treatment at mskcc
boolean
C0920425 (UMLS CUI [1])
Treatment completed Status post
Item
are from 1 to 10 years post-treatment completion at the time of study recruitment
boolean
C0580352 (UMLS CUI [1,1])
C0231290 (UMLS CUI [1,2])
C0231290 (UMLS CUI [1,2])
Disease Evidence Absent
Item
no evidence of disease (ned) at the time of assessment;
boolean
C0012634 (UMLS CUI [1,1])
C3887511 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C3887511 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Age
Item
over 18 years of age
boolean
C0001779 (UMLS CUI [1])
Telephone Availability of
Item
can be reached by telephone
boolean
C0039457 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C0470187 (UMLS CUI [1,2])
Informed Consent
Item
able to provide informed consent
boolean
C0021430 (UMLS CUI [1])
Able to speak English Language | Able to read English Language
Item
able to speak and read english
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0376245 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
Cancer Survivor | Adjuvant therapy | Patient Self-Report Cancer treatment Type Duration
Item
cancer survivors who received adjuvant therapies outside mskcc will be asked to self-report the type and duration of cancer treatments received.
boolean
C1516231 (UMLS CUI [1])
C0677850 (UMLS CUI [2])
C0681906 (UMLS CUI [3,1])
C0920425 (UMLS CUI [3,2])
C0332307 (UMLS CUI [3,3])
C0449238 (UMLS CUI [3,4])
C0677850 (UMLS CUI [2])
C0681906 (UMLS CUI [3,1])
C0920425 (UMLS CUI [3,2])
C0332307 (UMLS CUI [3,3])
C0449238 (UMLS CUI [3,4])
Cancer treatment | Tamoxifen | Hormone replacement therapy | Biological Factors
Item
undergoing active cancer treatment (ongoing tamoxifen use, hormone replacement therapy or use of biologics are permitted)
boolean
C0920425 (UMLS CUI [1])
C0039286 (UMLS CUI [2])
C0282402 (UMLS CUI [3])
C0005515 (UMLS CUI [4])
C0039286 (UMLS CUI [2])
C0282402 (UMLS CUI [3])
C0005515 (UMLS CUI [4])
Encephalopathy | Psychotic Disorders | Impaired cognition Excludes Informed Consent | Impaired cognition Excludes Surveys Completion
Item
evidence of encephalopathy, psychotic illness or cognitive impairment severe enough to preclude giving informed consent to the study staff, or completing the survey instruments of the study.
boolean
C0085584 (UMLS CUI [1])
C0033975 (UMLS CUI [2])
C0338656 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C0021430 (UMLS CUI [3,3])
C0338656 (UMLS CUI [4,1])
C0332196 (UMLS CUI [4,2])
C0038951 (UMLS CUI [4,3])
C0205197 (UMLS CUI [4,4])
C0033975 (UMLS CUI [2])
C0338656 (UMLS CUI [3,1])
C0332196 (UMLS CUI [3,2])
C0021430 (UMLS CUI [3,3])
C0338656 (UMLS CUI [4,1])
C0332196 (UMLS CUI [4,2])
C0038951 (UMLS CUI [4,3])
C0205197 (UMLS CUI [4,4])