Neural Mechanisms for Stopping Ongoing Speech Production (Study 2)
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Speech Production Tasks.
- Who it may be relevant to
- Registry conditions: Epilepsy, Speech. Basic parameters: 8 years — 26 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Speech and communication disorders often result in aberrant control of the timing of speech production, such as making improper stops at places where they should not be. During normal speech, the ability to stop when necessary is important for maintaining turn-taking in a smooth conversation. Existing studies have largely investigated neural circuits that support the preparation and generation of speech sounds. It is believed that activity in the prefrontal and premotor cortical areas facilitates high-level speech control and activity in the ventral part of the sensorimotor cortex controls the articulator (e.g. lip, jaw, tongue) movements. However, little is known about the neural mechanism controlling a sudden and voluntary stop of speech. Traditional view attributes this to a disengagement of motor signals while recent evidence suggested there may be an inhibitory control mechanism. This gap in knowledge limits our understanding of disorders like stuttering and aphasia, where deficits in speech timing control are among the common symptoms. The overall goal of this study is to determine how the brain controls the stopping of ongoing speech production to deepen our understanding of speech and communication in normal and impaired conditions.
Detailed description
Intracranial electroencephalography (iEEG) is a state-of-the-art technique with fine spatial and temporal resolutions that are well suited for studying the neural dynamics of speech. This study proposes to assess speech production in patients who are undergoing iEEG recording to carry out clinical procedures for indications related to their medical condition. The research study team will investigate neural signals correlated with speech stopping using speech production and stopping tasks with visual cues. The research study team will compare effects on neural activity within each individual subject and identify common patterns of activity across subjects. The aims of this study seek to determine the role of the premotor network for stopping during naturalistic usage. This study will provide basic knowledge for the precise control of speech stopping and the control of speech timing in general, bridging the current speech production studies to real-world communication conditions, and help inspire new theories of speech motor control.
Interventions
- Behavioral Speech Production Tasks
View visual cues and undergo speech production.
Primary outcome measures
- Mean Change in Neural Activity [Time frame: During inpatient hospitalization, up to 14 days after surgical electrode implantation]
Eligibility criteria
Inclusion criteria
- Undergoing iEEG placement in regions of interest (e.g., in the frontal or temporal cortex) for clinically necessary localization of epileptic foci or language mapping
- Fluent English speakers
- Within the normal range for cognitive, speech-language, and hearing capacity
- Normal or corrected-to-normal visual acuity
Exclusion criteria
- Individuals with intellectual disability
- Lack of fluent English comprehension/production
- Inadequate speech ability for the research tasks.
- History of autism or ADHD
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Basic science
Study locations
United States · 1 center
- UPMC Children's Hospital of Pittsburgh — Pittsburgh
Identifiers
NCT: NCT07713706 · STUDY25040153 · R00DC020235