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NCT05558189Not yet recruiting

Vibrotactile Coordinated Reset for the Treatment of Post Surgery Refractory Parkinson's Disease Patients

Source: ClinicalTrials.gov · Last updated 25 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of our study is to evaluate Vibrotactile Coordinated Reset stimulation (vCR) and its effects on refractory post-surgery PD. 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.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
23 Sept 2022
Start date
20 Aug 2025
Primary completion date
21 Nov 2026
Lead sponsor
Stanford University
NCT number
NCT05558189

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 20 Aug 2025 to the primary completion date, 21 Nov 2026
  • 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.

Prior treatment

  • Any current drug or alcohol abuse.
  • 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.

Other illness

  • Any significant neuro-psychiatric problems, including acute confusional state, ongoing psychosis, or suicidal tendencies

Other

  • Pregnancy, breast-feeding or wanting to become pregnant
  • Patient is unable to communicate properly with staff (i.e., severe speech problems)
  • Excessive drooling
  • Sensory abnormalities of the fingertips
  • Deep Brain Stimulation treatment
  • PD symptoms so severe and that the patient is bed-bound

Who the study is looking for

  • Age at the time of enrollment: 35 - 92 years
  • Diagnosis of idiopathic Parkinson's disease
  • Surgical treatment for Parkinson's disease that does not involve Deep Brain Stimulation
  • Fluent in English
  • Appropriate social support if required during an off state.
  • Comfortable with technology; can use a computer, check email, and access the internet; can initiate and engage in a virtual meeting for training and monitoring purposes.
  • Lives in the United States

Age in the registry: 35 years to 92 years · 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
Stanford University
Coordinator of this site? Confirm its status
StanfordUnited StatesUnknown status

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