How timing and sensory predictions are altered in people with schizophrenia
Official title: Sensory and Cognitive Predictions, and Their Disruptions in Schizophrenia
Run by Centre Psychothérapique de Nancy · NCT06361407 · Data updated 2026-11-12
This study tests whether tiny timing changes in a visual motion illusion disrupt sensory prediction more in people with schizophrenia than in people without it.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 60 Years |
| Sex | All |
| Enrollment | 68 (estimated) |
| Sponsor | Centre Psychothérapique de Nancy Academic / other |
| Locations | 2 sites (Marseille and 1 other locations) |
| Status | Recruiting |
| Started | June 28, 2024 |
| Main results expected | October 28, 2027 |
| Study ends | October 28, 2027 |
| Registry record updated | March 25, 2026 |
| Trial ID | NCT06361407 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–60 with a diagnosis of schizophrenia who can give informed consent, have adequate vision, and meet the study's exclusion criteria are ideal candidates.
✕Probably not a fit
People with recent substance use disorders, significant neurological disease, severe visual impairment, certain personality disorders, or those who are pregnant or otherwise ineligible are unlikely to benefit from participating.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Participants view an illusion where two moving squares collide and disappear while subtle timing perturbations (millisecond-scale accelerations and rebounds) are introduced during their trajectories. Neurotypical observers normally perceive a brief gap at collision because sensory predictions create a mismatch when contrast disappears, and this task measures that prediction error. The study compares responses from adults with schizophrenia to those of controls to see if patients are abnormally sensitive to trajectory changes. Behavioral responses to the illusion will be used to probe differences in sensory prediction and timing processing.
Why it matters
Potential benefit: If successful, the work could improve understanding of how disrupted sensory prediction contributes to psychotic symptoms and help develop objective tests or targets for treatment.
How similar studies have gone: Previous experiments have shown the collision illusion and altered timing/prediction in schizophrenia, and this study builds on that prior work by introducing novel millisecond-scale perturbations.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male or female; * Age between 18 and 60 inclusive; * Subject having dated and signed the consent form prior to the start of any trial-related procedure (guardian or curator where applicable); * Member of a social security scheme or beneficiary of such a scheme. Exclusion Criteria: * Psychoactive substance use disorders (as defined by the DSM-V) (Diagnostic and Statistical Manual-V); * Use of benzodiazepines, hallucinogens (in the period preceding before inclusion, for a duration equivalent to 5 half-lives of the product) or cannabis (in the 2 months preceding inclusion); * Neurological pathology or sequelae; * Attention deficit hyperactivity disorder (ADHD); * Borderline personality disorder; * Disabling sensory disorders (visual acuity \<0.8); * Person deprived of liberty or under court protection; * Pregnant, parturient or breast-feeding women; * Subjects in a period of exclusion defined by another clinical study.
Where it's running
-
CHU Sainte Marguerite, APHM
Marseille, France Recruiting -
Centre Hospitalier Drôme Vivarais
Montéléger, France Recruiting
Study contacts
- Principal investigator: Anne Giersch, MD PhD — Institut National de la Santé Et de la Recherche Médicale, France
- Study coordinator: Anne Giersch, MD PhD
- Email: giersch@unistra.fr
- Phone: 0033 3 88 116471
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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.