Informatie:
Fout:
ID
43745
Beschrijving
A Mammography FastTrack Program in Increasing the Number of Women Undergoing Breast Cancer Screening; ODM derived from: https://clinicaltrials.gov/show/NCT00462891
Link
https://clinicaltrials.gov/show/NCT00462891
Trefwoorden
Versies (2)
- 05-10-17 05-10-17 -
- 20-09-21 20-09-21 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
20 september 2021
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00462891
Eligibility Breast Cancer NCT00462891
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00462891
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Outpatient | Participating Clinical Study Organization Practice-based Research Network
Item
any outpatient at a participating massachusetts general primary care practice-based research network (mgpc-pbrn) practice within the past 3 years
boolean
C0029921 (UMLS CUI [1])
C2347449 (UMLS CUI [2,1])
C1709626 (UMLS CUI [2,2])
C2347449 (UMLS CUI [2,1])
C1709626 (UMLS CUI [2,2])
Primary care provider Other | Patient Excluded
Item
no patient who the massachusetts general hospital system lists as having a primary care provider who is not in one of the mgpc-pbrn networks (linking patients with a provider or practice)
boolean
C2735026 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0030705 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
C0205394 (UMLS CUI [1,2])
C0030705 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
Exclusion Criteria | Lacking Primary care provider Specific
Item
no patient who is not linked to specific provider or practice (randomized portion of study)
boolean
C0680251 (UMLS CUI [1])
C0332268 (UMLS CUI [2,1])
C2735026 (UMLS CUI [2,2])
C0205369 (UMLS CUI [2,3])
C0332268 (UMLS CUI [2,1])
C2735026 (UMLS CUI [2,2])
C0205369 (UMLS CUI [2,3])
Requirement Billing Data | Requirement Scheduling Data | Requirement Clinical Data Electronic
Item
billing, scheduling, and clinical electronic data sources required
boolean
C1514873 (UMLS CUI [1,1])
C2987582 (UMLS CUI [1,2])
C1511726 (UMLS CUI [1,3])
C1514873 (UMLS CUI [2,1])
C1446911 (UMLS CUI [2,2])
C1511726 (UMLS CUI [2,3])
C1514873 (UMLS CUI [3,1])
C1516606 (UMLS CUI [3,2])
C0013850 (UMLS CUI [3,3])
C2987582 (UMLS CUI [1,2])
C1511726 (UMLS CUI [1,3])
C1514873 (UMLS CUI [2,1])
C1446911 (UMLS CUI [2,2])
C1511726 (UMLS CUI [2,3])
C1514873 (UMLS CUI [3,1])
C1516606 (UMLS CUI [3,2])
C0013850 (UMLS CUI [3,3])
Mammography Absent
Item
no mammogram within the past 2 years (randomized portion of study)
boolean
C0024671 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Age
Item
age 42 to 69 years (randomized portion of study)
boolean
C0001779 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C3829127 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Bilateral mastectomy Absent
Item
no prior bilateral mastectomy (randomized portion of study)
boolean
C0191877 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])