Informatie:
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ID
27769
Beschrijving
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
Trefwoorden
Versies (1)
- 28-11-17 28-11-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
28 november 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Chronic Depression NCT00596986
Eligibility Chronic Depression NCT00596986
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Depression NCT00596986
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
Psychotherapy | Psychopharmacological therapy
Item
concurrent psychotherapy or psychopharmacotherapy
boolean
C0033968 (UMLS CUI [1])
C0679629 (UMLS CUI [2])
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])
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])
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])
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])
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])
C0245561 (UMLS CUI [1,2])
Medical contraindication fMRI
Item
contraindications to fmri
boolean
C1301624 (UMLS CUI [1,1])
C0376335 (UMLS CUI [1,2])
C0376335 (UMLS CUI [1,2])