ID

23085

Description

Effectiveness of Antipsychotic Combination With Psychosocial Intervention on Outcome of Patients With Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT00654576

Link

https://clinicaltrials.gov/show/NCT00654576

Keywords

  1. 6/22/17 6/22/17 -
Uploaded on

June 22, 2017

DOI

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License

Creative Commons BY 4.0

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Eligibility Schizophrenia NCT00654576

Eligibility Schizophrenia NCT00654576

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
eligible patients were 16 to 50 years of age;
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
had received a diagnosed of schizophrenia in accordance with criteria set out in the diagnostic and statistical manual of mental disorders-fourth edition (dsm-iv);
Description

Schizophrenia

Data type

boolean

Alias
UMLS CUI [1]
C0036341
were confirmed to be clinically stable by the investigator (the total score ≤60 on the positive and negative syndrome scale [panss] or a decrease of fifty percent from acute period in the total score on panss)
Description

PANSS Stable status Clinical | PANSS Decrease Percentage

Data type

boolean

Alias
UMLS CUI [1,1]
C0451383
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C0205210
UMLS CUI [2,1]
C0451383
UMLS CUI [2,2]
C0547047
UMLS CUI [2,3]
C0439165
and taken maintenance treatment with any one of the following seven oral antipsychotics:
Description

Oral antipsychotic therapy Maintenance

Data type

boolean

Alias
UMLS CUI [1,1]
C4273790
UMLS CUI [1,2]
C0024501
chlorpromazine
Description

Chlorpromazine

Data type

boolean

Alias
UMLS CUI [1]
C0008286
sulpiride clozapine
Description

Sulpiride | Clozapine

Data type

boolean

Alias
UMLS CUI [1]
C0038803
UMLS CUI [2]
C0009079
risperidone
Description

Risperidone

Data type

boolean

Alias
UMLS CUI [1]
C0073393
olanzapine
Description

olanzapine

Data type

boolean

Alias
UMLS CUI [1]
C0171023
quetiapine
Description

quetiapine

Data type

boolean

Alias
UMLS CUI [1]
C0123091
aripiprazole
Description

aripiprazole

Data type

boolean

Alias
UMLS CUI [1]
C0299792
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients were excluded if they had received a diagnosis of schizoaffective disorder, mental retardation, or other cognitive disorders;
Description

Schizoaffective Disorder | Mental Retardation | Cognition Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0036337
UMLS CUI [2]
C0025362
UMLS CUI [3]
C0009241
had a history of serious adverse reactions to the proposed treatment;
Description

Adverse reactions Serious

Data type

boolean

Alias
UMLS CUI [1,1]
C0559546
UMLS CUI [1,2]
C0205404
were pregnant or breastfeeding; or had a serious and unstable medical condition.
Description

Pregnancy | Breast Feeding | Medical condition Serious Unstable

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3843040
UMLS CUI [3,2]
C0205404
UMLS CUI [3,3]
C0443343
patients were excluded if they were unable to provide informed consent
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582

Similar models

Eligibility Schizophrenia NCT00654576

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
eligible patients were 16 to 50 years of age;
boolean
C0001779 (UMLS CUI [1])
Schizophrenia
Item
had received a diagnosed of schizophrenia in accordance with criteria set out in the diagnostic and statistical manual of mental disorders-fourth edition (dsm-iv);
boolean
C0036341 (UMLS CUI [1])
PANSS Stable status Clinical | PANSS Decrease Percentage
Item
were confirmed to be clinically stable by the investigator (the total score ≤60 on the positive and negative syndrome scale [panss] or a decrease of fifty percent from acute period in the total score on panss)
boolean
C0451383 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
C0451383 (UMLS CUI [2,1])
C0547047 (UMLS CUI [2,2])
C0439165 (UMLS CUI [2,3])
Oral antipsychotic therapy Maintenance
Item
and taken maintenance treatment with any one of the following seven oral antipsychotics:
boolean
C4273790 (UMLS CUI [1,1])
C0024501 (UMLS CUI [1,2])
Chlorpromazine
Item
chlorpromazine
boolean
C0008286 (UMLS CUI [1])
Sulpiride | Clozapine
Item
sulpiride clozapine
boolean
C0038803 (UMLS CUI [1])
C0009079 (UMLS CUI [2])
Risperidone
Item
risperidone
boolean
C0073393 (UMLS CUI [1])
olanzapine
Item
olanzapine
boolean
C0171023 (UMLS CUI [1])
quetiapine
Item
quetiapine
boolean
C0123091 (UMLS CUI [1])
aripiprazole
Item
aripiprazole
boolean
C0299792 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Schizoaffective Disorder | Mental Retardation | Cognition Disorders
Item
patients were excluded if they had received a diagnosis of schizoaffective disorder, mental retardation, or other cognitive disorders;
boolean
C0036337 (UMLS CUI [1])
C0025362 (UMLS CUI [2])
C0009241 (UMLS CUI [3])
Adverse reactions Serious
Item
had a history of serious adverse reactions to the proposed treatment;
boolean
C0559546 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Medical condition Serious Unstable
Item
were pregnant or breastfeeding; or had a serious and unstable medical condition.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3843040 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
C0443343 (UMLS CUI [3,3])
Informed Consent Unable
Item
patients were excluded if they were unable to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])

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