Clinical trial Recruiting at 1 site Observational Ages 18 to 60

Exploring social dysfunction in schizophrenia through brain activity

Official title: HYEEG Discourse in Psychosis: A Neurobehavioural Study

Run by Douglas Mental Health University Institute · NCT06978803 · Data updated 2026-11-12

This study is trying to see how brain activity during social interactions affects communication and social skills in people with schizophrenia.

Quick facts

Study typeObservational
Ages18 Years to 60 Years
SexAll
Enrollment110 (estimated)
SponsorDouglas Mental Health University Institute
Academic / other
Locations1 site (Montreal, Quebec)
StatusRecruiting
StartedJanuary 16, 2024
Main results expectedOctober 22, 2025
Study endsDecember 31, 2026
Registry record updatedMay 18, 2025
Trial IDNCT06978803 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are English or French-speaking individuals aged 18-60 with a diagnosis of schizophrenia or schizoaffective disorder and less than 5 years since illness onset.

Probably not a fit

Patients with primary diagnoses of substance abuse, severe medical disorders, or neurological conditions affecting speech may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study investigates the mechanisms of social dysfunction in individuals with schizophrenia by examining the relationship between disorganized communication and social interaction. Participants will engage in structured social interactions while undergoing dual-brain EEG hyperscanning to measure neural and behavioral synchrony. The study aims to identify measurable markers of disorganized communication and link them to clinical symptoms and social functioning, focusing on aspects such as motor imitation and verbal coherence.

Why it matters

Potential benefit: If successful, this study could lead to improved understanding and interventions for social dysfunction in patients with schizophrenia.

How similar studies have gone: While the specific approach of dual-brain EEG hyperscanning is relatively novel, similar studies have shown promise in understanding social cognition in psychiatric disorders.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. English or French-speaking participants (as dyads matched for language preference).
2. Ages 18-60 years.
3. Patients meeting the operational criteria for schizophrenia or schizoaffective illness as previously diagnosed by their treating psychiatrist, based on the Diagnostic and Statistical Manual of Mental Disorders (DSM) 5 criteria (Zipursky et al., 2020).
4. Patients with less than 5 years of illness onset, based on the time of starting treatment with antipsychotic medication.

Exclusion Criteria:

1. Participants should not have a primary diagnosis of Alcohol or Drug abuse or addiction (however, co-morbid substance abuse with a primary diagnosis of psychotic disorder is not an exclusion criterion).
2. Participants should not have a severe medical disorder that would explain psychotic symptoms.
3. Participants should not have a past or current history of a primary neurological disorder that can affect speech output
4. Participants with IQ below 70 or a concurrent pervasive developmental disorder (e.g., autism) will also be excluded.

Where it's running

  • Douglas Mental Health University Institute
    Montreal, Quebec, Canada
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.