ID

44777

Descrizione

Early Identification of Markers in Alzheimer's Families / ALFA; ODM derived from: https://clinicaltrials.gov/show/NCT02485730

collegamento

https://clinicaltrials.gov/show/NCT02485730

Keywords

  1. 30/08/15 30/08/15 -
  2. 18/11/21 18/11/21 -
Titolare del copyright

Barcelonabeta Brain Research Center, Pasqual Maragall Foundation

Caricato su

18 novembre 2021

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Alzheimer's Disease NCT02485730

Eligibility Alzheimer's Disease NCT02485730

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI [1]
C1512693 (Inclusion)
adult children of ad patient: first-degree descendant of an ad patient (following diagnosis as define in protocol).
Descrizione

adult children of ad patient: first-degree descendant of an ad patient (following diagnosis as define in protocol).

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0002395 (Alzheimer's Disease)
SNOMED
26929004
UMLS CUI [1,2]
C1517194 (First Degree Relative)
age: 45 to 64 years old.
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779 (Age)
SNOMED
424144002
LOINC
LP28815-6
long-term commitment to the study: baseline and follow-up visits. potential participants have to agree to undergo at baseline all tests, mri and lumbar puncture (lp), since they are considered to be mandatory in this study.
Descrizione

long-term commitment to the study: baseline and follow-up visits. potential participants have to agree to undergo at baseline all tests, mri and lumbar puncture (lp), since they are considered to be mandatory in this study.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0870312 (commitment)
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI [1]
C0680251 (Exclusion Criteria)
cognitive impairment: to be included the participant must show no signs of objective cognitive impairment.
Descrizione

cognitive impairment: to be included the participant must show no signs of objective cognitive impairment.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1839000 (Cognitive impairment (CVS+))
any significant systemic illness or unstable medical condition which could lead to difficulty complying with the protocol.
Descrizione

any significant systemic illness or unstable medical condition which could lead to difficulty complying with the protocol.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0442893 (Systemic disease)
SNOMED
56019007
UMLS CUI [2]
C0443343 (Unstable status)
SNOMED
263922001
LOINC
LP28572-3
illiteracy or functional illiteracy.
Descrizione

illiteracy or functional illiteracy.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0476584 (Illiteracy and low-level literacy)
any contraindication to any test or procedure.
Descrizione

any contraindication to any test or procedure.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1542040 (Contraindication to procedure (& [medical] or [to surgery]))
family history of monogenic ad.
Descrizione

family history of monogenic ad.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1271045 (FH: Alzheimer's disease)
SNOMED
394877006
not willing to undergo one or more of the tests and procedures described as mandatory in the protocol.
Descrizione

not willing to undergo one or more of the tests and procedures described as mandatory in the protocol.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0558080 (Unwilling)
SNOMED
225465005

Similar models

Eligibility Alzheimer's Disease NCT02485730

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI [1])
diagnosis; protocol; degree; first
Item
adult children of ad patient: first-degree descendant of an ad patient (following diagnosis as define in protocol).
boolean
C0002395 (UMLS CUI [1,1])
C1517194 (UMLS CUI [1,2])
age
Item
age: 45 to 64 years old.
boolean
C0001779 (UMLS CUI [1])
follow-up visit; lumbar puncture; participants; baseline; agree; study; mri; all
Item
long-term commitment to the study: baseline and follow-up visits. potential participants have to agree to undergo at baseline all tests, mri and lumbar puncture (lp), since they are considered to be mandatory in this study.
boolean
C0870312 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI [1])
impairment; objective; signs
Item
cognitive impairment: to be included the participant must show no signs of objective cognitive impairment.
boolean
C1839000 (UMLS CUI [1])
medical condition; protocol; systemic
Item
any significant systemic illness or unstable medical condition which could lead to difficulty complying with the protocol.
boolean
C0442893 (UMLS CUI [1])
C0443343 (UMLS CUI [2])
no code found
Item
illiteracy or functional illiteracy.
boolean
C0476584 (UMLS CUI [1])
procedure; test
Item
any contraindication to any test or procedure.
boolean
C1542040 (UMLS CUI [1])
family history
Item
family history of monogenic ad.
boolean
C1271045 (UMLS CUI [1])
procedure(s); procedures; protocol; one
Item
not willing to undergo one or more of the tests and procedures described as mandatory in the protocol.
boolean
C0558080 (UMLS CUI [1])

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