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NCT04650932Recruiting

Dual Frequency Stimulation in Parkinson's Disease

Dual Frequency, Dual Region Deep Brain Stimulation of the Subthalamic Nucleus in Parkinson's Disease

Source: ClinicalTrials.gov · Last updated 14 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
16 Nov 2020
Start date
22 Oct 2022
Primary completion date
30 Dec 2026
Lead sponsor
University of California, Davis
NCT number
NCT04650932

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 22 Oct 2022 to the primary completion date, 30 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Pregnant women (note: pregnant women are not candidates for DBS surgery), and prisoners

Other

  • 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
  • Non-English speaking individuals. Cognitive tasks will only be conducted in English.

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UC Davis Health
Coordinator of this site? Confirm its status
SacramentoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.