Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
NA
10 participants
INTERVENTIONAL
2025-04-10
2027-07-30
Brief Summary
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Brain-machine interfaces (BMIs) have shown promise in understanding motor functions by decoding brain activity. It is believed that BMIs could provide both accurate indicators of FOG and targeted treatments for it in PD.
Our objectives are to use a high-density ECoG-based BMI to both record and stimulate brain activity during real-world gait and FOG in PD patients who are undergoing standard DBS procedures. Our goals are to improve our understanding of the brain's role in FOG and normal gait in PD and to develop new treatments based on cortical stimulation.
Aim 1 - Identify gait biomarkers: brain activity from the M1/SMA cortex during different phases of walking and during FOG episodes, both with and without medication will be recorded. Machine learning will be used to identify the brain patterns linked to FOG.
Aim 2 - Use cortical stimulation to stop FOG: Cortical stimulation and its effects on leg and trunk movements will be studied by measuring muscle activity, movement, and posture during different states, such as resting, standing, walking, and during FOG episodes. The type of stimulation which is most effective at stopping FOG will be identified.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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ECoG implantation
Patients will be implanted with high-density cortical ECoG arrays during DBS surgery.
Brain Stimulation
Studies will be conducted using ECoG, with a bidirectional interface, both recording (aim/phase 1) and stimulating (aim/phase 2), during real-world gait and FOG in PD patients over the course of 7-days of gait experiments.
Interventions
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Brain Stimulation
Studies will be conducted using ECoG, with a bidirectional interface, both recording (aim/phase 1) and stimulating (aim/phase 2), during real-world gait and FOG in PD patients over the course of 7-days of gait experiments.
Eligibility Criteria
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Inclusion Criteria
* Debilitating FOG in the off-medication condition with only partial response to levodopa (defined as the witnessed occurrence of FOG during the on phase of the pre-DBS L-dopa challenge)
* Clinically established FOG (i.e. reported by patient/caregiver AND seen by the examiner in the clinic)
* Able to provide informed consent, comply with study protocol
Exclusion Criteria
* Previous brain surgery
* Other disorders potentially biasing assessment
* Absence of FOG in the medication on condition (a population already manageable with current standard of treatment).
ALL
No
Sponsors
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University of Toronto
OTHER
Responsible Party
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Alfonso Fasano
Professor
Locations
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Movement Disorders Centre - Toronto Western Hospital
Toronto, Ontario, Canada
Countries
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Other Identifiers
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24-5435
Identifier Type: -
Identifier Source: org_study_id
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