Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Inter-brain synchrony and social connection in schizophrenia

Official title: Inter-Brain Synchrony as a Neural Mechanism of Social Connection in Schizophrenia

Run by University of California, Los Angeles · NCT07177261 · Data updated 2026-11-12

This study will test whether synchronized brain activity between pairs differs for people with schizophrenia compared with people without psychotic disorders, and whether prompting social closeness increases synchrony.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment100 (estimated)
SponsorUniversity of California, Los Angeles
Academic / other
Locations1 site (Los Angeles, California)
StatusRecruiting
StartedNovember 11, 2025
Main results expectedAugust 1, 2027
Study endsNovember 30, 2027
Registry record updatedAugust 11, 2026
Trial IDNCT07177261 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are clinically stable adults with DSM-5 schizophrenia who speak English, are outpatients with no hospitalizations in the prior 3 months and no medication changes in the prior month, or community controls without psychotic or major mood disorders.

Probably not a fit

Patients with IQ under 70 or developmental disability, significant neurological disease or head injury, recent moderate-to-severe substance use, a positive drug screen, or recent sedative/anxiolytic use are excluded and unlikely to benefit from participation.

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

What this trial studies

Researchers will use EEG hyperscanning to record inter-brain synchrony between pairs of participants while they engage in brief social tasks. The protocol compares clinically stable outpatients with a DSM-5 diagnosis of schizophrenia to community control participants without psychotic or major mood disorders. Social closeness will be manipulated using the Fast Friends and Small Talk tasks and synchrony measured before and after the manipulation. The aim is to clarify neural mechanisms of social dysfunction in schizophrenia and provide a basis for new interventions to improve social functioning.

Why it matters

Potential benefit: If successful, findings could identify neural targets for new interventions that improve social connectedness and functioning in schizophrenia.

How similar studies have gone: Prior hyperscanning work in healthy adults has linked inter-brain synchrony to social connection, but this is the first application of that approach in people with schizophrenia.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* sufficient English fluency to comprehend procedures
* clinical group will include individuals with a DSM-5 diagnosis of schizophrenia who are clinically stable (outpatients, with no hospitalizations 3 months prior to enrollment and no medication changes 1 month prior to enrollment)
* members of the community without a psychotic disorder, schizophrenia-spectrum disorder, or current major mood disorder, nor history of a first-degree relative with a psychotic disorder.

Exclusion Criteria:

* evidence of IQ \< 70 or developmental disability
* history of significant neurological disease, serious head injury, or significant current substance use (moderate or severe substance use disorder in the last 3 months, positive urine toxicology screen on the day of assessment, or sedatives/anxiolytics taken within 12 hours of the assessment)

Where it's running

  • University of California, Los Angeles
    Los Angeles, California, United States
    Recruiting

Study contacts

  • Principal investigator: Eric Reavis, Phd — University of California, Los Angeles
  • Study coordinator: Eric Reavis, PhD
  • Email: ereavis@ucla.edu
  • Phone: 310-206-8557

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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.