Age
Item
age 18-65
boolean
C0001779 (UMLS CUI [1])
Schizophrenia
Item
a diagnosis of schizophrenia (dsm-ivtr)
boolean
C0036341 (UMLS CUI [1])
Antipsychotic Agent Dose unchanged
Item
antipsychotic dose unchanged for at least 2 weeks prior to study
boolean
C0040615 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0442739 (UMLS CUI [1,3])
Rating scale Schizophrenia Symptoms Negative | Affective blunting | Alogia | Avolition
Item
sans score>= 3 on at least one of the global measures of affective blunting, alogia or avolition.
boolean
C0681889 (UMLS CUI [1,1])
C0036341 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C1513916 (UMLS CUI [1,4])
C0860608 (UMLS CUI [2])
C0003537 (UMLS CUI [3])
C3495892 (UMLS CUI [4])
Knowledge Hebrew language
Item
knowledge of hebrew
boolean
C0376554 (UMLS CUI [1,1])
C0018863 (UMLS CUI [1,2])
Dementia | Nervous system disorder Serious
Item
dementia or other serious neurological disorders
boolean
C0497327 (UMLS CUI [1])
C0027765 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
Substance Use Disorders
Item
history of alcohol or drug use
boolean
C0038586 (UMLS CUI [1])
Patient Has Legal Guardian
Item
patients with a legal guardian
boolean
C0030705 (UMLS CUI [1,1])
C3539897 (UMLS CUI [1,2])
C0023226 (UMLS CUI [1,3])
Involuntary Hospitalization
Item
patients involuntarily hospitalized by order of the district psychiatrist
boolean
C0745037 (UMLS CUI [1])
Antidepressive Agents
Item
use of antidepressants within 1 month of the study
boolean
C0003289 (UMLS CUI [1])
Kidney Diseases | Liver diseases
Item
renal or hepatic disorder
boolean
C0022658 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
Upper gastrointestinal hemorrhage
Item
patients with upper gi bleeds
boolean
C0041909 (UMLS CUI [1])
Inappropriate ADH Syndrome
Item
patients with siadh syndrome
boolean
C0021141 (UMLS CUI [1])
Pregnancy
Item
pregnant woman
boolean
C0032961 (UMLS CUI [1])
Criteria Cessation Clinical Trial
Item
criteria for the cessation of the study after initial commencement:
boolean
C0243161 (UMLS CUI [1,1])
C1880019 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Adverse events Severe | Adverse events Gastrointestinal Severe | Adverse events Cardiovascular Severe | Adverse events Neurologic Severe | Adverse events Hematologic Severe | Adverse events Urologic Severe
Item
severe adverse events (including but not only gi, cardiovascular, neurologic, hematologic or urologic severe adverse events)
boolean
C0877248 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C0521362 (UMLS CUI [2,2])
C0205082 (UMLS CUI [2,3])
C0877248 (UMLS CUI [3,1])
C3887460 (UMLS CUI [3,2])
C0205082 (UMLS CUI [3,3])
C0877248 (UMLS CUI [4,1])
C0205494 (UMLS CUI [4,2])
C0205082 (UMLS CUI [4,3])
C0877248 (UMLS CUI [5,1])
C0205488 (UMLS CUI [5,2])
C0205082 (UMLS CUI [5,3])
C0877248 (UMLS CUI [6,1])
C0042077 (UMLS CUI [6,2])
C0205082 (UMLS CUI [6,3])
Emergency Suicidality
Item
emergent suicidality
boolean
C2745965 (UMLS CUI [1,1])
C3166387 (UMLS CUI [1,2])
Emergency Symptoms Hypomania | Emergency Manic symptom
Item
emergence of hypomanic or manic symptoms
boolean
C2745965 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0241934 (UMLS CUI [1,3])
C2745965 (UMLS CUI [2,1])
C0746402 (UMLS CUI [2,2])
Cessation Requested by patient
Item
if the subject requests to stop
boolean
C1880019 (UMLS CUI [1,1])
C0332153 (UMLS CUI [1,2])