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NOT YET RECRUITING
NCT06290609
NA

Vibrotactile Coordinated Reset for Spasticity After Spinal Cord Injury

Sponsor: Stanford University

View on ClinicalTrials.gov

Summary

The purpose of our study is to evaluate vibrotactile Coordinated Reset (vCR) and its effects on spasticity symptoms in incomplete spinal cord injured patients. vCR will be administered with a device called the Stanford CR Glove. vCR is expected to provide patients with a non-invasive alternative to the most widely used treatments such as oral baclofen and or deep brain stimulation. Patients will be followed for three months and will be asked to come to the lab for clinical testing 4 times during this period. A total of 30 patients will be included in the study.

Official title: Control of Incomplete Spinal Cord Injury-Related Spasticity by Means of Vibrotactile Coordinated Reset Fingertip Stimulation

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-03-15

Completion Date

2028-06-15

Last Updated

2025-05-15

Healthy Volunteers

No

Interventions

DEVICE

Vibrotactile Coordinated Reset

The experimental device, the Stanford CR Glove, is designed to deliver vibratory stimulation to the fingertips of each hand according to a specific pattern, known as vibrotactile Coordinated Reset, which theoretically disrupts abnormal neuronal synchrony and is expected to restore function.

Locations (1)

Stanford University

Stanford, California, United States