Remediation of Visual Perceptual Impairments in People With Schizophrenia
NCT03314129 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 79
Last updated 2025-09-05
Summary
The purpose of this study is to evaluate the effectiveness of a visual remediation intervention for people with schizophrenia. The intervention targets two visual functions that much research has shown are impaired in many people with the disorder, namely contrast sensitivity and perceptual organization. The first phase of the study will test the effects of interventions targeting each of these processes, as well as the effects of a combined package. A control condition of higher-level cognitive remediation is included as a fourth condition. The second phase of the study will evaluate the effectiveness of the most effective intervention from the first phase, but in a new and larger sample of individuals. Outcome measures include multiple aspects of visual functioning, as well as visual cognition and overall community functioning.
Conditions
- Schizophrenia
- Schizoaffective Disorder
Interventions
- BEHAVIORAL
-
UltimEyes
A computer program developed to improve contrast sensitivity and visual acuity.
- BEHAVIORAL
-
Contour Integration Training
A computerized program to improve contour integration (a form of perceptual organization).
- BEHAVIORAL
-
UltimEyes + Contour Integration Training
The combination of UltimEyes and Contour Integration Training
- BEHAVIORAL
-
MyBrainSolutions
A computer program consisting of exercises to improve cognition (attention, memory, planning) and to facilitate goal setting.
Sponsors & Collaborators
-
New York University
collaborator OTHER -
Weill Medical College of Cornell University
collaborator OTHER -
National Institute of Mental Health (NIMH)
collaborator NIH -
University of Rochester
lead OTHER
Principal Investigators
-
Steven M Silverstein, Ph.D. · University of Rochester
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-06-01
- Primary Completion
- 2025-03-31
- Completion
- 2025-05-31
Countries
- United States
Study Locations
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