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CompletedNCT03777501Updated Jan 23, 2020

The Effect of Whole Body Vibration in Individuals With Parkinson's Disease

An interventional study of non-random whole body vibration and occupational therapy in Parkinson Disease, sponsored by Chang Gung University. Completed at 1 site in Taiwan. Open to participants aged 50 Years to 65 Years. Per ClinicalTrials.gov, last updated 2020-01-23.

Sponsored by Chang Gung University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
50 Years to 65 Years
Sex
All
01

Study summary

Previous studies reported that whole body vibration has the potential impact on balance and walking abilities in individuals with Parkinson's disease; however, the inconsistent treatment protocols and different experimental designs lead to inconclusive results. Therefore, the purpose of this study is to investigate the short term and long term effect of whole body vibration on sensorimotor function in individuals with Parkinson's disease. The experimental design will be randomized double-blinded controlled trial. Sixty individuals with idiopathic Parkinson's disease will be randomly assigned to two groups and they are non-random whole body vibration group and conventional therapy group. Each participant will receive the treatment about one hour after the administration of medicine. For non-random whole body vibration group, participants will be required to maintain the erect standing position on the vibratory platform and the frequency and amplitude of vibratory stimuli will be 6Hz and 3mm respectively. Each treatment includes five sessions and each session is composed of one minute whole body vibration and one minute rest. For the conventional therapy group, participants will receive the occupational therapy including dynamic balance training and functional ambulatory training. Each session is 10 minutes in both groups and all participants will receive one and twelve treatment sessions for short-term and long-term effect respectively. Outcome measures include proprioceptive sensitivity threshold of upper limb, position sense test of the knee joint, Unified Parkinson's disease rating scale-motor (UPDRS motor), functional reach, and time up and go test (TUG). Specifically, the investigators want to answer the following four questions: 1) Is there any difference in proprioceptive sensitivity, motor performance and balance before and after treatment in individuals with Parkinson's disease? 2) Is there any difference in short-term and long term effect of whole body vibration in individuals with Parkinson's disease? 3) Is there any difference in treatment effect in individuals with Parkinson's disease in Taiwan?

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Conditions studied

  • Parkinson Disease

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Keywords

  • proprioception
  • vibration
  • balance
03

In context

Parkinson Disease

4,487 studies on the registry are indexed under Parkinson Disease; 1,082 are open to participants now.

This study's enrollment of 34 is below the median of 40 across 3,294 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

Chang Gung University is the lead sponsor of 63 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • agree to sign the informed consent form.
  • diagnosed with idiopathic Parkinson's disease with Hoehn and Yahr stage 2\~3
  • cognitive impairment (Mini-Mental State Examination [MMSE] score greater than 24 points
  • no depression as evaluated by the Beck Depression Inventory
  • no severe arm injuries or shoulder dislocation which might interfere with proprioceptive function
  • can perform reaching movement
  • no diagnosed peripheral nerve disorders or other neurologic conditions
  • no severe tremor which might interfere with the measurement proprioceptive function

Exclusion criteria

Exclusion Criteria:

  • diagnosed with other central nervous system diseases, ex: stroke
  • had surgeries in head or arms
  • unable to sit for assessment
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
34 participants (actual)

Study arms

  • Experimental
    non-random whole body vibration group

    Each participant will receive the non-random type whole body vibration treatment about one hour after the administration of medicine.

    Behavioral: non-random whole body vibration

  • Active comparator
    conventional therapy group

    For the conventional therapy group, participants will receive the occupational therapy including dynamic balance training and functional ambulatory training. Each session is 10 minutes.

    Behavioral: occupational therapy

Interventions

  • Behavioralnon-random whole body vibration

    Each participant will receive the treatment about one hour after the administration of medicine. For non-random whole body vibration group, participants will be required to maintain the erect standing position on the vibratory platform and the frequency and amplitude of vibratory stimuli will be 6Hz and 3mm respectively. Each treatment includes five sessions and each session is composed of one minute whole body vibration and one minute rest.

  • Behavioraloccupational therapy

    Participants will receive the occupational therapy including dynamic balance training and functional ambulatory training.

06

What researchers measure

Primary outcomes

  1. Change in just noticeable difference threshold of proprioceptive sensitivity

    This experiment will use psychophysical methods to assess subject perception, the psychophysical methods developed two thresholds: detection threshold/absolute threshold and difference threshold/just noticeable difference threshold (JNDT). Difference threshold represents the minimum difference between two different intensity stimulation. In this experiment, the investigator will test the difference threshold for position sense and passive motion sense

    Time frame: baseline, 1 day and 4 weeks

  2. Change of position sense of the knee joint

    In the beginning, each subject sits comfortably in an arm chair (knee flexion 90o). The subject's non-affected leg is passively moved at three target angles (knee flexion 15, 30 and 70 degrees), and maintained the testing angle for 15 seconds before being return to knee flexion 90 degree (initial position). Subjects will be required to move the knee joint of the ipsilateral leg to the target angle. The assessor will use a hand-held goniometer to measure the angle of knee flexion. Each target angle will be measured three times, and both knee joints will be tested.

    Time frame: baseline, 1 day and 4 weeks

  3. Change of Unified Parkinson's disease rating scale-motor (UPDRS motor)

    Unified Parkinson's disease rating scale is used to evaluate the disease progression for Parkinson's disease (PD). Higher scores represent the more advanced disease progression. It includes four subscales: mentation, behavior and mood, activities of daily living, motor examination, and complications of therapy. In this study, the investigator mainly use the motor examination subscale. There are 14 items in motor examination including speech, facial expression, tremor at test, action or postural tremor of hands, rigidity, finger taps, postural stability, gait, body bradykinesia and hypokinesia...etc. The purpose is to evaluate the motor performance for individuals with PD (Movement Disorder Society Task Force on Rating Scales for Parkinson's, 2003).

    Time frame: baseline, 1 day and 4 weeks

  4. Change of balance function (measured by Functional Reach Test)

    The purpose of functional reach test is used to measure balance function. Participants can be in standing or sitting position (unable to stand). It measures the difference of distance in centimeters between arm's length with arms at 90° flexion and maximal forward reach with a fixed base of support.

    Time frame: baseline, 1 day and 4 weeks

  5. Change of mobility function (measured by Time up and go test)

    The purpose of time up and go test (TUG) is to evaluate the mobility function including both static and dynamic balance. The experimenter uses a stopwatch to measure the time that a person takes to rise from a chair, walk three meters, turn around, walk back to the chair, and sit down. Participants can walk independently or with walking devices. It is easy to administer and can applied to elderly population.

    Time frame: baseline, 1 day and 4 weeks

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Study locations

1 site
  • Chang Gung Memorial Hospital
    Linkou, 333, Taiwan
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 23, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03777501
Lead sponsor
Chang Gung University
Responsible party
Kuan-yi Li (Associate professor, Chang Gung University) — Principal investigator
First posted
Dec 17, 2018
Start date
Dec 28, 2018
Primary completion
Jun 28, 2019
Completion
Jun 28, 2019
Last update
Jan 23, 2020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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