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Eligibility Criteria

6 Formulaires  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, consent group, and affection status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    3. Subject ID, sample ID, and sample use of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    4. Subject ID, sample ID, sample source, sample source ID, and sample use of samples obtained from subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    5. Subject ID, country of birth, recruitment site, education, sex, visit, study type, affection status of participants [case or control], family history of Alzheimer disease, participant history of diabetes, head injury, heart disease, hypertension, stoke, age at onset, age at examination, age at last examination, allele value of Apolipoprotein E, height and weight, systolic and diastolic blood pressure, color traits, daily living scale, dementia rating scale, score on recognition test, Mattis Dementia Rating Scale, Boston Naming Test, abstract reasoning from WAIS, and smoking status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    6. Sample ID, body site where sample was collected, analyte type, histological type, and tumor status of samples obtained from subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Cases meet NINCDS/ADRDA clinical criteria for Alzheimer's disease.
Description

Elig.phs000496.v1.p1.1

Type de données

boolean

Alias
UMLS CUI [1,1]
C3274647
UMLS CUI [1,2]
C1516637
UMLS CUI [1,3]
C2828081
Cases are familial, with a family history of dementia/Alzheimer's disease and sporadic, without a family history of dementia/Alzheimer's disease.
Description

Elig.phs000496.v1.p1.2

Type de données

boolean

Alias
UMLS CUI [2,1]
C3274647
UMLS CUI [2,2]
C0241888
UMLS CUI [2,3]
C2315857
UMLS CUI [2,4]
C1271045
UMLS CUI [3,1]
C3274647
UMLS CUI [3,2]
C0205422
UMLS CUI [3,3]
C2315857
UMLS CUI [3,4]
C1271045
UMLS CUI [3,5]
C0332288
Controls defined by the absence of dementia based on neurological exam and neuropsychological assessments.
Description

Elig.phs000496.v1.p1.3

Type de données

boolean

Alias
UMLS CUI [1,1]
C3274648
UMLS CUI [1,2]
C5239603
UMLS CUI [1,3]
C1838634
UMLS CUI [1,4]
C0027853
UMLS CUI [1,5]
C0027902
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Similar models

Eligibility Criteria

6 Formulaires
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. Subject ID, consent group, and affection status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    3. Subject ID, sample ID, and sample use of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    4. Subject ID, sample ID, sample source, sample source ID, and sample use of samples obtained from subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    5. Subject ID, country of birth, recruitment site, education, sex, visit, study type, affection status of participants [case or control], family history of Alzheimer disease, participant history of diabetes, head injury, heart disease, hypertension, stoke, age at onset, age at examination, age at last examination, allele value of Apolipoprotein E, height and weight, systolic and diastolic blood pressure, color traits, daily living scale, dementia rating scale, score on recognition test, Mattis Dementia Rating Scale, Boston Naming Test, abstract reasoning from WAIS, and smoking status of subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
    6. Sample ID, body site where sample was collected, analyte type, histological type, and tumor status of samples obtained from subjects with or without Alzheimer disease and involved in the "Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease" project.
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000496.v1.p1.1
Item
Cases meet NINCDS/ADRDA clinical criteria for Alzheimer's disease.
boolean
C3274647 (UMLS CUI [1,1])
C1516637 (UMLS CUI [1,2])
C2828081 (UMLS CUI [1,3])
Elig.phs000496.v1.p1.2
Item
Cases are familial, with a family history of dementia/Alzheimer's disease and sporadic, without a family history of dementia/Alzheimer's disease.
boolean
C3274647 (UMLS CUI [2,1])
C0241888 (UMLS CUI [2,2])
C2315857 (UMLS CUI [2,3])
C1271045 (UMLS CUI [2,4])
C3274647 (UMLS CUI [3,1])
C0205422 (UMLS CUI [3,2])
C2315857 (UMLS CUI [3,3])
C1271045 (UMLS CUI [3,4])
C0332288 (UMLS CUI [3,5])
Elig.phs000496.v1.p1.3
Item
Controls defined by the absence of dementia based on neurological exam and neuropsychological assessments.
boolean
C3274648 (UMLS CUI [1,1])
C5239603 (UMLS CUI [1,2])
C1838634 (UMLS CUI [1,3])
C0027853 (UMLS CUI [1,4])
C0027902 (UMLS CUI [1,5])
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