Vibrotactile Coordinated Reset in Parkinson's Disease - Proof of Concept Study

Trial ID or NCT#

NCT06028477

Status

not recruiting iconNOT RECRUITING

Purpose

The purpose of our study is to evaluate Vibrotactile Coordinated Reset stimulation (vCR) and its effects on Parkinson's symptoms. vCR will be administered with a device called the Stanford Glove. vCR is expected to provide patients with a non-invasive alternative to the most widely used treatments such as Levodopa and/or deep brain stimulation. Patients will be followed for 14 months.

Official Title

Vibrotactile Coordinated Reset in Parkinson's Disease - Proof of Concept Study

Eligibility Criteria

Ages Eligible for Study: 18 Years to 92 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. Ages 18 or older
    1. * Diagnosed with idiopathic Parkinson's Disease* Fluent in English* Off-state UPDRS III motor score at least 30, as assessed within the past 6 months before study consent or at Screening Visit.* Demonstrates understanding of the study requirements and is able and willing to sign the informed consent form and complete study procedures.
Exclusion Criteria:
  1. * Participation in another drug, device, or biologics trial concurrently or within the preceding 30 days. Any other trial participation should be approved by the Principal Investigators.* Pregnancy, breast-feeding or wanting to become pregnant* Physical limitations unrelated to PD that would affect motor ratings* Has implantation of a medical device* Sensory abnormalities of the fingertips
View All Criteria
Show Less

Investigator(s)

Vivek P. Buch, MD
Vivek P. Buch, MD
Neurosurgeon
Assistant Professor of Neurosurgery

Contact us to find out if this trial is right for you.

Contact

Jessica Yankulova
650-474-9547

View on ClinicalTrials.gov