ID

27769

Descripción

Getting Biased Treatment Study: How Psychotherapy and Antidepressants Change Brain Activity in Chronic Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00596986

Link

https://clinicaltrials.gov/show/NCT00596986

Palabras clave

Versiones (1)
  1. 28/11/17 28/11/17 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

28 de noviembre de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Chronic Depression NCT00596986

Inglés

Eligibility Chronic Depression NCT00596986

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
chronic depression (double depression, chronic mde, mde with incomplete remission)
Descripción

Chronic depression | Depressive disorder Double | Chronic major depressive disorder, single episode | Single major depressive episode Partial remission

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0581391
UMLS CUI [2,1]
C0011581
UMLS CUI [2,2]
C0205173
UMLS CUI [3]
C0520666
UMLS CUI [4,1]
C0024517
UMLS CUI [4,2]
C1521726
hamd-24>20
Descripción

Hamilton rating scale for depression

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0451203
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
concurrent psychotherapy or psychopharmacotherapy
Descripción

Psychotherapy | Psychopharmacological therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0033968
UMLS CUI [2]
C0679629
previous non-response to duloxetine
Descripción

Duloxetine Unresponsive to Treatment

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0245561
UMLS CUI [1,2]
C0205269
non-response to three antidepressants of two different groups given at adequate doses or non-response to two empirically tested forms of psychotherapy in the current depressive episode
Descripción

Antidepressive Agents Unresponsive to Treatment | Antidepressive Agents Quantity Groups Different | Antidepressive Agents Dose Adequate | Psychotherapy Quantity Unresponsive to Treatment | Depressive episode Unresponsive to Treatment

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003289
UMLS CUI [1,2]
C0205269
UMLS CUI [2,1]
C0003289
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0441833
UMLS CUI [2,4]
C1705242
UMLS CUI [3,1]
C0003289
UMLS CUI [3,2]
C0178602
UMLS CUI [3,3]
C0205411
UMLS CUI [4,1]
C0033968
UMLS CUI [4,2]
C1265611
UMLS CUI [4,3]
C0205269
UMLS CUI [5,1]
C0349217
UMLS CUI [5,2]
C0205269
serious psychiatric comorbidity
Descripción

Comorbidity Psychiatric Serious

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205487
UMLS CUI [1,3]
C0205404
serious neurologic comorbidity
Descripción

Comorbidity Neurologic Serious

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205494
UMLS CUI [1,3]
C0205404
contraindications to duloxetine
Descripción

Medical contraindication Duloxetine

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0245561
contraindications to fmri
Descripción

Medical contraindication fMRI

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0376335
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Similar models

Eligibility Chronic Depression NCT00596986

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Chronic depression | Depressive disorder Double | Chronic major depressive disorder, single episode | Single major depressive episode Partial remission
Item
chronic depression (double depression, chronic mde, mde with incomplete remission)
boolean
C0581391 (UMLS CUI [1])
C0011581 (UMLS CUI [2,1])
C0205173 (UMLS CUI [2,2])
C0520666 (UMLS CUI [3])
C0024517 (UMLS CUI [4,1])
C1521726 (UMLS CUI [4,2])
Hamilton rating scale for depression
Item
hamd-24>20
boolean
C0451203 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Psychotherapy | Psychopharmacological therapy
Item
concurrent psychotherapy or psychopharmacotherapy
boolean
C0033968 (UMLS CUI [1])
C0679629 (UMLS CUI [2])
Duloxetine Unresponsive to Treatment
Item
previous non-response to duloxetine
boolean
C0245561 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
Antidepressive Agents Unresponsive to Treatment | Antidepressive Agents Quantity Groups Different | Antidepressive Agents Dose Adequate | Psychotherapy Quantity Unresponsive to Treatment | Depressive episode Unresponsive to Treatment
Item
non-response to three antidepressants of two different groups given at adequate doses or non-response to two empirically tested forms of psychotherapy in the current depressive episode
boolean
C0003289 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
C0003289 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0441833 (UMLS CUI [2,3])
C1705242 (UMLS CUI [2,4])
C0003289 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0205411 (UMLS CUI [3,3])
C0033968 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
C0205269 (UMLS CUI [4,3])
C0349217 (UMLS CUI [5,1])
C0205269 (UMLS CUI [5,2])
Comorbidity Psychiatric Serious
Item
serious psychiatric comorbidity
boolean
C0009488 (UMLS CUI [1,1])
C0205487 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,3])
Comorbidity Neurologic Serious
Item
serious neurologic comorbidity
boolean
C0009488 (UMLS CUI [1,1])
C0205494 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,3])
Medical contraindication Duloxetine
Item
contraindications to duloxetine
boolean
C1301624 (UMLS CUI [1,1])
C0245561 (UMLS CUI [1,2])
Medical contraindication fMRI
Item
contraindications to fmri
boolean
C1301624 (UMLS CUI [1,1])
C0376335 (UMLS CUI [1,2])
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