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Speech Production Tasks for Understanding Speech Disorders
N/A
Waitlist Available
Led By Lingyun Zhao, PhD
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up during inpatient hospitalization, up to 14 days after surgical electrode implantation
Awards & highlights
Study Summary
This trial seeks to understand how the brain controls the stopping of speech production, to help us understand communication disorders like stuttering & aphasia.
Who is the study for?
This trial is for individuals with medication-resistant epilepsy at UCSF who are undergoing surgical electrode implantation to locate their seizure focus. They must be willing and able to cooperate with study tasks involving speech production.Check my eligibility
What is being tested?
The study aims to understand how the brain stops ongoing speech, which is crucial for smooth conversations and turn-taking. It will explore neural mechanisms in patients performing speech tasks during electrode monitoring.See study design
What are the potential side effects?
Since this trial involves non-invasive speech production tasks, there are no direct side effects from interventions like drugs or surgery. However, participants may experience fatigue or stress from the tasks.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ during inpatient hospitalization, up to 14 days after surgical electrode implantation
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~during inpatient hospitalization, up to 14 days after surgical electrode implantation
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Mean Change in Neural Activity
Secondary outcome measures
Number of sites with stimulation induced speech termination
Trial Design
1Treatment groups
Experimental Treatment
Group I: Voice and Electrocorticography (ECoG) recording during Speech Production TasksExperimental Treatment1 Intervention
Participants produce speech following visual cues on a computer while ECoG signals for neural activity and voice was recorded during their inpatient hospitalization at the University of California, San Francisco (UCSF).
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Who is running the clinical trial?
University of California, San FranciscoLead Sponsor
2,517 Previous Clinical Trials
15,240,999 Total Patients Enrolled
15 Trials studying Epilepsy
6,086 Patients Enrolled for Epilepsy
National Institute on Deafness and Other Communication Disorders (NIDCD)NIH
331 Previous Clinical Trials
178,457 Total Patients Enrolled
3 Trials studying Epilepsy
109 Patients Enrolled for Epilepsy
Lingyun Zhao, PhDPrincipal InvestigatorUniversity of California, San Francisco
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I have implants for monitoring and can follow study instructions.I am unable to make my own medical decisions.I do not agree to give informed consent for the trial.I have epilepsy that doesn't respond to medication and am getting surgery at UCSF to locate my seizure focus.I am able to understand and complete study tasks despite any cognitive issues.
Research Study Groups:
This trial has the following groups:- Group 1: Voice and Electrocorticography (ECoG) recording during Speech Production Tasks
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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