The Effect of Whole Body Vibration on Spasticity in Persons With Spinal Cord Injury
Status: | Recruiting |
---|---|
Conditions: | Hospital, Hospital, Neurology, Orthopedic |
Therapuetic Areas: | Neurology, Orthopedics / Podiatry, Other |
Healthy: | No |
Age Range: | 18 - 70 |
Updated: | 4/2/2016 |
Start Date: | April 2014 |
Contact: | Trevor A. Dyson-Hudson, M.D. |
Email: | tdysonhudson@kesslerfoundation.org |
Phone: | 973-324-3576 |
The Effect of Whole Body Vibration on Spasticity in Spinal Cord Injury Patients
Extended periods of tilt table standing have been observed to improve spasticity in
individuals with spinal cord injury (SCI). The purpose of this study is to determine the
effect of three sessions of whole body vibration while tilt table standing on spasticity in
individuals with a complete or incomplete SCI above the neurological level of T10.
Participants in this study will undergo whole body vibration while standing on a tilt table
for a total of approximately 14 minutes for a total of 3 sessions on 3 separate days.
Spasticity monitoring will be evaluated prior to and after the intervention with the
Modified Penn Spasm Frequency Scale, an interview to obtain the individual's perception and
impression of the effect of whole body vibration on the performance of activities of daily
living, quality of life, pain scale, and global impression of change.
individuals with spinal cord injury (SCI). The purpose of this study is to determine the
effect of three sessions of whole body vibration while tilt table standing on spasticity in
individuals with a complete or incomplete SCI above the neurological level of T10.
Participants in this study will undergo whole body vibration while standing on a tilt table
for a total of approximately 14 minutes for a total of 3 sessions on 3 separate days.
Spasticity monitoring will be evaluated prior to and after the intervention with the
Modified Penn Spasm Frequency Scale, an interview to obtain the individual's perception and
impression of the effect of whole body vibration on the performance of activities of daily
living, quality of life, pain scale, and global impression of change.
Inclusion Criteria:
- The subject is male or female, 18 to 70 years of age, inclusive.
- The subject has neurological impairment secondary to a spinal cord injury that
occurred at least six (6) months prior to the study that can be categorized as either
a complete or incomplete spinal cord injury.
- The neurological level of lesion is above T10.
- The subject has self-reported stable moderate to severe spasticity (Modified Ashworth
Score scale at or greater than a 2 at the hips or knees). Patients can be enrolled if
on a stable dose of oral medications or intrathecal medications.
- The subject has self reported spasticity that negatively impacts his or her quality
of life, impairs ability to perform activities of daily living (such as transfers,
sitting, sleep, wheelchair use, and hobbies).
- The subject is able to stand with the assistance of a tilt table at a minimum of 70
degrees for 45 minutes without significant orthostasis or other adverse events or
symptoms.
- The subject is able and willing to comply with the protocol.
- The subject is able to and has voluntarily given informed consent prior to the
performance of any study-specific procedures.
Exclusion Criteria:
- The subject does not self report lower limb spasticity.
- The subject does not have self reported spasticity that negatively impacts his or her
quality of life, impairs ability to perform activities of daily living (such as
transfers, sitting, sleep, wheelchair use, and hobbies).
- The subject experiences symptoms consistent with infection, including but not limited
to fever, chills, dysuria, gallbladder or kidney stones.
- The subject experiences pain that is not well controlled with consistent pain
medication use.
- The subject has recent thromboembolism, diabetes mellitus, intractable hypertension
or cardiac/pulmonary instability, internal fixation implants, acute thrombosis,
pregnancy, acute inflammation of the locomotor system including active arthrosis or
arthropathy, acute tendinopathy, acute hernia, acute discopathy, recent post-surgical
wounds, epilepsy, rheumatoid arthritis, or recent fractures<6 months.
- The subject has a lumbar spinal hardware or artificial joints in the lower
extremities.
- The subject is participating in any experimental studies that could alter the
patient's spasticity.
- The subject has a concomitant brain injury or other cognitive deficits that would
preclude following instructions.
- The subject has skin breakdown in areas receiving direct pressure during tilt table
standing.
- The subject has any medical condition, including psychiatric disease that would
interfere with the interpretation of the study results or the conduct of the study.
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