Eligibility Breast Cancer NCT00712569

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject inclusion criteria for patients
Descrizione

Inclusion criteria Patients

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0030705
female
Descrizione

Gender

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0079399
diagnosis of breast cancer
Descrizione

Breast Carcinoma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0678222
pre-surgery (*for breast surgeon patients only)
Descrizione

pre-surgery

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0441943
report that they have read breast cancer-related internet information since their diagnosis with breast cancer.
Descrizione

Internet Information Breast Carcinoma Related

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0282111
UMLS CUI [1,2]
C1533716
UMLS CUI [1,3]
C0678222
UMLS CUI [1,4]
C0439849
provide informed consent
Descrizione

Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
subject inclusion criteria physicians
Descrizione

Inclusion criteria Physicians

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0031831
breast surgeon or breast medical oncologist
Descrizione

Breast surgeon | Breast oncologist

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0586886
UMLS CUI [2,1]
C0006141
UMLS CUI [2,2]
C0259990
agree to participate in study and one of 10 selected participants
Descrizione

Agreement Participation Clinical Trial

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0680240
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0008976
provide inform consent
Descrizione

Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
exclusion criteria for patients
Descrizione

Exclusion Criteria Patients

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0030705
less than 21 years of age
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
cognitive or physical impairment rendering patients incapable of providing informed consent to participate in the study
Descrizione

Impaired cognition Informed Consent Unable | Physical impairment Informed Consent Unable

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0338656
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C0231171
UMLS CUI [2,2]
C0021430
UMLS CUI [2,3]
C1299582
as the measures and coding system are all written in english, subjects who are not fluent in english will be excluded.
Descrizione

Lacking Ability to speak fluently English Language

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0564240
UMLS CUI [1,3]
C0376245
exclusion criteria for physicians
Descrizione

Exclusion Criteria Physicians

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0031831
none
Descrizione

None

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0549184

Similar models

Eligibility Breast Cancer NCT00712569

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Inclusion criteria Patients
Item
subject inclusion criteria for patients
boolean
C1512693 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Breast Carcinoma
Item
diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
pre-surgery
Item
pre-surgery (*for breast surgeon patients only)
boolean
C0441943 (UMLS CUI [1])
Internet Information Breast Carcinoma Related
Item
report that they have read breast cancer-related internet information since their diagnosis with breast cancer.
boolean
C0282111 (UMLS CUI [1,1])
C1533716 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
C0439849 (UMLS CUI [1,4])
Informed Consent
Item
provide informed consent
boolean
C0021430 (UMLS CUI [1])
Inclusion criteria Physicians
Item
subject inclusion criteria physicians
boolean
C1512693 (UMLS CUI [1,1])
C0031831 (UMLS CUI [1,2])
Breast surgeon | Breast oncologist
Item
breast surgeon or breast medical oncologist
boolean
C0586886 (UMLS CUI [1])
C0006141 (UMLS CUI [2,1])
C0259990 (UMLS CUI [2,2])
Agreement Participation Clinical Trial
Item
agree to participate in study and one of 10 selected participants
boolean
C0680240 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Informed Consent
Item
provide inform consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Exclusion Criteria Patients
Item
exclusion criteria for patients
boolean
C0680251 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
Age
Item
less than 21 years of age
boolean
C0001779 (UMLS CUI [1])
Impaired cognition Informed Consent Unable | Physical impairment Informed Consent Unable
Item
cognitive or physical impairment rendering patients incapable of providing informed consent to participate in the study
boolean
C0338656 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0231171 (UMLS CUI [2,1])
C0021430 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
Lacking Ability to speak fluently English Language
Item
as the measures and coding system are all written in english, subjects who are not fluent in english will be excluded.
boolean
C0332268 (UMLS CUI [1,1])
C0564240 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
Exclusion Criteria Physicians
Item
exclusion criteria for physicians
boolean
C0680251 (UMLS CUI [1,1])
C0031831 (UMLS CUI [1,2])
None
Item
none
boolean
C0549184 (UMLS CUI [1])