Information:
Fel:
ID
20206
Beskrivning
Trial of a Multilevel Intervention to Increase Colorectal Cancer Screening; ODM derived from: https://clinicaltrials.gov/show/NCT00836303
Länk
https://clinicaltrials.gov/show/NCT00836303
Nyckelord
Versioner (1)
- 2017-02-13 2017-02-13 -
Uppladdad den
13 februari 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT00836303
Eligibility Colorectal Cancer NCT00836303
- StudyEvent: Eligibility
Similar models
Eligibility Colorectal Cancer NCT00836303
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Adult | Latinos Immigrants
Item
adult latino immigrants
boolean
C0001675 (UMLS CUI [1])
C0086528 (UMLS CUI [2,1])
C0282163 (UMLS CUI [2,2])
C0086528 (UMLS CUI [2,1])
C0282163 (UMLS CUI [2,2])
Gender
Item
men and women
boolean
C0079399 (UMLS CUI [1])
Age
Item
50 years and older
boolean
C0001779 (UMLS CUI [1])
Clinic Primary Care Visit Quantity
Item
having had at least 2 previous visits to the primary care clinic in the past 2 years
boolean
C1552443 (UMLS CUI [1,1])
C1512346 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C1512346 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Colorectal Carcinoma | Family history of colorectal cancer
Item
personal or family history of colorectal cancer.
boolean
C0009402 (UMLS CUI [1])
C3266797 (UMLS CUI [2])
C3266797 (UMLS CUI [2])
Fecal occult blood test | Diagnostic flexible sigmoidoscopy | Barium enema | Colonoscopy
Item
had fecal occult blood testing (fobt) in the past year, or flexible sigmoidoscopy or barium enema in the past 5 years, or colonoscopy in the past 10 years.
boolean
C0201811 (UMLS CUI [1])
C3522028 (UMLS CUI [2])
C0203075 (UMLS CUI [3])
C0009378 (UMLS CUI [4])
C3522028 (UMLS CUI [2])
C0203075 (UMLS CUI [3])
C0009378 (UMLS CUI [4])
Lower Gastrointestinal Tract Symptoms | Lower gastrointestinal hemorrhage | Lower Gastrointestinal Tract Pain | Diarrhea | Constipation
Item
lower gastrointestinal symptoms, including bleeding, pain, diarrhea and/or constipation.
boolean
C0226875 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0024050 (UMLS CUI [2])
C0226875 (UMLS CUI [3,1])
C0030193 (UMLS CUI [3,2])
C0011991 (UMLS CUI [4])
C0009806 (UMLS CUI [5])
C1457887 (UMLS CUI [1,2])
C0024050 (UMLS CUI [2])
C0226875 (UMLS CUI [3,1])
C0030193 (UMLS CUI [3,2])
C0011991 (UMLS CUI [4])
C0009806 (UMLS CUI [5])
Illness Severe | Study Subject Participation Status Exclusion
Item
too ill to participate
boolean
C0221423 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
C0205082 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
Malignant Neoplasms | Skin carcinoma
Item
any cancer diagnosis other than non-melanoma skin cancer.
boolean
C0006826 (UMLS CUI [1])
C0699893 (UMLS CUI [2])
C0699893 (UMLS CUI [2])