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N/A N=15 Basic Science

The Impact of Exercise on Subthalamic Nucleus Neural Activity in Parkinson's Disease

Parkinson Disease · Deep Brain Stimulation

Enrolled (actual)
15
Serious AEs
0.0%
Results posted
Dec 2025
Primary outcome: Primary: Finger Tapping — 3; 3; 3; 3 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Forced and Voluntary Exercise (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Jay Alberts
Primary completion
Sep 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Finger Tapping
3; 3; 3; 3; 3
PRIMARY
Force Tracking
43.3; 44.9; 41.5; 43.0; 41.9
PRIMARY
Local Field Potential
100.0; 100.0; 131.0; 120.5; 100.0; 100.0

Summary

Fifteen PwPD who have undergone DBS surgery and utilize the Percept system will complete a FE and VE exercise session on a stationary cycle while Off antiparkinsonian medication. Bilateral neural activity of the STN will be continuously recorded for 130 minutes (pre-, during FE or VE and post-exercise). The Movement Disorders Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) III Motor Exam and upper extremity force-tracking task will be used to determine motor response to exercise.

Eligibility Criteria

Inclusion Criteria

  • Adult with a diagnosis of PD by a movement disorders neurologist
  • Previous placement, at least six months, of bilateral Medtronic Precept DBS as standard of care treatment for their PD.
  • Stable and clinically optimized DBS parameters for three months prior to enrollment.
  • Demonstrate the ability to safely mount and dismount a recumbent exercise cycle with an upright back.
  • Willingness to withhold antiparkinsonian medication and DBS stimulation.
  • Exercise clearance using the American College of Sports Medicine (ACSM) Pre-participation Health Screen: a. If the ACSM screen recommends medical clearance, the subject must obtain medical clearance by their health care provider prior to participation; b. Those who choose not to obtain physician clearance will not be eligible for participation.

Exclusion Criteria

  • Diagnosis of dementia or any neurocognitive impairment that compromises the ability to provide informed consent.
  • A musculoskeletal issue that limits one's ability to cycle
  • Neurological disease other than Parkinson's disease (i.e. multiple sclerosis, stroke) that impacts motor or cognitive function
  • Uncontrolled cardiovascular risk factor such as a current cardiac arrhythmia, uncontrolled hypertension, untreated deep vein thrombosis, etc.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05905302). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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