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Recruiting NCT04286308

Cortical-Basal Ganglia Speech Networks

No phase Interventional Parkinson Disease Essential Tremor Dystonia

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: electrophysiological data collection.
Who it may be relevant to
Registry conditions: Parkinson Disease, Essential Tremor, Dystonia. Basic parameters: 18 years — 85 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 →

Overview

In this research study the researchers want to learn more about brain activity related to speech perception and production.

Detailed description

Speech production is disrupted in a number of neurological diseases that involve the basal ganglia, including Parkinson's disease (PD) and dystonia. The investigators will use a novel experimental approach and combination of analytic techniques to elucidate the contribution of neural activity in cortical-basal ganglia circuits to the hierarchical control of speech production, in subjects undergoing deep brain stimulation surgery.

Interventions

  • Other electrophysiological data collection
    Electrophysiological data collection at the time of DBS surgery.

Primary outcome measures

  • The number of subjects providing the interpretable speech related electrophysiological data collection. [Time frame: Duration of single DBS surgery]

Eligibility criteria

Inclusion criteria

  • Subjects scheduled for DBS implantation, as determined by the clinical multidisciplinary movement disorders board with definitive diagnosis of Parkinson's disease, essential tremor or dystonia.
  • Subjects able to provide informed consent and comply with task instructions.
  • Subjects 18-85 years old

Exclusion criteria

  • Subjects with reported hearing loss.
  • Non-English-speaking subjects

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
  • Massachusetts General Hospital — Boston

Identifiers

NCT: NCT04286308 · 2019P003841

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