State Representation in Early Psychosis 2
Run by University of Minnesota · NCT07834203 · Data updated 2026-11-12
This observational study tests how people with early psychosis and healthy individuals use state information during tasks and how brain activity supports it.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 15 Years to 45 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | University of Minnesota Academic / other |
| Locations | 2 sites (Minneapolis, Minnesota and 1 other locations) |
| Status | Recruiting |
| Started | October 15, 2025 |
| Main results expected | June 30, 2030 |
| Study ends | June 30, 2030 |
| Registry record updated | September 22, 2026 |
| Trial ID | NCT07834203 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are ages 15–45 with early psychosis or healthy controls matched on demographics and language proficiency.
✕Probably not a fit
Participants who do not show detectable biomarkers or who do not complete task sessions may not contribute to biomarker development.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study compares behavioral performance, computational measures, and EEG signals related to state representation in people with early psychosis and matched healthy controls. Participants complete interviews, self-report measures, cognitive tests, computer-based tasks, and EEG during task performance and rest. The goal is to identify neurocognitive and neurophysiologic markers that could inform future precision psychiatry approaches. Data will be analyzed to relate computational task parameters, EEG markers, and clinical outcomes. It is conducted under an NIH Conte Center grant at University of Minnesota with collaboration from NIMH.
Why it matters
Potential benefit: If successful, the study could identify biomarkers and cognitive profiles that help tailor treatments for early psychosis.
How similar studies have gone: Prior work has shown useful links between EEG markers and cognitive control in psychosis, supporting this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: All participants: * Aged between 15 and 45 years * English proficiency, as determined by staff observation and participant self-report * Estimated IQ at or above 70, as estimated by cognitive assessments * Estimated visual acuity at 20/40, as estimated by the visual acuity test Early Psychosis participants: * Clinical diagnosis of schizophrenia, schizoaffective disorder, schizophreniform disorder, psychosis NOS, bipolar disorder with psychosis, or major depressive disorder with psychosis * Age 35 years or younger, or age 36 to 45 years with onset of psychotic symptoms within the previous 5 years * Achieved clinical stability, defined as outpatient status for at least one month prior to study participation Exclusion Criteria: All participants: * Unable or unwilling to provide informed consent * Unable to demonstrate adequate decisional capacity, in the judgment of the consenting study staff member * Illiterate * Previous clinically significant head injury or prolonged unconsciousness, as determined by the investigators * Meets criteria for severe substance or alcohol use disorder within 3 months of behavioral assessment * Presence of any major medical condition that, in the opinion of the investigators, would impede participation or put the participant at additional risk * Has participated in significant formal cognitive training programs, as determined by the investigators * Meets criteria for clinical risk of suicidal behavior Early Psychosis participants: \- Presence of a major neurological disorder Healthy Control participants: * Meets DSM-5 criteria for psychotic or bipolar disorder * Has a first-degree family history of psychotic or bipolar disorder * Presence of a major neurological disorder
Where it's running
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University of Minnesota Ambulatory Research Center
Minneapolis, Minnesota, United States Recruiting -
University of Minnesota Department of Psychology
Minneapolis, Minnesota, United States Recruiting
Study contacts
- Principal investigator: Scott Sponheim, PhD, LP — University of Minnesota
- Study coordinator: Grace Owens
- Email: step2study@umn.edu
- Phone: (612) 741-2826
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.