ID

13194

Description

Dichotic Listening as a Predictor of Medication Response in Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00296725

Link

https://clinicaltrials.gov/show/NCT00296725

Keywords

  1. 1/23/16 1/23/16 -
Uploaded on

January 23, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Major Depression NCT00296725

Eligibility Major Depression NCT00296725

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
ages between 18-65
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
meets dsm-iv criteria for current major depression, dysthymia or depression nos
Description

major depression, dysthymia or depression nos

Data type

boolean

Alias
UMLS CUI [1]
C1269683
UMLS CUI [2]
C0013415
UMLS CUI [3]
C0011581
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known hearing impairment
Description

hearing impairment

Data type

boolean

Alias
UMLS CUI [1]
C1384666
active suicidal ideation (history of suicide attempts will be evaluated on a case by case basis)
Description

Suicidality

Data type

boolean

Alias
UMLS CUI [1]
C0438696
hamd > 20
Description

hamd

Data type

boolean

Alias
UMLS CUI [1]
C0451203
current (past six months) alcohol and/or drug abuse or dependence
Description

alcohol and/or drug abuse or dependence

Data type

boolean

Alias
UMLS CUI [1]
C0038586
medical condition likely to require intervention contraindicated with study medication (e.g., known arrhythmia likely to be exacerbated by imipramine)
Description

medical condition contraindicated with study medication

Data type

boolean

Alias
UMLS CUI [1]
C0009488
bipolar i
Description

bipolar i

Data type

boolean

Alias
UMLS CUI [1]
C0005586
UMLS CUI [2]
C0853193
psychosis
Description

psychosis

Data type

boolean

Alias
UMLS CUI [1]
C0033975
if currently taking antidepressants or mood stabilizers, cannot be off psychotropic medication for 7 weeks (10 weeks for prozac) or felt to require other psychiatric medication (other than occasional sleep or anxiety medication)
Description

psychatric medication

Data type

boolean

Alias
UMLS CUI [1]
C0003289
UMLS CUI [2]
C4020582
UMLS CUI [3]
C0748066
premenopausal women not using known effective birth control
Description

birth control

Data type

boolean

Alias
UMLS CUI [1]
C0700589
not currently depressed (whether considered due to current treatment or not)
Description

not currently depressed

Data type

boolean

Alias
UMLS CUI [1]
C0344315
UMLS CUI [2]
C0011570
nonresponse to adequate trial of both study medications (i.e., > 4weeks on > escitalopram 30 mg/d, and imipramine 200 mg/d); patients having an inadequate response to one study medication could be enrolled and receive the other; patients having responded to an adequate trial of either study medication would be offered a retrial; also excluded will be subjects having non responded to an adequate trial with citalopram (i.e., > 4 weeks on > citalopram 60 mg/d)
Description

response to treatment, escitalporam, imipramine

Data type

boolean

Alias
UMLS CUI [1]
C0521982
UMLS CUI [2]
C1099456
UMLS CUI [3]
C0020934
left-handed
Description

left handed

Data type

boolean

Alias
UMLS CUI [1]
C0234418

Similar models

Eligibility Major Depression NCT00296725

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
ages between 18-65
boolean
C0001779 (UMLS CUI [1])
major depression, dysthymia or depression nos
Item
meets dsm-iv criteria for current major depression, dysthymia or depression nos
boolean
C1269683 (UMLS CUI [1])
C0013415 (UMLS CUI [2])
C0011581 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
hearing impairment
Item
known hearing impairment
boolean
C1384666 (UMLS CUI [1])
Suicidality
Item
active suicidal ideation (history of suicide attempts will be evaluated on a case by case basis)
boolean
C0438696 (UMLS CUI [1])
hamd
Item
hamd > 20
boolean
C0451203 (UMLS CUI [1])
alcohol and/or drug abuse or dependence
Item
current (past six months) alcohol and/or drug abuse or dependence
boolean
C0038586 (UMLS CUI [1])
medical condition contraindicated with study medication
Item
medical condition likely to require intervention contraindicated with study medication (e.g., known arrhythmia likely to be exacerbated by imipramine)
boolean
C0009488 (UMLS CUI [1])
bipolar i
Item
bipolar i
boolean
C0005586 (UMLS CUI [1])
C0853193 (UMLS CUI [2])
psychosis
Item
psychosis
boolean
C0033975 (UMLS CUI [1])
psychatric medication
Item
if currently taking antidepressants or mood stabilizers, cannot be off psychotropic medication for 7 weeks (10 weeks for prozac) or felt to require other psychiatric medication (other than occasional sleep or anxiety medication)
boolean
C0003289 (UMLS CUI [1])
C4020582 (UMLS CUI [2])
C0748066 (UMLS CUI [3])
birth control
Item
premenopausal women not using known effective birth control
boolean
C0700589 (UMLS CUI [1])
not currently depressed
Item
not currently depressed (whether considered due to current treatment or not)
boolean
C0344315 (UMLS CUI [1])
C0011570 (UMLS CUI [2])
response to treatment, escitalporam, imipramine
Item
nonresponse to adequate trial of both study medications (i.e., > 4weeks on > escitalopram 30 mg/d, and imipramine 200 mg/d); patients having an inadequate response to one study medication could be enrolled and receive the other; patients having responded to an adequate trial of either study medication would be offered a retrial; also excluded will be subjects having non responded to an adequate trial with citalopram (i.e., > 4 weeks on > citalopram 60 mg/d)
boolean
C0521982 (UMLS CUI [1])
C1099456 (UMLS CUI [2])
C0020934 (UMLS CUI [3])
left handed
Item
left-handed
boolean
C0234418 (UMLS CUI [1])

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