N
← Back to Search
Sponsored

Accelerate Your Clinical Trial Recruitment

Reach thousands of high-intent patients matching your specific inclusion criteria.

Start Campaign
RECRUITING Not applicable ClinicalTrials.gov

Dual Frequency Stimulation in Parkinson's Disease

Sponsor: University of California, Davis • ClinicalTrials.gov ID: NCT04650932

Registry updated: 2026-09-14
Ad

Recruiting for Similar Conditions?

Sponsors are looking for patients like you. See if you qualify for compensated research studies.

Check Eligibility →

Description

Deep brain stimulation (DBS) in the dorsal region of the subthalamic nucleus (STN) is very effective for reducing motor symptoms of Parkinson's disease (PD). Modeling studies suggest that this therapy may result in current spread into the ventral STN, causing altered cognitive processes. As a result, current stimulation parameters often lead to worsening in verbal fluency, executive function, and, particularly, cognitive control. There is evidence suggesting that low frequency oscillatory activity occurs across brain circuits important in integrating information for cognition. Preclinical studies and human recording studies indicate these low frequency theta oscillations drive cognitive control during cognitive tasks. Thus, the purpose of this study is to determine the safety, tolerability, and efficacy of low frequency stimulation (LFS) of the ventral STN alongside standard high frequency stimulation (HFS) of the dorsal STN in patients with PD.

Interventions

  • Deep brain stimulation (Device)
    Patients with idiopathic Parkinson's disease who have previously been implanted with the Boston Scientific VerciseTM DBS system for at least 3 months. These patients will already be receiving high-frequency dorsal STN stimulation as part of the standard of care for PD. Once patients have provided consent and are enrolled in this study, they will receive simultaneous low-frequency stimulation of the ventral STN to examine if there are any effects on cognitive performance.

Eligibility criteria

Inclusion Criteria: * Individuals who are 18 years and older * Individuals with idiopathic Parkinson's Disease who previously underwent implantation with the Boston Scientific VerciseTM DBS system * Individuals who have been implanted with the Boston Scientific VerciseTM DBS system for at least 3 months * Individuals diagnosed with advanced PD who had bilateral dorsal subthalamic nucleus DBS surgery, as standard of care for motor improvement, with distal contacts of the electrodes implanted into the ventral STN Exclusion Criteria: * Individuals unable to provide consent and/or lack capacity to consent * Individuals diagnosed with any cognitive or physical impairments that would limit their ability to participate in the cognitive testing * Individuals who score below 15 on the Montreal Cognitive Assessment Test-Blind * Individuals who score above 20 on the Center for Epidemiologic Studies Depression Scale * Pregnant women (note: pregnant women are not candidates for DBS surgery), and prisoners * Non-English speaking individuals. Cognitive tasks will only be conducted in English.

Conditions

Parkinson Disease

Locations

  • UC Davis Health — Sacramento, California, United States
Sponsored

Partner with Nurenyx

Showcase your study to thousands of motivated patients matching your criteria.

Learn More

Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record