Whole-body Vibration as a Treatment for Parkinson's Disease
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ClinicalTrials.gov Identifier: NCT02306863 |
Recruitment Status : Unknown
Verified February 2015 by Adam Koebel, Sun Life Financial Movement Disorders Research and Rehabilitation Centre.
Recruitment status was: Recruiting
First Posted : December 3, 2014
Last Update Posted : February 16, 2015
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Condition or disease | Intervention/treatment | Phase |
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Idiopathic Parkinson's Disease Primary Parkinsonism | Device: vibrating chair Device: sham treatment | Not Applicable |
Parkinson's disease (PD) is a progressive neurodegenerative disease resulting in the loss of dopaminergic neurons projecting from the substantia nigra pars compacta to the striatum.
Whole-body vibration (WBV) is potentially beneficial in treating Parkinson's disease because it has been shown to elicit effects specific to both the brain and muscular system. Animal models of PD indicate that whole-body vibration can increase striatal dopamine levels, as well as the number of dopaminergic neurons in the substantia nigra. These findings were correlated with increased levels of brain-derived neurotrophic factor.
In addition to the potentially neuroplastic effects, >20 Hz WBV has been shown to improve muscular performance. Improved muscular performance is believed to be attributed to WBV induced neuromuscular effects rather than muscle hypertrophy, with the specific mechanism defined as the tonic vibration reflex.
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 60 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double (Participant, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | The Efficacy of Long-term Whole-body Vibration in the Treatment of Parkinson's Disease |
Study Start Date : | January 2015 |
Estimated Primary Completion Date : | July 2015 |
Estimated Study Completion Date : | August 2015 |

Arm | Intervention/treatment |
---|---|
Experimental: whole-body vibration
40 Hz Whole-body vibration applied via physioaccoustic method for 12 weeks, 3 times a week
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Device: vibrating chair
vibration provided via physioacoustic method |
Sham Comparator: sham treatment
simulated whole-body vibration applied 3 times a week for 12 weeks
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Device: sham treatment
simulated whole-body vibration
Other Name: placebo |
- Unified Parkinson's Disease Rating Scale (UPDRS) section III [ Time Frame: change from baseline, 12 weeks, and 2 week washout ]clinician monitored motor evaluation
- Gait Assessment [ Time Frame: change from baseline, 12 weeks, and 2 week washout ]pressure sensitive carpet (GAITRite) measuring gait parameters (step length, step velocity, stride-to-stride variability, etc)
- Timed Up & Go (TUG) Test [ Time Frame: change from baseline, 12 weeks, and 2 week washout ]measuring time participants take to stand up from chair, walk towards an obstacle, turn around, walk back to chair, and sit back down again
- Timed Grooved Pegboard Task [ Time Frame: change from baseline, 12 weeks, and 2 week washout ]25 pegs with a key along one side must be rotated to properly be inserted into slot on board (measuring time-in and time-out)

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Diagnosed with idiopathic Parkinson's Disease by a Neurologist
- Currently taking anti-Parkinsonian medication
- Able to stand for 2 minutes without assistance
- Able to walk 10 meters without assistance
- Ability to understand English instructions
- Normal or corrected vision
Exclusion Criteria:
- A neurological disease other than PD
- recent stroke
- cardiovascular disease
- previous major hemorrhage
- artificial pacemaker
- currently pregnant
- Current participation in any physical therapy or experimental treatments
- Peripheral neuropathy, severe osteoporosis
- Visual impairments that cannot be corrected
- Clinically diagnosed with dementia
- Greater than mild dementia (screened using Montreal Cognitive Assessment (MOCA) <24 being excluded)

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02306863
Contact: Adam K Koebel, BSc | 519-884-0710 ext 3924 | koeb2420@mylaurier.ca | |
Contact: Patricia Freeman | 519-884-0710 ext 2877 | pafreeman@wlu.ca |
Canada, Ontario | |
Sun Life Financial Movement Disorders Research & Rehabilitation Centre | Recruiting |
Waterloo, Ontario, Canada, N2L 3J5 | |
Contact: Patricia Freeman 519-884-0710 ext 3924 pafreeman@wlu.ca | |
Contact: Adam Koebel 519-884-0710 koeb2420@mylaurier.ca | |
Principal Investigator: Adam Koebel |
Principal Investigator: | Adam K Koebel, BSc | Wilfrid Laurier University |
Responsible Party: | Adam Koebel, Undergraduate Thesis Student, Sun Life Financial Movement Disorders Research and Rehabilitation Centre |
ClinicalTrials.gov Identifier: | NCT02306863 |
Other Study ID Numbers: |
4291 |
First Posted: | December 3, 2014 Key Record Dates |
Last Update Posted: | February 16, 2015 |
Last Verified: | February 2015 |
Parkinson's Disease whole-body vibration WBV |
Parkinson Disease Parkinsonian Disorders Basal Ganglia Diseases Brain Diseases Central Nervous System Diseases |
Nervous System Diseases Movement Disorders Synucleinopathies Neurodegenerative Diseases |