Information:
Fel:
ID
20194
Beskrivning
Bilingual Breast Cancer Educational Intervention for Hispanic Women With Stage I, Stage II, or Stage III Breast Cancer and Their Families or Caregivers; ODM derived from: https://clinicaltrials.gov/show/NCT01043003
Länk
https://clinicaltrials.gov/show/NCT01043003
Nyckelord
Versioner (1)
- 2017-02-11 2017-02-11 -
Uppladdad den
11 februari 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01043003
Eligibility Breast Cancer NCT01043003
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01043003
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Breast cancer stage
Item
histologically confirmed diagnosis of stage 0 (dcis), i, ii, or iii breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0027646 (UMLS CUI [1,2])
C0027646 (UMLS CUI [1,2])
Recurrent, metastatic, or second primary cancer
Item
no evidence of recurrent, metastatic, or second primary cancer
boolean
C0549379 (UMLS CUI [1])
C0027627 (UMLS CUI [2])
C0751623 (UMLS CUI [3])
C0027627 (UMLS CUI [2])
C0751623 (UMLS CUI [3])
Primary treatment
Item
completing primary treatment with surgery, radiation therapy (if indicated), and/or adjuvant chemotherapy (if indicated)
boolean
C1708063 (UMLS CUI [1])
Hormonal therapy
Item
subjects may be on hormonal therapy after treatment for initial breast cancer
boolean
C0279025 (UMLS CUI [1])
Hispanics
Item
self-identification as hispanic/latino
boolean
C0086409 (UMLS CUI [1])
Language
Item
able to read and understand english or spanish to participate in the patient teaching
boolean
C1145677 (UMLS CUI [1])
Study status
Item
able and willing to participate in the study
boolean
C2348568 (UMLS CUI [1])
Caregiver
Item
the caregiver selection criteria is: self-identification as the primary caregiver; age 18 years or over; self-identification as hispanic/latino; able to read and speak english or spanish; able and willing to participate in the study
boolean
C0085537 (UMLS CUI [1])
Exclusion
Item
exclusion
boolean
C2828389 (UMLS CUI [1])
Active treatment
Item
patients will be excluded if they are actively receiving treatment with surgery, radiation therapy, or chemotherapy; patients may be receiving adjuvant hormonal therapy such as tamoxifen during the course of the study since it is recommended for five years after primary and adjuvant therapy
boolean
C0087111 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,2])
Recurrence, metastasis, or a second primary cancer
Item
patients who have recurrence, metastasis, or a second primary cancer will not be recruited for the study; if however, they develop recurrence, metastasis, or a second primary cancer during the time of the study participation, the subjects will remain in the study
boolean
C0549379 (UMLS CUI [1])
C0027627 (UMLS CUI [2])
C0751623 (UMLS CUI [3])
C0027627 (UMLS CUI [2])
C0751623 (UMLS CUI [3])
Support groups
Item
patients will not be recruited directly from support groups because of potential bias inherent in sample attending support groups; however, some patients may be participating in support groups or other forms of counseling
boolean
C0036606 (UMLS CUI [1])