Vibrotactile Coordinated Reset for Spasticity After Spinal Cord Injury

Status Not yet recruiting

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06290609
Study type	Interventional
Source	Stanford University
Contact	Jessica Yankulova
Phone	650-474-9547
Email	jessky@stanford.edu
Status	Not yet recruiting
Phase	N/A
Start date	March 15, 2024
Completion date	June 15, 2024

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