Aim 3 Particle Swarm Optimization Postural Instability Gait Disorder

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

In Parkinson's disease (PD) patients undergoing standard-of-care Deep Brain Stimulation (DBS) therapy, to compare the effect on Parkinson's symptoms of two different neurostimulator settings designed to differ from each other as much as possible with respect to how much they activate two different neuroanatomical structures: the axonal pathway from Globus Pallidus (GP) to Pedunculopontine Nucleus (PPN), and the axonal pathway from PPN to GP.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Diagnosis of Parkinson's Disease

• Bilateral DBS in STN or GP

• At least 3 months after lead implantation

• Montreal Cognitive Assessment (MoCA):

⁃ MoCA=23+

⁃ OR: If MoCA score is 23 or less, UBACC will be performed to ensure capacity to consent. If UBACC results are unclear, the MacCAT-CR will be performed. Failed or unclear MacCAT-CR results will exclude the study candidate.

• Between 18-85 years of age

• Has undergone pre-operative 7T MRI (as part of protocol #1210M22183 or standard-of-care) and post-operative CT imaging (standard of care).

Locations
United States
Minnesota
University of Minnesota
RECRUITING
Minneapolis
Contact Information
Primary
Johanna Caskey, BA
caske039@umn.edu
763-353-9470
Time Frame
Start Date: 2024-03-19
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 30
Sponsors
Leads: University of Minnesota

This content was sourced from clinicaltrials.gov