Development of Population Norms of the Computerized Neuropsychological Assessment for Effectiveness of the Antipsychotic Treatment in Schizophrenia
1 other identifier
observational
700
1 country
1
Brief Summary
Schizophrenia affects cognition, emotion, and behavior. Neuropsychological assessment enables a better understanding of antipsychotic effectiveness and the brain processes, underlying cognitive functioning in schizophrenia. Neurocognitive deficits in schizophrenia patients appears to explain up to 61% of the variance of functional outcome and is an important predictor of social reintegration (Peuskens et al, 2005) and independent living activitiy (Green et al, 2004). Impaired social functioning within schizophrenia population has been associated with increased health-care costs. Since social and occupational disability may generate the largest indirect costs of the illness, treatment of cognitive deficits has an enormous impact on the cost and disability associated with schizophrenia (McGurk and Mueser, 2004). However, the gap between cognitive science and clinical practice limits the implementation of cognitive assessment in the routine evaluation of schizophrenia patients. Pharmaceutical industry initiated numerous large scale, multisite studies on the impact of novel antipsychotics on cognitive deficits in schizophrenia patients. The aim of this research is to develop population norms of the computerized neuropsychological assessment for effectiveness of the antipsychotic treatment in schizophrenia.
Trial Health
Trial Health Score
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participants targeted
Target at P75+ for all trials
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2008
CompletedFirst Submitted
Initial submission to the registry
November 11, 2008
CompletedFirst Posted
Study publicly available on registry
November 13, 2008
CompletedNovember 13, 2008
November 1, 2008
November 11, 2008
November 12, 2008
Conditions
Keywords
Study Arms (2)
1
350 healthy women , aged from 18 to 89
2
350 healthy men, aged from 18 to 89
Eligibility Criteria
700 healthy adults (350 women and 350 men, aged from 18 to 89)
You may qualify if:
- An IQ, which is within normal range.
You may not qualify if:
- Psychiatric co-morbidity.
- Physical disability or illness.
- A history of severe head injury.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Beer-Yaacov MHC
Beer Yaacov, 70350, Israel
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER GOV
Study Record Dates
First Submitted
November 11, 2008
First Posted
November 13, 2008
Study Start
July 1, 2008
Last Updated
November 13, 2008
Record last verified: 2008-11