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NCT Number: NCT06458153

Imaging Speech in Neurotypical Adults and Individuals With Cerebellar Stroke

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).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Pittsburgh

Pittsburgh, Pennsylvania, 15260, United States

Location status: Recruiting

Location contact

Alexander Ocampo, BA

CONTACT

[email protected]

Jason Bohland, Ph.D.

CONTACT

[email protected]

412-383-3416

Jason W Bohland, Ph.D.

PRINCIPAL_INVESTIGATOR

About this study

This study aims to provide an integrated view of brain systems underlying predictive coding in speech with unprecedented detail using ultra-high field (7 Tesla) functional magnetic resonance imaging. The overall approach is a condition-intensive within-subjects design, with extensive sampling of individual participants, including a group who have had strokes impacting the cerebellum, across multiple sessions.

Participants will be asked to complete up to 6 sessions. Passing a hearing assessment using standard audiological procedures, conducted at the start of the first session, is a requirement for participation. The experimental sessions involve behavior and non-invasive brain imaging.

Investigators will ask participants to perform several short tasks to measure different aspects of their speech production and speech perception (e.g., reading passages or words aloud, making judgements about sounds).

In one session, Investigators will measure electroencephalography (EEG) while participants complete tasks involving producing and hearing speech sounds. Participants will be fitted with an elastic cap and up to 32 non-invasive recording electrodes.

In other sessions, investigators will measure structural and functional magnetic resonance imaging (fMRI). Structural images demonstrate the unique brain anatomy of the participant. Functional images will be obtained while the participant completes specific tasks involving listening, speaking, or completing other motor actions (e.g., pressing a button). All participants will be screened for MRI risk factors prior to each session.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Cohort 1 (neurotypical adults):

  • Age 18-49
  • Right-handed
  • Native English speaker

Cohort 2 (people with cerebellar lesions):

  • Age 18 or older
  • Right-handed
  • Native English speaker
  • History of cerebellar stroke

Cohort 3 (controls matched to Cohort 2)

  • Age 18 or older
  • Right-handed
  • Native English speaker

Exclusion criteria

Cohort 1 (neurotypical adults):

  • Presence of MRI risk factors: metal and/or electromagnetic devices (e.g., pacemakers, neurostimulators) in the body, previous shrapnel injuries, use of an intrauterine device containing metal, claustrophobia, pregnant or possibly pregnant
  • History of neurological / neurodegenerative disease or severe brain injury (e.g., stroke or severe traumatic brain injury)
  • Hearing loss, defined by pure tone thresholds >25 decibels (dB) hearing level (HL) at octave frequencies between 250-8000 Hz
  • Clinical diagnosis and/or treatment for schizophrenia or other psychotic disorders
  • Clinical diagnosis and/or treatment for neurocognitive disorders (e.g., dementia, delirium)
  • Presence of a severe and unmanaged, clinically diagnosed attention disorder
  • Clinically diagnosed with or treated for a speech, language, or hearing disorder
  • Head circumference greater than 60cm or weight greater than 300 pounds
  • History of severe claustrophobia
  • Currently pregnant

Cohort 2 (people with cerebellar lesions):

  • Presence of MRI risk factors: metal and/or electromagnetic devices (e.g., pacemakers, neurostimulators) in the body, previous shrapnel injuries, use of an intrauterine device containing metal, claustrophobia, pregnant or possibly pregnant
  • History of neurological / neurodegenerative disease or severe brain injury other than stroke
  • Hearing loss, defined by pure tone thresholds >50 dB HL at octave frequencies between 250-4000 Hz
  • Clinical diagnosis and/or treatment for schizophrenia or other psychotic disorders
  • Clinical diagnosis and/or treatment for neurocognitive disorders (e.g., dementia, delirium)
  • Presence of a severe and unmanaged, clinically diagnosed attention disorder
  • Head circumference greater than 60cm or weight greater than 300 pounds
  • History of severe claustrophobia
  • Currently pregnant

Cohort 3 (controls matched to Cohort 2):

  • Presence of MRI risk factors: metal and/or electromagnetic devices (e.g., pacemakers, neurostimulators) in the body, previous shrapnel injuries, use of an intrauterine device containing metal, claustrophobia, pregnant or possibly pregnant
  • History of neurological / neurodegenerative disease or severe brain injury (e.g., stroke or severe traumatic brain injury)
  • Hearing loss, defined by pure tone thresholds >50 dB HL at octave frequencies between 250-4000 Hz
  • Clinical diagnosis and/or treatment for schizophrenia or other psychotic disorders
  • Clinical diagnosis and/or treatment for neurocognitive disorders (e.g., dementia, delirium)
  • Presence of a severe and unmanaged, clinically diagnosed attention disorder
  • Clinically diagnosed with or treated for a speech, language, or hearing disorder
  • Head circumference greater than 60cm or weight greater than 300 pounds
  • History of severe claustrophobia
  • Currently pregnant

Treatment and study plan

Neural responses to speech functional localizer

Behavioral

Measuring speech-related brain activity using fMRI during a speech listening task.

