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Eligibility

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
Patient signed the written informed consent
Description

Informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Patient is an adult man or woman (aged 18-50 years)
Description

Age and gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
Patient with diagnosed schizophrenia or schizoaffective disorder (DSM IV)
Description

Diagnosis

Data type

boolean

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C0036341
UMLS CUI [1,3]
C0220952
UMLS CUI [2,1]
C0011900
UMLS CUI [2,2]
C0036337
UMLS CUI [2,3]
C0220952
Patient is less than 5 years (since onset of psychosis) ill.
Description

Illness duration

Data type

boolean

Alias
UMLS CUI [1,1]
C3176590
UMLS CUI [1,2]
C0033975
Patient is on a stable dose of an antipsychotic for at least a month
Description

Pharmaceutical treatment

Data type

boolean

Alias
UMLS CUI [1,1]
C0040615
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
Patient scores 4 or more on at least one item of the positive and negative syndrome scale.
Description

PNNS-Scale

Data type

boolean

Alias
UMLS CUI [1]
C0451383
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
Substance abuse in the past month/dependence past 6 months
Description

Substance abuse / dependence

Data type

boolean

Alias
UMLS CUI [1,1]
C0038586
UMLS CUI [1,2]
C0332185
UMLS CUI [2,1]
C0038580
UMLS CUI [2,2]
C0262926
Patient with history of / or current medical/neurological illnesses e.g. mental retardation (DSM-IV) or epilepsy
Description

Neurological illnesses

Data type

boolean

Alias
UMLS CUI [1]
C2186518
UMLS CUI [2,1]
C0027765
UMLS CUI [2,2]
C0521116
UMLS CUI [3]
C0025362
UMLS CUI [4]
C0014544
Patient with medical conditions that are judged by the consulting internist and research staff to be unstable
Description

Unstable medical conditions

Data type

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0443343
Patient being pregnant or breast-feeding
Description

Pregnancy or breastfeeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
Patient with known allergy or serious adverse event to DEP, received chlorpromazine, trimethoprim or DEP for up to 6 months prior to study entry.
Description

DEP = Depakote = Sodium Valproate

Data type

boolean

Alias
UMLS CUI [1,1]
C0719751
UMLS CUI [1,2]
C0020517
UMLS CUI [2,1]
C0719751
UMLS CUI [2,2]
C1519255
UMLS CUI [3,1]
C0719751
UMLS CUI [3,2]
C2826667
UMLS CUI [4,1]
C0008286
UMLS CUI [4,2]
C2826667
UMLS CUI [5,1]
C0041041
UMLS CUI [5,2]
C2826667
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Similar models

Eligibility

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed consent
Item
Patient signed the written informed consent
boolean
C0021430 (UMLS CUI [1])
Age and gender
Item
Patient is an adult man or woman (aged 18-50 years)
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Diagnosis
Item
Patient with diagnosed schizophrenia or schizoaffective disorder (DSM IV)
boolean
C0011900 (UMLS CUI [1,1])
C0036341 (UMLS CUI [1,2])
C0220952 (UMLS CUI [1,3])
C0011900 (UMLS CUI [2,1])
C0036337 (UMLS CUI [2,2])
C0220952 (UMLS CUI [2,3])
Illness duration
Item
Patient is less than 5 years (since onset of psychosis) ill.
boolean
C3176590 (UMLS CUI [1,1])
C0033975 (UMLS CUI [1,2])
Pharmaceutical treatment
Item
Patient is on a stable dose of an antipsychotic for at least a month
boolean
C0040615 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
PNNS-Scale
Item
Patient scores 4 or more on at least one item of the positive and negative syndrome scale.
boolean
C0451383 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Substance abuse / dependence
Item
Substance abuse in the past month/dependence past 6 months
boolean
C0038586 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
C0038580 (UMLS CUI [2,1])
C0262926 (UMLS CUI [2,2])
Neurological illnesses
Item
Patient with history of / or current medical/neurological illnesses e.g. mental retardation (DSM-IV) or epilepsy
boolean
C2186518 (UMLS CUI [1])
C0027765 (UMLS CUI [2,1])
C0521116 (UMLS CUI [2,2])
C0025362 (UMLS CUI [3])
C0014544 (UMLS CUI [4])
Unstable medical conditions
Item
Patient with medical conditions that are judged by the consulting internist and research staff to be unstable
boolean
C3843040 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
Pregnancy or breastfeeding
Item
Patient being pregnant or breast-feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Contraindication to DEP
Item
Patient with known allergy or serious adverse event to DEP, received chlorpromazine, trimethoprim or DEP for up to 6 months prior to study entry.
boolean
C0719751 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0719751 (UMLS CUI [2,1])
C1519255 (UMLS CUI [2,2])
C0719751 (UMLS CUI [3,1])
C2826667 (UMLS CUI [3,2])
C0008286 (UMLS CUI [4,1])
C2826667 (UMLS CUI [4,2])
C0041041 (UMLS CUI [5,1])
C2826667 (UMLS CUI [5,2])
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