Eligibility Depression NCT02262156

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT02262156
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
with major depressive disorder according to criteria from the fourth edition of the diagnostic and statistical manual of mental disorders (dsm-iv)
Descrizione

Major Depressive Disorder

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1269683
diagnosed with tle according to the criteria of the international league against epilepsy
Descrizione

Epilepsy, Temporal Lobe

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0014556
literates had sign an informed consent
Descrizione

Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
patients on antidepressant treatments will be allowed to participate only if they had been at stable doses for more than 8 weeks and still show signs of significant depression
Descrizione

Antidepressant therapy Dose Stable | Signs Depressive disorder

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1096649
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
UMLS CUI [2,1]
C0311392
UMLS CUI [2,2]
C0011581
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with high risk of suicide who required hospitalization
Descrizione

High suicide risk | Hospitalization Required

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1271074
UMLS CUI [2]
C1708385
patients who abused or are dependent on drugs
Descrizione

Drug abuse | Drug Dependence

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0013146
UMLS CUI [2]
C1510472
those with a history of head trauma six months prior to the interview
Descrizione

Craniocerebral Trauma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0018674
patients who have any condition that would prevent them from understanding the study or the psychotherapeutic process, such as mental retardation, psychosis, delirium, dementia, etc
Descrizione

Condition Preventing Comprehension Study Protocol | Condition Preventing Comprehension Psychotherapeutic Process | Mental Retardation | Psychotic Disorders | Delirium | Dementia

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C1292733
UMLS CUI [1,3]
C0162340
UMLS CUI [1,4]
C2348563
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C1292733
UMLS CUI [2,3]
C0162340
UMLS CUI [2,4]
C0039792
UMLS CUI [3]
C0025362
UMLS CUI [4]
C0033975
UMLS CUI [5]
C0011206
UMLS CUI [6]
C0497327
patients who have previously received cbt
Descrizione

Cognitive Therapy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009244
patients who have started, an antidepressant drug the last 8 weeks
Descrizione

Antidepressive Agents

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0003289

Similar models

Eligibility Depression NCT02262156

  1. StudyEvent: Eligibility
    1. Eligibility Depression NCT02262156
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Major Depressive Disorder
Item
with major depressive disorder according to criteria from the fourth edition of the diagnostic and statistical manual of mental disorders (dsm-iv)
boolean
C1269683 (UMLS CUI [1])
Epilepsy, Temporal Lobe
Item
diagnosed with tle according to the criteria of the international league against epilepsy
boolean
C0014556 (UMLS CUI [1])
Informed Consent
Item
literates had sign an informed consent
boolean
C0021430 (UMLS CUI [1])
Antidepressant therapy Dose Stable | Signs Depressive disorder
Item
patients on antidepressant treatments will be allowed to participate only if they had been at stable doses for more than 8 weeks and still show signs of significant depression
boolean
C1096649 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0311392 (UMLS CUI [2,1])
C0011581 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
High suicide risk | Hospitalization Required
Item
patients with high risk of suicide who required hospitalization
boolean
C1271074 (UMLS CUI [1])
C1708385 (UMLS CUI [2])
Drug abuse | Drug Dependence
Item
patients who abused or are dependent on drugs
boolean
C0013146 (UMLS CUI [1])
C1510472 (UMLS CUI [2])
Craniocerebral Trauma
Item
those with a history of head trauma six months prior to the interview
boolean
C0018674 (UMLS CUI [1])
Condition Preventing Comprehension Study Protocol | Condition Preventing Comprehension Psychotherapeutic Process | Mental Retardation | Psychotic Disorders | Delirium | Dementia
Item
patients who have any condition that would prevent them from understanding the study or the psychotherapeutic process, such as mental retardation, psychosis, delirium, dementia, etc
boolean
C0348080 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C0162340 (UMLS CUI [1,3])
C2348563 (UMLS CUI [1,4])
C0348080 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,3])
C0039792 (UMLS CUI [2,4])
C0025362 (UMLS CUI [3])
C0033975 (UMLS CUI [4])
C0011206 (UMLS CUI [5])
C0497327 (UMLS CUI [6])
Cognitive Therapy
Item
patients who have previously received cbt
boolean
C0009244 (UMLS CUI [1])
Antidepressive Agents
Item
patients who have started, an antidepressant drug the last 8 weeks
boolean
C0003289 (UMLS CUI [1])