ID

12998

Description

Randomized Trial of Follow-up Strategies in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00156039

Link

https://clinicaltrials.gov/show/NCT00156039

Keywords

Versions (1)
  1. 1/10/16 1/10/16 -
Uploaded on

January 10, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00156039

English

Eligibility Breast Cancer NCT00156039

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
women with breast cancer on well follow-up at regional cancer centres in ontario and manitoba
Description

Gender, breast cancer, follow up

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0678222
UMLS CUI [3]
C1522577
diagnosed at least 12 months previously (range 9-15 months)
Description

date of diagnosis

Data type

boolean

Alias
UMLS CUI [1,1]
C2316983
UMLS CUI [1,2]
C1274082
without evidence of active disease (i.e., stages iiib and iv excluded)
Description

no active disease

Data type

boolean

Alias
UMLS CUI [1]
C2707252
free from any primary treatment complications
Description

treatment complications

Data type

boolean

Alias
UMLS CUI [1]
C0679861
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
primary treatment at least 3 months previously, except for continued use of tamoxifen
Description

primary treatment date, tamoxifen

Data type

boolean

Alias
UMLS CUI [1,1]
C1708063
UMLS CUI [1,2]
C0011008
UMLS CUI [2]
C0039286
still experiencing complications of primary treatment (patients will become eligible once complications resolve provided they are within the 6 month window)
Description

complications of primary treatment

Data type

boolean

Alias
UMLS CUI [1]
C0679861
UMLS CUI [2]
C1708063
unable to identify an acceptable family physician to provide follow-up
Description

family physician to provide follow-up

Data type

boolean

Alias
UMLS CUI [1]
C1522577
language or literacy skills inconsistent with completing questionnaires
Description

language

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C1145677
unable to comply with study protocol including completion of questionnaires
Description

unable to comply

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
previously enrolled in a study which requires continued follow-up in specialist or peripheral clinics
Description

study participation status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
actively followed at a cancer centre for another primary cancer
Description

malignancies

Data type

boolean

Alias
UMLS CUI [1]
C0006826
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Similar models

Eligibility Breast Cancer NCT00156039

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender, breast cancer, follow up
Item
women with breast cancer on well follow-up at regional cancer centres in ontario and manitoba
boolean
C0079399 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
C1522577 (UMLS CUI [3])
date of diagnosis
Item
diagnosed at least 12 months previously (range 9-15 months)
boolean
C2316983 (UMLS CUI [1,1])
C1274082 (UMLS CUI [1,2])
no active disease
Item
without evidence of active disease (i.e., stages iiib and iv excluded)
boolean
C2707252 (UMLS CUI [1])
treatment complications
Item
free from any primary treatment complications
boolean
C0679861 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
primary treatment date, tamoxifen
Item
primary treatment at least 3 months previously, except for continued use of tamoxifen
boolean
C1708063 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0039286 (UMLS CUI [2])
complications of primary treatment
Item
still experiencing complications of primary treatment (patients will become eligible once complications resolve provided they are within the 6 month window)
boolean
C0679861 (UMLS CUI [1])
C1708063 (UMLS CUI [2])
family physician to provide follow-up
Item
unable to identify an acceptable family physician to provide follow-up
boolean
C1522577 (UMLS CUI [1])
language
Item
language or literacy skills inconsistent with completing questionnaires
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1145677 (UMLS CUI [1,3])
unable to comply
Item
unable to comply with study protocol including completion of questionnaires
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
study participation status
Item
previously enrolled in a study which requires continued follow-up in specialist or peripheral clinics
boolean
C2348568 (UMLS CUI [1])
malignancies
Item
actively followed at a cancer centre for another primary cancer
boolean
C0006826 (UMLS CUI [1])
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