Information:
Fel:
ID
26304
Beskrivning
Physician-Patient Communication About Breast Cancer-Related Internet Information and Its Effect on Patient Satisfaction and Anxiety; ODM derived from: https://clinicaltrials.gov/show/NCT00712569
Länk
https://clinicaltrials.gov/show/NCT00712569
Nyckelord
Versioner (1)
- 2017-10-16 2017-10-16 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
16 oktober 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00712569
Eligibility Breast Cancer NCT00712569
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00712569
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Inclusion criteria Patients
Item
subject inclusion criteria for patients
boolean
C1512693 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
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])
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])
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])
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])
C0679823 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Informed Consent
Item
provide inform consent
boolean
C0021430 (UMLS CUI [1])
Exclusion Criteria Patients
Item
exclusion criteria for patients
boolean
C0680251 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
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])
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])
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])
C0031831 (UMLS CUI [1,2])
None
Item
none
boolean
C0549184 (UMLS CUI [1])