Actively Recruiting
Basal Ganglia Contributions to Transitions in Freezing of Gait and Parkinsons Disease
Led by University of Minnesota · Updated on 2026-03-03
36
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
Sponsors
U
University of Minnesota
Lead Sponsor
N
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research investigates the causes and signs of freezing of gait FOG in people with Parkinsons disease PD. It focuses on understanding the underlying brain activity and biomarkers associated with FOG and how cues may improve movement. The study uses the Medtronic Percept22 deep brain stimulation DBS system, a device approved by the FDA, to measure local field potentials LFPs in individuals with PD, both with and without FOG, through three separate experiments. Participants will be grouped based on their PD diagnosis and whether they experience FOG. The study compares brain activity during different movement tasks gait initiation with and without cues, movement transitions versus freezing events during a provocation course, and rapid alternating wrist or foot movements. Participants will have their Parkinsons medications withheld for 12 to 24 hours before testing and their DBS device turned off at the start of visits. During the study visits, researchers will assess various movement and brain activity measures, including magnitude and duration of anticipatory postural adjustments, step characteristics, coherence between brain areas and muscles, number of freezing episodes, and rapid alternating movements. These measurements help understand how brain signals relate to movement issues in PD. Participants must be able to walk independently and have an implanted Medtronic Percept DBS device. The study includes safety monitoring and consent capacity assessments throughout participation.
CONDITIONS
Brief Title
Percept Transitions in FOG and PD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of idiopathic Parkinson's disease (PD).
- Age between 21 and 75 years.
- Ability to walk independently without assistive devices for at least 50 meters.
- Implanted Medtronic Percept deep brain stimulation device.
- At least 3 months since initial activation of the neurostimulator.
- Inclusion of undervalued, under-represented, or disenfranchised social groups.
- Inclusion of active military members and Department of Defense personnel.
- Inclusion of individuals or groups disadvantaged in income, housing, or healthcare distribution.
You will not qualify if you...
- Diagnosis of dementia with Lewy bodies, Multiple Systems Atrophy, Alzheimer's disease, or other neurodegenerative disorders besides Parkinson's.
- History of seizures or significant neurological disorders affecting study participation.
- History of musculoskeletal disorders significantly impacting walking or limb movement related to experimental tasks.
- History of muscular conditions of the neck and back, including whiplash, affecting walking experiments.
- History of visual or vestibular conditions affecting participation.
- Reduced capacity to consent as assessed by specific cognitive tests.
- Pregnancy.
- Post-operative complications or adverse effects impacting safety or study results.
Research Team
M
Madison Aasen, MS
S
Sommer Amundsen-Huffmaster, PhD
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