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Clinical Trials/NCT00001323
NCT00001323
Completed
Not Applicable

Neuropsychiatric Evaluation of Normal Subjects and Psychiatric and Neurologic Contrast Groups

National Institute of Mental Health (NIMH)1 site in 1 country810 target enrollmentAugust 1992

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Brain Injury
Sponsor
National Institute of Mental Health (NIMH)
Enrollment
810
Locations
1
Status
Completed
Last Updated
18 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the cognitive processes of participants with schizophrenia, participants with nervous system and mental disorders, and healthy volunteers.

Participants in this study will undergo cognitive tests of attention, memory, attention. Participants with attention deficit hyperactivity disorder (ADHD), traumatic brain injury (TBI), bipolar disorder, and Alzheimer's disease (AD) will be compared with participants with schizophrenia. A group of healthy adults and children will undergo cognitive tests to further delineate the degree of impairment in schizophrenia and neurological disorder participants.

Detailed Description

In this study, we propose to administer cognitive tests to schizophrenic patients and to neurologic patients who will serve as contrast groups for neuropsychological studies of patients with schizophrenia. These include studies of Alzheimers disease to dissociate size and organization of lexicon and ADHD to understand error patterns on CPT-type tests of attention and vigilance. However, the majority of studies will examine schizophrenia in relation to normal controls. In addition, we propose to obtain test results from a local sample of normal subjects of varying ages and educational backgrounds to further delineate degree of impairment in these clinical groups. As well as assessing adults we wish to assess normal children. In particular, we wish to identify in children the size of their lexicon and their degree of semantic organization within their lexicon.

Registry
clinicaltrials.gov
Start Date
August 1992
End Date
August 2005
Last Updated
18 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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