Stimulating Brain Areas (VOP/VIM) with Electricity for Movement Disorders
This study is looking for people who are already scheduled to have deep brain stimulation (DBS) surgery for movement disorders, such as essential tremor. The researchers want to understand how stimulating specific brain areas with electricity, called Direct cortical stimulation and deep brain stimulation of motor thalamus, helps improve movement and muscle control. During your standard DBS surgery, a temporary strip electrode will be placed on the surface of your brain to record brain activity and test how the stimulation affects your movement. The study will measure electromyography activity (muscle electrical activity) 14 days after the procedure to see the effects. The study plans to enroll 60 participants, but its current recruitment status is unclear.
- Study design
- This is an interventional study that plans to enroll 60 participants. It involves a specific procedure during your scheduled deep brain stimulation surgery.
- What's involved
- You would undergo deep brain stimulation surgery, during which additional temporary electrodes will be placed to record brain activity and test the effects of stimulation. You will also perform movement and articulation exercises during this time.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your electromyography activity will be measured 14 days after the procedure.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Stimulating Specific Brain Areas (VOP/VIM) With Electricity to Improve Movement and Muscle Control
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Jorge Gonzalez-Martinez, MD, PhD · PRINCIPAL_INVESTIGATOR · University of Pittsburgh
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Electromyography Activity14 days
The investigators will record electromyography activity (EMG) to measure the motor evoked potentials of upper limb and facial muscles. At the end of the procedures these needles and/or the superficial adhesive electrodes will be removed. Based on the preliminary data, the investigators will consider the number of participants with at least an 18% increase in muscle activation as minimally acceptable.