Vibrotactile Coordinated Reset for Parkinson's Patients of a More Variable Population

Part of paid clinical trials in Stanford, California.

Sponsor
Stanford University
Study ID
NCT06029686
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
35 Years - 100 Years
Healthy Volunteers
Not accepted

Interventions

  • Stanford Glove — DEVICE
    The vibrotactile device sends weak non-painful pattern type vibratory stimulus to the fingertips and is non-invasive. Some patient may experience dyskinesia which can me medicated with a decrease in Parkinson's medication

Study Details

The purpose of our study is to evaluate Vibrotactile Coordinated Reset stimulation (vCR) and its effects on Parkinson's symptoms of a more variable population. 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 two years.

Key Dates

Start date
May 31, 2025
Status verified
Aug 2024
Primary completion
Dec 31, 2026
Completion
Jan 31, 2027

Study Design

Enrollment
20 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Stimulation
    Patients will be asked to stimulate using a non invasive vibrotactile device.

Primary Outcome Measure

Change in Parkinsonian symptoms as defined by the change in Movement Disorder Society Unified Parkinson's Disease Rating Scale Part III Score [ Time Frame: 6 months ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Stanford UniversityStanfordCalifornia94305-

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