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Vibrotactile Stimulation for Parkinson's Disease

N/A
Waitlist Available
Research Sponsored by Stanford University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Feels comfortable going off PD related medication during in person study visits
Idiopathic Parkinson's Symptoms between hoehn and yahr stage 1
Must not have
Brain surgery
Patient is unable to communicate properly with staff (i.e., severe speech problems)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 6 months, 12 months, 18 months, 24 months
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing a new treatment called Vibrotactile Coordinated Reset stimulation (vCR) for people with early stage Parkinson's disease. The treatment uses a device called the Stanford Glove to send vibrations to the nervous system. It aims to provide a non-invasive alternative to common treatments like medication or surgery by helping the brain's nerve cells work better.

Who is the study for?
This trial is for English-speaking adults aged 35-90 in the U.S. with early stage Parkinson's (Hoehn and Yahr stage 1). Participants must be comfortable stopping their Parkinson's medication during visits, able to use technology for virtual meetings, and have social support if needed.
What is being tested?
The study tests Vibrotactile Coordinated Reset (vCR) using a device called vibrotactile axon Glove on early-stage Parkinson's symptoms. It offers a non-invasive treatment alternative, monitoring patients over two years.
What are the potential side effects?
Since vCR is non-invasive and doesn't involve drugs or surgery, side effects are minimal but may include discomfort at the glove contact points or skin irritation from prolonged use.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am okay with stopping my Parkinson's disease medication for study visits.
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My Parkinson's is in the early stage (stage 1).
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I am between 35 and 90 years old.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have had brain surgery.
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I have severe difficulty speaking or communicating.
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I experience excessive drooling.
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I feel unusual sensations in my fingertips.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 6 months, 12 months, 18 months, 24 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 6 months, 12 months, 18 months, 24 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Movement Disorders Society Unified Parkinson's Disease Rating Scale Part 3 (MDS-UPDRS III) off medication
Secondary study objectives
Freezing of gait questionnaire (FOG)
Movement disorders unified Parkinson's rating scale (MDS-UPDRS) part 1
Movement disorders unified Parkinson's rating scale (MDS-UPDRS) part 2
+8 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Vibrotactile Coordinated Reset (vCR)Experimental Treatment1 Intervention
Vibrotactile Coordinated Reset delivers vibratory stimulation to the fingertips of each hand. A specific pattern of vibration to each fingertip is delivered which theoretically disrupts abnormal synchrony in the brain.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Parkinson's Disease (PD) include medications like levodopa, which replenishes dopamine levels in the brain, and deep brain stimulation (DBS), which modulates neural activity through electrical impulses. These treatments aim to alleviate motor symptoms by addressing the dopamine deficiency and abnormal neural activity characteristic of PD. Non-invasive neuromodulation techniques, such as Vibrotactile Coordinated Reset (vCR), use patterned vibratory stimuli to reset abnormal neural oscillations without surgery. This approach is significant for PD patients as it offers a potentially safer and more accessible alternative to invasive treatments, aiming to improve motor function and quality of life.
Essential tremor amplitude modulation by median nerve stimulation.Coordinated reset neuromodulation for Parkinson's disease: proof-of-concept study.

Find a Location

Who is running the clinical trial?

Stanford UniversityLead Sponsor
2,467 Previous Clinical Trials
17,496,082 Total Patients Enrolled

Media Library

Vibrotactile Coordinated Reset (Other) Clinical Trial Eligibility Overview. Trial Name: NCT05545826 — N/A
Parkinson's Disease Research Study Groups: Vibrotactile Coordinated Reset (vCR)
Parkinson's Disease Clinical Trial 2023: Vibrotactile Coordinated Reset Highlights & Side Effects. Trial Name: NCT05545826 — N/A
Vibrotactile Coordinated Reset (Other) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05545826 — N/A
Parkinson's Disease Patient Testimony for trial: Trial Name: NCT05545826 — N/A
~13 spots leftby Oct 2027