ID

23552

Descripción

Pain in Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT00581724

Link

https://clinicaltrials.gov/show/NCT00581724

Palabras clave

  1. 8/7/17 8/7/17 -
Subido en

8 de julio de 2017

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00581724

Eligibility Breast Cancer NCT00581724

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
cancer treatment at mskcc
Descripción

cancer treatment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0920425
are from 1 to 10 years post-treatment completion at the time of study recruitment
Descripción

Treatment completed Status post

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0580352
UMLS CUI [1,2]
C0231290
no evidence of disease (ned) at the time of assessment;
Descripción

Disease Evidence Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3887511
UMLS CUI [1,3]
C0332197
over 18 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
can be reached by telephone
Descripción

Telephone Availability of

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0039457
UMLS CUI [1,2]
C0470187
able to provide informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
able to speak and read english
Descripción

Able to speak English Language | Able to read English Language

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0586740
UMLS CUI [2,2]
C0376245
cancer survivors who received adjuvant therapies outside mskcc will be asked to self-report the type and duration of cancer treatments received.
Descripción

Cancer Survivor | Adjuvant therapy | Patient Self-Report Cancer treatment Type Duration

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1516231
UMLS CUI [2]
C0677850
UMLS CUI [3,1]
C0681906
UMLS CUI [3,2]
C0920425
UMLS CUI [3,3]
C0332307
UMLS CUI [3,4]
C0449238
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
undergoing active cancer treatment (ongoing tamoxifen use, hormone replacement therapy or use of biologics are permitted)
Descripción

Cancer treatment | Tamoxifen | Hormone replacement therapy | Biological Factors

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0920425
UMLS CUI [2]
C0039286
UMLS CUI [3]
C0282402
UMLS CUI [4]
C0005515
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.
Descripción

Encephalopathy | Psychotic Disorders | Impaired cognition Excludes Informed Consent | Impaired cognition Excludes Surveys Completion

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0085584
UMLS CUI [2]
C0033975
UMLS CUI [3,1]
C0338656
UMLS CUI [3,2]
C0332196
UMLS CUI [3,3]
C0021430
UMLS CUI [4,1]
C0338656
UMLS CUI [4,2]
C0332196
UMLS CUI [4,3]
C0038951
UMLS CUI [4,4]
C0205197

Similar models

Eligibility Breast Cancer NCT00581724

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])

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