Neural responses to silent articulation

Behavioral

Measuring speech-related brain activity using fMRI during a silent articulation task.

Neural responses to self vs. externally generated speech

Behavioral

Measuring speech-related brain activity using fMRI during self-generated vs. externally-generated speech.

Event-related potentials for speech

Behavioral

Measuring electroencephalography (EEG) based evoked potentials for self vs. externally generated speech

Neural responses to induced speech errors

Behavioral

Measuring speech-related brain activity using fMRI during conditions that induce auditory speech errors.

Neural responses to sensory-motor adaptation

Behavioral

Measuring brain activity using fMRI during a learning task with sustained altered auditory feedback.

Speech production behaviors

Behavioral

Behavioral measurements of speech during reading passages and words

Auditory acuity testing

Behavioral

Measurements of auditory acuity during listening tasks.

Neural responses to learning a non-speech auditory motor behavior

Behavioral

Mapping of brain areas using fMRI during learning of non-speech sound-evoking movements.

Primary outcomes

  1. Blood oxygenation level dependent (BOLD) responses to self vs. externally generated speech

    Time frame: One session lasting 2-3 hours, within 12 months of enrollment

    The dependent variables (across voxels) are blood oxygenated level dependent fMRI measurements made during task performance. We will contrast measured activations in regions of interest for the LISTEN-SELF vs. PRODUCE and LISTEN-OTHER vs. PRODUCE conditions. Encoding models will predict activity in regions-of-interest (ROIs) based on a set of speech features.

  2. BOLD responses related to pre-speech auditory modulation

    Time frame: One session lasting 2-3 hours, within 12 months of enrollment

    The dependent variables (across voxels) are blood oxygenated level dependent fMRI measurements made during task performance. We will contrast measured activations in regions of interest for responses to auditory stimuli across conditions (e.g., SPEAK, REHEARSE, PLAN, SILENT).

  3. EEG responses to self vs. externally generated speech

    Time frame: One session lasting 2-3 hours, within 12 months of enrollment

    The dependent variables are evoked responses, aligned to sound onset, measured with EEG during task performance. We will contrast evoked responses across conditions (e.g., TALK, LISTEN).

  4. BOLD responses to induced auditory errors

    Time frame: One session lasting 2-3 hours, within 12 months of enrollment

    The dependent variables (across voxels) are blood oxygenated level dependent fMRI measurements made during task performance. We will determine activations in regions of interest that correlate with applied perturbations during speech. We will also compare SPEAK vs. LISTEN activations in perturbed and unperturbed conditions.

  5. BOLD responses during adaptation to auditory perturbations

    Time frame: One session lasting 2-3 hours, within 12 months of enrollment

    The dependent variables (across voxels) are blood oxygenated level dependent fMRI measurements made during task performance. We will contrast measured activations in regions of interest for responses during the HOLD and BASELINE phases of the adaptation paradigm. We will determine areas where activation is associated with changes in formant frequencies in early and late windows in speech recordings.

  6. BOLD responses during learning of non-speech auditory motor targets

    Time frame: One session lasting 2-3 hours, within 12 months of enrollment

    The dependent variables (across voxels) are blood oxygenated level dependent fMRI measurements made during task performance. We will contrast measured activations in regions of interest for responses during PRESS trials across runs. We will contrast LISTEN vs. PRESS trials to measure motor induced sensory modulation.

Secondary outcomes

  1. BOLD responses to speech listening task

    Time frame: One session lasting 2-3 hours, within 12 months of enrollment

    The dependent variables (across voxels) are blood oxygenated level dependent fMRI measurements made during task performance. We will contrast measured activations for the SPEECH vs. signal correlated noise (SCN) and SPEECH vs. SILENT conditions.

  2. BOLD responses to silent articulation task

    Time frame: One session lasting 2-3 hours, within 12 months of enrollment

    The dependent variables (across voxels) are blood oxygenated level dependent fMRI measurements made during task performance. We will contrast measured activations for silent articulation vs. a resting baseline condition.

  3. Speech formant frequencies

    Time frame: First session lasting 2-3 hours, within 12 months of enrollment

    We will measure participant-specific phonetic variables (formant frequencies) based on participant speech from reading passages and word production.

  4. Spontaneous Speech Synchronization Index

    Time frame: First session lasting 2-3 hours, within 12 months of enrollment

    We will measure the Spontaneous Speech Synchronization Index based on behavioral speech data.

  5. Auditory acuity

    Time frame: First session lasting 2-3 hours, within 12 months of enrollment

    We will measure auditory acuity (just noticeable difference) for changes in formant frequencies based on behavioral speech samples.

Study contacts

Contact information is provided by the study sponsor or research team.

Alexander Ocampo, B.A.

CONTACT

[email protected]

Jason W Bohland, Ph.D.

CONTACT

[email protected]

412-383-3416

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Collaborators

  • National Institute on Deafness and Other Communication Disorders (NIDCD)
  • Northwestern University

Registry information

Official study title

High-resolution Functional Imaging of Speech-induced Sensory Modulation

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Jun 13, 2024
Registry last updated
Jun 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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