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Measuring Visual Brain Responses in People With Psychotic Disorders

Uses EEG brain recordings to look for markers of psychosis in adults.

Plain-language title generated from the registry record
Registry title: Visual Perception in Schizophrenia

Key facts

Where
Rochester, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT06911931, who can take part

Where in United States

  • University of RochesterRochester, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University of Rochester
Trial code
NCT06911931
Record updated
12 November 2025
Original description
This study aims to identify novel markers of psychosis using electroencephalography (EEG).Read full original descriptionShow less

Visual Perception in Schizophrenia: Assessing Predictive Processing in the Earliest Stages of the Visual Cortical Hierarchy

This study aims to identify novel markers of psychosis using electroencephalography (EEG).

Inclusion: All Subjects; Aged 18-65; 20/32 visual acuity or better (using in-house optical correction, if necessary); An ability to speak English well enough to complete study assessments and to consent to the study; Subjects with Schizophrenia-Spectrum Disorder; Meets DSM-5 diagnostic criteria for schizophrenia, schizoaffective disorder, or schizophreniform disorder as confirmed by the Structured Interview for DSM-5 (SCID-5); Subjects with Bipolar Disorder; Meets DSM-5 diagnostic criteria for bipolar disorder (type I, II, or unspecified) as confirmed by the Structured Interview for DSM-5 (SCID-5).

Exclusion: Presence of characteristics that could impair one's ability to comprehend the nature of the study, provide informed consent, or understand the assessment questions, including the following:; Subject cannot read and understand the instructions well enough to complete the tasks or cannot provide informed consent; Intellectual impairment (WRAT-5 score < 70) (at the discretion of experimenter); Actively intoxicated, as shown via patient self-report or staff report; Substance use disorder in the past 3 months; Subject considered high risk for suicidal acts (i.e., active suicidal ideation as determined by clinical interview OR any suicide attempt in 30 days prior to screening); Subject violence (involving severe/lethal means or violence occurring in prior 6 months) or extreme agitation; Being in a current manic state; Head injury with loss of consciousness greater than 10 minutes (at the discretion of the experimenter); Subject has had electroconvulsive therapy (ECT) in the past 8 weeks; Diagnosed with a neurological condition (tumor, stroke, brain injury) or neurological disorder, including seizure disorders. Diagnosed with pervasive developmental disorder (phone screen or medical records); Lazy eye or squint or other known ocular pathology; Daily antidepressant, mood stabilizer or antipsychotic medication use in the last 6 months, or benzodiazepine use during the prior 2 days (self-disclosure); iii. First-degree relative(s) with a schizophrenia spectrum disorder (based on subject self-report) or bipolar disorder; Daily antidepressant, mood stabilizer or antipsychotic medication use in the last 6 months, or benzodiazepine use during the prior 2 days; Any lifetime psychotic disorder or history of psychiatric hospitalization (self disclosure); Any lifetime psychotic disorder (as assessed by SCID/or SSD); History of psychiatric hospitalization; First-degree relative(s) with a schizophrenia spectrum disorder (based on subject self-report) or bipolar disorder; All subjects; Healthy Control Subjects; Case-match Control Non-ill Subjects; Recurrent depressive episodes or being in a current depressive episode (as assessed by SCID/or SSD); Persistent threshold psychotic symptoms; Bipolar Subjects; Persistent threshold psychotic symptoms.

ClinicalTrials.gov NCT06911931