ID

44777

Description

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

Lien

https://clinicaltrials.gov/show/NCT02485730

Mots-clés

  1. 30/08/2015 30/08/2015 -
  2. 18/11/2021 18/11/2021 -
Détendeur de droits

Barcelonabeta Brain Research Center, Pasqual Maragall Foundation

Téléchargé le

18 novembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :


Aucun commentaire

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Alzheimer's Disease NCT02485730

Eligibility Alzheimer's Disease NCT02485730

Inclusion Criteria
Description

Inclusion Criteria

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

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

Type de données

boolean

Alias
UMLS CUI [1,1]
C0002395
UMLS CUI [1,2]
C1517194
age: 45 to 64 years old.
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
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.
Description

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.

Type de données

boolean

Alias
UMLS CUI [1]
C0870312
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI [1]
C0680251
cognitive impairment: to be included the participant must show no signs of objective cognitive impairment.
Description

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

Type de données

boolean

Alias
UMLS CUI [1]
C1839000
any significant systemic illness or unstable medical condition which could lead to difficulty complying with the protocol.
Description

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

Type de données

boolean

Alias
UMLS CUI [1]
C0442893
UMLS CUI [2]
C0443343
illiteracy or functional illiteracy.
Description

illiteracy or functional illiteracy.

Type de données

boolean

Alias
UMLS CUI [1]
C0476584
any contraindication to any test or procedure.
Description

any contraindication to any test or procedure.

Type de données

boolean

Alias
UMLS CUI [1]
C1542040
family history of monogenic ad.
Description

family history of monogenic ad.

Type de données

boolean

Alias
UMLS CUI [1]
C1271045
not willing to undergo one or more of the tests and procedures described as mandatory in the protocol.
Description

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

Type de données

boolean

Alias
UMLS CUI [1]
C0558080

Similar models

Eligibility Alzheimer's Disease NCT02485730

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial