Fact CheckerSign in

NCT05490277Not yet recruiting

Vibrotactile Coordinated Reset for the Treatment of Chronic Stroke

Source: ClinicalTrials.gov · Last updated 15 May 2025 · 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 motor ability within stroke patients. vCR will be administered with a device called the Vibrotactile (VT) Brain Glove. vCR is expected to provide patients with a non-invasive therapy to aid in recovery from a stroke. This study will include a dedicated sham arm that will aid in understanding true treatment effects from vCR.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
2 Aug 2022
Start date
Jan 2026
Primary completion date
Nov 2028
Lead sponsor
Stanford University
Diseases
Stroke
NCT number
NCT05490277

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From Jan 2026 to the primary completion date, Nov 2028
  • 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 biologic trial concurrently or within the preceding days
  • Botox, baclofen or any other treatment for spasticity except for bracing or splinting within the previous 3 months

Other illness

  • Any significant psychiatric problems, including acute confusional state (delirium), ongoing psychosis, or clinically significant depression
  • History of recurrent or unprovoked seizures
  • Any neurological disorder treatments that involve intracranial surgery or device implantation
  • History or presence of other major neurological or orthopedic diseases other than stroke that limits motor functioning or cognitive ability

Other

  • Pregnancy, breastfeeding or wanting to become pregnant during the trial
  • More than 5 degrees of contracture at shoulder, elbow, wrist, finger, hip, knee, or ankle
  • Must be able to communicate with staff
  • Severe sensory abnormalities of the fingers such as vibratory urticaria

Who the study is looking for

  • Age at the time of enrollment: 18-80 years
  • Diagnosis of ischemic or hemorrhagic stroke
  • Disease period of more than 6 months
  • Mini Mental State Examination of at least 24 points
  • No medications that affect balance
  • Motor deficit
  • Use of Motricity Arm and Leg index to include impaired individuals with some functioning
  • Modified Rankin Scale for Neurologic Disability: Scores 3 or 4

Age in the registry: 18 years to 80 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.