Dose-Response Effects of Whole Body Vibration on Spasticity and Walking in SCI



Status:Recruiting
Conditions:Hospital, Orthopedic
Therapuetic Areas:Orthopedics / Podiatry, Other
Healthy:No
Age Range:16 - 72
Updated:8/19/2018
Start Date:January 2015
End Date:August 2020
Contact:Edelle Field-Fote, PT, PhD
Email:Edelle_Field-Fote@Shepherd.org
Phone:404-603-4274

Use our guide to learn which trials are right for you!

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)

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.

Inclusion Criteria:

- have spinal cord injury of at least 6 months duration.

- be between the ages of 16 - 72 years old.

- be able to sit at the edge of the mat without the assistance of another person.

- be able to tolerate standing.

- have at least mild spasticity affecting the lower extremity muscles.

- be able to understand and provide own consent

- You may participate if you use prescription medications, including baclofen pump for
control of spasticity, as the dosage is stable.

- obtain medical clearance for standing if you have been injured more than 1 year and
are not regularly walking or standing.

Exclusion Criteria:

- progressive or potentially progressive spinal lesions, including degenerative, or
progressive vascular disorders of the spine and/or spinal cord.

- neurologic level below spinal level T12

- history of cardiovascular irregularities

- problems following instructions

- orthopedic problems that would limit your participation in the protocol (e.g. knee or
hip flexion contractures of greater than 10 degrees).
We found this trial at
1
site
Atlanta, Georgia 30309
Phone: (404) 603-4274
?
mi
from
Atlanta, GA
Click here to add this to my saved trials