Oculomotor and Spatial Cognition Deficits in Schizophrenia

NCT ID: NCT00931996

Last Updated: 2013-01-24

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-06-30

Study Completion Date

2011-11-30

Brief Summary

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DESCRIPTION: (Verbatim from the Applicant's Abstract) Abnormalities of eye movement control and spatial cognition are well-established deficits in schizophrenia. However, the regional disturbances in brain function causing these deficits are not yet known. This application proposes a series of integrated behavioral studies designed to identify causes of deficits in schizophrenia.

Detailed Description

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We will be assessing clinical symptoms and cognition before and after treatment.

Conditions

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Schizophrenia

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Antipsychotic

Antipsychotic

Group Type EXPERIMENTAL

Antipsychotic

Intervention Type DRUG

Risperidone is the first line antipsychotic followed by others per clinician choice. Flexible dosing QD x 4-6 weeks.

Interventions

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Antipsychotic

Risperidone is the first line antipsychotic followed by others per clinician choice. Flexible dosing QD x 4-6 weeks.

Intervention Type DRUG

Eligibility Criteria

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Exclusion Criteria

* Any subject is excluded from the imaging studies if they have any contraindications to MRI such as cardiac pacemaker, aneurysm clip, cochlear implants, pregnancy in the later stages (because of body size and limited comfort for MRI studies), IUD, shrapnel, history of metal fragments in eyes, neurostimulators, weight of 250 lbs. or more, or claustrophobia. Individuals with mental retardation, neurologic disease or significant medical illness that might effect neuronal or vascular physiology will not be recruited.
Minimum Eligible Age

15 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

University of Illinois at Chicago

OTHER

Sponsor Role lead

Responsible Party

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Jeffrey R. Bishop

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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John A Sweeney, PhD

Role: PRINCIPAL_INVESTIGATOR

UIC/UTSW

Locations

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UIC Center for Cognitive Medicine

Chicago, Illinois, United States

Site Status

Countries

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United States

Other Identifiers

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R01MH062134

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R01MH080066

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2001-0522

Identifier Type: -

Identifier Source: org_study_id

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