ID

34608

Description

Non-invasive Brain Stimulation and Cognitive Processing in Depression; ODM derived from: https://clinicaltrials.gov/show/NCT01875419

Lien

https://clinicaltrials.gov/show/NCT01875419

Mots-clés

  1. 19/01/2019 19/01/2019 -
  2. 31/12/2019 31/12/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

19 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Eligibility Unipolar Major Depressive Disorder NCT01875419

Eligibility Unipolar Major Depressive Disorder NCT01875419

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients suffering from unipolar major depressive disorder
Description

ID.1

Type de données

boolean

first depressive episode onset before 40 years old
Description

ID.2

Type de données

boolean

right-handedness
Description

ID.3

Type de données

boolean

english as first language
Description

ID.4

Type de données

boolean

intention to commence a course of cognitive behavioural therapy
Description

ID.5

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
antidepressant or other psychotropic medication at any time during the study or within previous 4 weeks (8 for fluoxetine)
Description

ID.6

Type de données

boolean

recent illicit drug use
Description

ID.7

Type de données

boolean

prior mixed, manic, or psychotic symptoms or other psychiatric or neurological illness
Description

ID.8

Type de données

boolean

standard exclusion criteria for mri scanning: pregnancy, breast feeding, any immovable metal in the body, weight above 250 lbs, claustrophobia
Description

ID.9

Type de données

boolean

tdcs safety criteria: skin disease or skin treatment that could potentially cause irritation with electrical stimulation
Description

ID.10

Type de données

boolean

Similar models

Eligibility Unipolar Major Depressive Disorder NCT01875419

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients suffering from unipolar major depressive disorder
boolean
ID.2
Item
first depressive episode onset before 40 years old
boolean
ID.3
Item
right-handedness
boolean
ID.4
Item
english as first language
boolean
ID.5
Item
intention to commence a course of cognitive behavioural therapy
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
antidepressant or other psychotropic medication at any time during the study or within previous 4 weeks (8 for fluoxetine)
boolean
ID.7
Item
recent illicit drug use
boolean
ID.8
Item
prior mixed, manic, or psychotic symptoms or other psychiatric or neurological illness
boolean
ID.9
Item
standard exclusion criteria for mri scanning: pregnancy, breast feeding, any immovable metal in the body, weight above 250 lbs, claustrophobia
boolean
ID.10
Item
tdcs safety criteria: skin disease or skin treatment that could potentially cause irritation with electrical stimulation
boolean

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