Evaluation of a Visual Remediation Intervention for Schizophrenia
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|ClinicalTrials.gov Identifier: NCT03117452|
Recruitment Status : Recruiting
First Posted : April 18, 2017
Last Update Posted : March 30, 2018
|Condition or disease||Intervention/treatment||Phase|
|Schizophrenia||Behavioral: Visual Training||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||40 participants|
|Intervention Model:||Parallel Assignment|
|Intervention Model Description:||Half of the participants will be randomized to receive the computerized visual training, which will be delivered in small groups over a period of 12-14 weeks, and the other half will be assigned to the control condition, which consists of standard Partial Hospital care without visual training.|
|Masking:||Single (Outcomes Assessor)|
|Masking Description:||All participants will be assessed on outcomes of interest by trained clinical interviewers who are blind to the treatment condition in which participants are assigned.|
|Official Title:||Evaluation of a Visual Remediation Intervention for Schizophrenia|
|Actual Study Start Date :||February 23, 2017|
|Estimated Primary Completion Date :||February 28, 2019|
|Estimated Study Completion Date :||February 28, 2019|
Experimental: visual training condition
Participants in the visual training condition will participate in the visual training (VT) group, during which they will complete computerized visual training that targets low- and mid-level visual processes. Each group will include a maximum of 3 participants and will meet 3 times a week over a period of 12-14 weeks.
Behavioral: Visual Training
The computerized visual training (VT) program that is being evaluated was developed by Aaron Seitz, who is a co-investigator on this project; it includes 1) ULTIMEYES, which targets broad-based visual functions, including low-level processes (e.g., visual acuity, contrast sensitivity), and 2) visual perceptual organization exercises, which target mid-level visual processes. Both elements of the program also involve higher-level visual functions, such as visual search and visual attention.
No Intervention: control condition
Participants assigned to the control condition will receive standard Partial Hospital care without visual training.
- contrast sensitivity [ Time Frame: approximately 14 weeks (baseline and post-treatment) ]A measure of low-contrast stimulus detection; contrast sensitivity thresholds at varying spatial frequencies will be examined.
- contour integration [ Time Frame: approximately 14 weeks (baseline and post-treatment) ]A measure of visual perceptual organization; total number correct, adjusted for guessing, will be examined.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03117452
|Contact: Judy L. Thompson, Ph.D.||email@example.com|
|Contact: Steven M. Silverstein, Ph.D.||firstname.lastname@example.org|
|United States, New Jersey|
|Rutgers University Behavioral Health Care (UBHC)||Recruiting|
|Piscataway, New Jersey, United States, 08854|
|Contact: Judy L. Thompson, Ph.D. 732-235-9297 email@example.com|
|Principal Investigator:||Judy L. Thompson, Ph.D.||Rutgers University|