Effects of Whole Body Vibration in Elderly Patients Requiring Rehabilitation: A Pilot Study
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Purpose
The aim of this study is to accumulate data about the influence of whole body vibration on the functional recovery of adult patients with various neuromuscular and musculoskeletal deficits requiring physical medicine and rehabilitation treatments.
| Condition | Intervention |
|---|---|
|
Neuromuscular Deficits Musculoskeletal Deficits |
Device: whole body vibration using a Galileo vibrating platform |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Effects of Whole Body Vibration in Elderly Patients Requiring Rehabilitation: A Pilot Study |
- Berg Balance Test [ Time Frame: begining and end of intervention ] [ Designated as safety issue: No ]
- Sit to stand test [ Time Frame: begining and end of intervention ] [ Designated as safety issue: No ]
- timed walking test [ Time Frame: begining and end of intervention ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 300 |
| Study Start Date: | October 2001 |
| Study Completion Date: | December 2009 |
| Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: I
Subjects who receive whole body vibration
|
Device: whole body vibration using a Galileo vibrating platform
whole body vibration at 20 hertz for 3 minutes 3 to 5 days per week for up to 12 weeks
|
|
No Intervention: N
Subjects do not receive whole body vibration intervention
|
Detailed Description:
We know that whole body vibration can cause remarkable increase in power in athletes, however, to what extent elderly and disabled individuals could benefit from it is currently unknown. Our primary goal is to investigate if treatment with whole body vibration in elderly persons and patients with various neuromuscular and musculoskeletal deficits would result in more rapid return of their function and presumably at a higher level than comparable group of patients undergoing standard physical therapy.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- A history of one of the following conditions: CVA, Parkinson's disease, incomplete spinal cord injury, frail elderly, urinary incontinence, COPD, fibromyalgia
- Patients with neuromusculoskeletal problems affecting strength, balance, and coordination
- Must have all appendages (arms and legs) intact, not an amputee
Exclusion Criteria:
- Pregnancy
- Unable o participate in continuing outpatient therapy services at a location where the whole body vibration equipment is available
- Untreated deep venous thrombosis
- Other condition that will lead to poor treatment adherence
- History of join replacement of lower limbs, shoulders, or devices in the spine
Contacts and Locations| United States, Ohio | |
| The Ohio State University | |
| Columbus, Ohio, United States, 43210 | |
| Principal Investigator: | Velimir Matkovic, M.D., Ph.D. | Ohio State University |
More Information
No publications provided
| Responsible Party: | Velimir Matkovic, M.D., Ph.D. Professor, The Ohio State University |
| ClinicalTrials.gov Identifier: | NCT00610298 History of Changes |
| Other Study ID Numbers: | 2001H0215 |
| Study First Received: | December 26, 2007 |
| Last Updated: | July 22, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Ohio State University:
|
disability affecting strength, balance and coordination |
ClinicalTrials.gov processed this record on May 19, 2013