Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06458153

Imaging Speech in Neurotypical Adults and Individuals With Cerebellar Stroke

Led by University of Pittsburgh · Updated on 2025-06-13

100

Participants Needed

1

Research Sites

161 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

N

Northwestern University

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this research study is to learn how the brain areas that plan and control movement interact with the areas responsible for hearing and perceiving speech in healthy adults and people who have had cerebellar strokes. The main questions it aims to answer are: 1. What regions of the brain's sensory systems show changes in their activity related to speech? 2. To what extent do these regions help listeners detect and correct speech errors? 3. What is the role of the cerebellum (a part of the brain in the back of the head) in these activities? Participants will be asked to complete several experimental sessions involving behavioral speech and related tests and non-invasive brain imaging using electroencephalography (EEG) and functional magnetic resonance imaging (fMRI).

CONDITIONS

Official Title

Imaging Speech in Neurotypical Adults and Individuals With Cerebellar Stroke

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Cohort 1 (neurotypical adults): Age 18 to 49 years
  • Cohort 1: Right-handed
  • Cohort 1: Native English speaker
  • Cohort 2 (people with cerebellar lesions): Age 18 years or older
  • Cohort 2: Right-handed
  • Cohort 2: Native English speaker
  • Cohort 2: History of cerebellar stroke
  • Cohort 3 (controls matched to Cohort 2): Age 18 years or older
  • Cohort 3: Right-handed
  • Cohort 3: Native English speaker
Not Eligible

You will not qualify if you...

  • Presence of MRI risk factors such as metal or electromagnetic devices in the body, previous shrapnel injuries, use of intrauterine device containing metal, claustrophobia, or pregnancy
  • History of neurological or neurodegenerative disease or severe brain injury (e.g., stroke, traumatic brain injury) except for cerebellar stroke in Cohort 2
  • Hearing loss greater than 25 dB hearing level at octave frequencies 250-8000 Hz for Cohort 1
  • Hearing loss greater than 50 dB hearing level at octave frequencies 250-4000 Hz for Cohorts 2 and 3
  • Clinical diagnosis or treatment for schizophrenia or other psychotic disorders
  • Clinical diagnosis or treatment for neurocognitive disorders such as dementia or delirium
  • Presence of severe and unmanaged clinically diagnosed attention disorder
  • Clinical diagnosis or treatment for speech, language, or hearing disorders (except for Cohort 2)
  • Head circumference greater than 60 cm or weight greater than 300 pounds
  • History of severe claustrophobia
  • Currently pregnant or possibly pregnant

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15260

Actively Recruiting

Loading map...

Research Team

J

Jason W Bohland, Ph.D.

CONTACT

A

Alexander Ocampo, B.A.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here