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Cognitive Training
Computerized Cognitive Training for Psychosis (Rem-STEP Trial)
Phase < 1
Recruiting
Led By Ian Ramsay, PhD
Research Sponsored by University of Minnesota
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, one month follow-up post-intervention
Awards & highlights
Summary
This trial will study state representation in young adults with and without a psychiatric diagnosis. The trial will involve some observational tests and a cognitive training clinical trial.
Who is the study for?
This trial is for individuals aged 18-45 with conditions like schizophrenia or mood disorders with psychotic features, fluent in English, and have been stable outside a hospital for at least a month. They must not have severe substance use recently, significant cognitive training experience within the last six months, or other neurological disorders (except autism).
What is being tested?
The study tests two types of computerized cognitive training designed to improve information processing about surroundings in young adults with psychosis compared to those without psychiatric diagnoses.
What are the potential side effects?
Since this trial involves non-invasive computerized cognitive training exercises, there are no direct physical side effects expected from participating. However, participants may experience mental fatigue or stress.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, one month follow-up post-intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, one month follow-up post-intervention
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Performance of Bandit Task Variant
Change in Performance of DPX Task Variant
Secondary study objectives
Brain
Change in Test My Brain Neurocognitive Assessment performance: Matrix Reasoning Z Score
Change in Test My Brain Neurocognitive Assessment performance: Multiracial Emotion Identification Z Score
+2 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: Visual Perception TrainingExperimental Treatment1 Intervention
Contains targeted visual perception exercises from BrainHQ's suite of cognitive exercises. This training paradigm is designed to improve state estimation processes at the perceptual input level.
Group II: Visual Cognitive Control TrainingExperimental Treatment1 Intervention
Contains targeted visual cognitive control exercises from BrainHQ's suite of exercises. This training paradigm is designed to enhance state representation stability of visual information.
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Who is running the clinical trial?
University of MinnesotaLead Sponsor
1,413 Previous Clinical Trials
1,561,303 Total Patients Enrolled
11 Trials studying Psychosis
1,525 Patients Enrolled for Psychosis
National Institute of Mental Health (NIMH)NIH
2,869 Previous Clinical Trials
2,777,436 Total Patients Enrolled
46 Trials studying Psychosis
10,643 Patients Enrolled for Psychosis
Ian Ramsay, PhDPrincipal InvestigatorUniversity of Minnesota Department of Psychiatry and Behavioral Sciences
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am between 18 and 45 years old.I am between 18 and 30 years old.I can make my own decisions about joining a study.I have been diagnosed with a psychotic disorder.I have been diagnosed with a neurological disorder, including autism.I haven't been hospitalized for mental health reasons in the last month.
Research Study Groups:
This trial has the following groups:- Group 1: Visual Perception Training
- Group 2: Visual Cognitive Control Training
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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