Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
NCT07469384

Non-invasive Brain Stimulation Using Tdcs of the Third (of Many) Visual Pathways

Led by Nathan Kline Institute for Psychiatric Research · Updated on 2026-03-13

120

Participants Needed

1

Research Sites

230 weeks

Total Duration

On this page

Sponsors

N

Nathan Kline Institute for Psychiatric Research

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study investigates the ability of transcranial direct current stimulation (tDCS) applied over the motion processing area of the brain (area MT) to improve face emotion recognition (FER) ability. tDCS is a type of non-invasive brain stimulation in which low level currents are applied over the scalp to influence underlying brain function. In schizophrenia, impaired ability to detect facial motion has been shown to contribute to impaired FER, which, in turn, leads to difficulties in social cognition and poor social outcome. The study will use both fMRI and EEG to measure brain function while participants view moving dot and dynamic face stimuli. Analyses will compare changes in fMRI and EEG activity in individuals receiving active vs. sham stimulation.

CONDITIONS

Official Title

Non-invasive Brain Stimulation Using Tdcs of the Third (of Many) Visual Pathways

Who Can Participate

Age: 18Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female subject, age 18-55
  • Competent and willing to sign informed consent
  • No more than moderately ill
  • SCID DSM-5 diagnosis of schizophrenia or schizoaffective disorder
  • WAIS IQ greater than 70
  • No current or recent (past 6 months) DSM-5 substance abuse or dependence
  • On medication within clinically approved range
  • Does not have other DSM-5 disorders except minor ones such as simple phobia
Not Eligible

You will not qualify if you...

  • Significant neurological illness or history of significant head trauma
  • Unstable physical illness or significant auditory/visual deficits that might interfere
  • Contraindication to MRI (e.g., metal implants, claustrophobia, pregnancy)
  • Contraindications to tDCS including metal implant, pacemaker, history of seizure, traumatic brain injury, or stroke
  • Significant risk for suicide
  • History of illness or condition that may interfere with study completion or data quality
  • Moderate or greater current DSM-5 substance use disorder or substance use impacting daily activities

AI-Screening

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Trial Site Locations

Total: 1 location

1

Nathan Kline Institute

Orangeburg, New York, United States, 10962

Actively Recruiting

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Research Team

O

Odeta Beggel, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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