Informações:
Falhas:
ID
35669
Descrição
CBT Versus Selective Serotonin Reuptake Inhibitor For Treatment Of Depression In Temporal Lobe Epilepsy Patients; ODM derived from: https://clinicaltrials.gov/show/NCT02262156
Link
https://clinicaltrials.gov/show/NCT02262156
Palavras-chave
Versões (1)
- 15/03/2019 15/03/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
15 de março de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Depression NCT02262156
Eligibility Depression NCT02262156
- StudyEvent: Eligibility
Similar models
Eligibility Depression NCT02262156
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0311392 (UMLS CUI [2,1])
C0011581 (UMLS CUI [2,2])
High suicide risk | Hospitalization Required
Item
patients with high risk of suicide who required hospitalization
boolean
C1271074 (UMLS CUI [1])
C1708385 (UMLS CUI [2])
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])
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])
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])