ID

20206

Descripción

Trial of a Multilevel Intervention to Increase Colorectal Cancer Screening; ODM derived from: https://clinicaltrials.gov/show/NCT00836303

Link

https://clinicaltrials.gov/show/NCT00836303

Palabras clave

Versiones (1)
  1. 13/2/17 13/2/17 -
Subido en

13 de febrero de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT00836303

Inglés

Eligibility Colorectal Cancer NCT00836303

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult latino immigrants
Descripción

Adult | Latinos Immigrants

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2,1]
C0086528
UMLS CUI [2,2]
C0282163
men and women
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
50 years and older
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
having had at least 2 previous visits to the primary care clinic in the past 2 years
Descripción

Clinic Primary Care Visit Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1552443
UMLS CUI [1,2]
C1512346
UMLS CUI [1,3]
C1265611
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
personal or family history of colorectal cancer.
Descripción

Colorectal Carcinoma | Family history of colorectal cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009402
UMLS CUI [2]
C3266797
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.
Descripción

Fecal occult blood test | Diagnostic flexible sigmoidoscopy | Barium enema | Colonoscopy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201811
UMLS CUI [2]
C3522028
UMLS CUI [3]
C0203075
UMLS CUI [4]
C0009378
lower gastrointestinal symptoms, including bleeding, pain, diarrhea and/or constipation.
Descripción

Lower Gastrointestinal Tract Symptoms | Lower gastrointestinal hemorrhage | Lower Gastrointestinal Tract Pain | Diarrhea | Constipation

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0226875
UMLS CUI [1,2]
C1457887
UMLS CUI [2]
C0024050
UMLS CUI [3,1]
C0226875
UMLS CUI [3,2]
C0030193
UMLS CUI [4]
C0011991
UMLS CUI [5]
C0009806
too ill to participate
Descripción

Illness Severe | Study Subject Participation Status Exclusion

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C2348568
UMLS CUI [2,2]
C2828389
any cancer diagnosis other than non-melanoma skin cancer.
Descripción

Malignant Neoplasms | Skin carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0699893
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Similar models

Eligibility Colorectal Cancer NCT00836303

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Latinos Immigrants
Item
adult latino immigrants
boolean
C0001675 (UMLS CUI [1])
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])
Item Group
C0680251 (UMLS CUI)
Colorectal Carcinoma | Family history of colorectal cancer
Item
personal or family history of colorectal cancer.
boolean
C0009402 (UMLS CUI [1])
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])
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])
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])
Malignant Neoplasms | Skin carcinoma
Item
any cancer diagnosis other than non-melanoma skin cancer.
boolean
C0006826 (UMLS CUI [1])
C0699893 (UMLS CUI [2])
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