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Clinical Trial Summary

This study will enroll people with SCI who have spasticity and some ability to walk. The goal is to understand if standing on a platform and receiving WBV results in decreased spasticity and improved walking ability. Published article is available (PMID: 29959653)


Clinical Trial Description

Phase 1 of this study has been successfully completed. The results of Phase 1 indicate that a single session of WBV lasting for a total of 6 minutes (delivered in eight 45-sec bouts) at a high-frequency (50Hz) was associated with the largest decrease in spasticity (as measured by the pendulum test). The goal for Phase 2 is to determine whether longer doses of WBV result in greater reductions in spasticity as well as improvements in walking ability. Two different doses of WBV, a short dose and a long dose, will be tested. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02340910
Study type Interventional
Source Shepherd Center, Atlanta GA
Contact
Status Completed
Phase N/A
Start date February 2, 2015
Completion date March 6, 2020

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