ID

39352

Description

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

Link

https://clinicaltrials.gov/show/NCT01875419

Keywords

Versions (2)
  1. 1/19/19 1/19/19 -
  2. 12/31/19 12/31/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

December 31, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Unipolar Major Depressive Disorder NCT01875419

English

Eligibility Unipolar Major Depressive Disorder NCT01875419

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

unipolar major depressive disorder

Data type

boolean

Alias
UMLS CUI [1,1]
C1269683
UMLS CUI [1,2]
C0443340
first depressive episode onset before 40 years old
Description

first depressive episode onset

Data type

boolean

Alias
UMLS CUI [1,1]
C0332189
UMLS CUI [1,2]
C0011581
UMLS CUI [2,1]
C1969363
UMLS CUI [2,2]
C0332152
right-handedness
Description

right-handedness

Data type

boolean

Alias
UMLS CUI [1]
C0344333
english as first language
Description

english as first language

Data type

boolean

Alias
UMLS CUI [1,1]
C0557073
UMLS CUI [1,2]
C0376245
intention to commence a course of cognitive behavioural therapy
Description

intention to commence a course of cognitive behavioural therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0009244
UMLS CUI [1,2]
C0162425
UMLS CUI [1,3]
C0679823
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

psychotropic medication

Data type

boolean

Alias
UMLS CUI [1,1]
C0033978
UMLS CUI [1,2]
C2347804
UMLS CUI [2,1]
C0033978
UMLS CUI [2,2]
C0332185
UMLS CUI [3,1]
C0003289
UMLS CUI [3,2]
C2347804
UMLS CUI [4,1]
C0003289
UMLS CUI [4,2]
C0332185
UMLS CUI [5,1]
C0016365
UMLS CUI [5,2]
C2347804
UMLS CUI [6,1]
C0016365
UMLS CUI [6,2]
C0332185
recent illicit drug use
Description

recent illicit drug use

Data type

boolean

Alias
UMLS CUI [1,1]
C0281875
UMLS CUI [1,2]
C0332185
prior mixed, manic, or psychotic symptoms or other psychiatric or neurological illness
Description

prior psychiatric or neurological illness

Data type

boolean

Alias
UMLS CUI [1]
C0871189
UMLS CUI [2]
C0746402
UMLS CUI [3,1]
C0871189
UMLS CUI [3,2]
C0746402
UMLS CUI [3,3]
C0205430
UMLS CUI [4]
C0004936
UMLS CUI [5]
C0027765
standard exclusion criteria for mri scanning: pregnancy, breast feeding, any immovable metal in the body, weight above 250 lbs, claustrophobia
Description

exclusion criteria for mri scanning

Data type

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0024485
UMLS CUI [2]
C0032961
UMLS CUI [3]
C0006147
UMLS CUI [4,1]
C2826620
UMLS CUI [4,2]
C0021102
UMLS CUI [5]
C0497406
UMLS CUI [6]
C0008909
tdcs safety criteria: skin disease or skin treatment that could potentially cause irritation with electrical stimulation
Description

tdcs safety criteria

Data type

boolean

Alias
UMLS CUI [1,1]
C3850024
UMLS CUI [1,2]
C0680251
UMLS CUI [2,1]
C0037274
UMLS CUI [2,2]
C0559546
UMLS CUI [2,3]
C0152030
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C0559546
UMLS CUI [3,3]
C0152030
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Similar models

Eligibility Unipolar Major Depressive Disorder NCT01875419

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
unipolar major depressive disorder
Item
patients suffering from unipolar major depressive disorder
boolean
C1269683 (UMLS CUI [1,1])
C0443340 (UMLS CUI [1,2])
first depressive episode onset
Item
first depressive episode onset before 40 years old
boolean
C0332189 (UMLS CUI [1,1])
C0011581 (UMLS CUI [1,2])
C1969363 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
right-handedness
Item
right-handedness
boolean
C0344333 (UMLS CUI [1])
english as first language
Item
english as first language
boolean
C0557073 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
intention to commence a course of cognitive behavioural therapy
Item
intention to commence a course of cognitive behavioural therapy
boolean
C0009244 (UMLS CUI [1,1])
C0162425 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
psychotropic medication
Item
antidepressant or other psychotropic medication at any time during the study or within previous 4 weeks (8 for fluoxetine)
boolean
C0033978 (UMLS CUI [1,1])
C2347804 (UMLS CUI [1,2])
C0033978 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
C0003289 (UMLS CUI [3,1])
C2347804 (UMLS CUI [3,2])
C0003289 (UMLS CUI [4,1])
C0332185 (UMLS CUI [4,2])
C0016365 (UMLS CUI [5,1])
C2347804 (UMLS CUI [5,2])
C0016365 (UMLS CUI [6,1])
C0332185 (UMLS CUI [6,2])
recent illicit drug use
Item
recent illicit drug use
boolean
C0281875 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
prior psychiatric or neurological illness
Item
prior mixed, manic, or psychotic symptoms or other psychiatric or neurological illness
boolean
C0871189 (UMLS CUI [1])
C0746402 (UMLS CUI [2])
C0871189 (UMLS CUI [3,1])
C0746402 (UMLS CUI [3,2])
C0205430 (UMLS CUI [3,3])
C0004936 (UMLS CUI [4])
C0027765 (UMLS CUI [5])
exclusion criteria for mri scanning
Item
standard exclusion criteria for mri scanning: pregnancy, breast feeding, any immovable metal in the body, weight above 250 lbs, claustrophobia
boolean
C0680251 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
C2826620 (UMLS CUI [4,1])
C0021102 (UMLS CUI [4,2])
C0497406 (UMLS CUI [5])
C0008909 (UMLS CUI [6])
tdcs safety criteria
Item
tdcs safety criteria: skin disease or skin treatment that could potentially cause irritation with electrical stimulation
boolean
C3850024 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
C0037274 (UMLS CUI [2,1])
C0559546 (UMLS CUI [2,2])
C0152030 (UMLS CUI [2,3])
C0087111 (UMLS CUI [3,1])
C0559546 (UMLS CUI [3,2])
C0152030 (UMLS CUI [3,3])
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