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NCT07835308RecruitingEarly phase 1

Bayesian Optimization of DBS for Gait

Source: ClinicalTrials.gov · Last updated 28 Sept 2026

Brief summary (registry, in English)

This project aims to establish the feasibility of Bayesian optimization for tuning deep brain stimulation (DBS) to treat gait symptoms in Parkinson's disease (PD) patients. Our primary question is: Can Bayesian optimization of DBS achieve reproducible results within a feasible number of gait measurements? PD patients will be enrolled who have DBS of the subthalamic nucleus (STN) or globus pallidus (GP) in whom at least 3 months have passed since activation of their neurostimulators, for stabilization of clinical stimulator settings. We will apply Bayesian optimization to derive DBS settings which maximally lengthen step length relative to the OFF DBS state.

Status (registry)
Recruiting
Phase (registry)
Early phase 1
Study type
Interventional
Enrollment
15 (estimated)
First submitted
26 Aug 2026
Start date
Dec 2026
Primary completion date
Mar 2031
Lead sponsor
University of Minnesota
NCT number
NCT07835308

What you commit to

  • Study type: Interventional · Early phase 1
  • Planned participants: 15
  • From Dec 2026 to the primary completion date, Mar 2031
  • 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.

Other illness

  • Inability to walk in the off-med, off-stimulation condition (even with safety harness)
  • Gait impaired significantly by a condition other than PD, as determined by the PI

Other

  • Breaks or shorts in active contacts
  • IPG battery nearing end of life (in patients with primary-cell IPGs)
  • Females who are nursing or pregnant
  • Diminished capacity to consent (concluded via UBACC)

Who the study is looking for

  • Diagnosis of Parkinson's Disease
  • DBS in STN or GP (bilateral or unilateral)
  • At least 3 months after lead implantation

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
University of Minnesota
Coordinator of this site? Confirm its status
MinneapolisUnited StatesRecruiting

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