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Effects of Whole Body Vibration in Subacute Stroke Patients
This study is currently recruiting participants.
Verified by The Hong Kong Polytechnic University, November 2008
Sponsors and Collaborators: The Hong Kong Polytechnic University
Tung Wah Hospital
Information provided by: The Hong Kong Polytechnic University
ClinicalTrials.gov Identifier: NCT00796237
  Purpose

The overall aim of the proposed study is to determine whether whole body vibration is beneficial in promoting bone turnover, physical fitness and neuromotor performance in patients with subacute stroke.


Condition Intervention
Stroke
Device: Whole body vibration therapy
Other: standing on the vibration platform but no vibration will be applied

MedlinePlus related topics: Exercise and Physical Fitness
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind (Outcomes Assessor), Parallel Assignment
Official Title: Effects of Whole Body Vibration Training on Bone Health, Physical Fitness, and Neuromotor Performance in Individuals With Subacute Stroke: a Randomized Controlled Trial

Further study details as provided by The Hong Kong Polytechnic University:

Primary Outcome Measures:
  • Level of bone resorption marker CTx [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]
  • Level of bone formation marker, BSAP [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Six minute walk test [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]
  • Ankle arm index [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]
  • Functional Ambulation category [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]
  • Leg muscle strength (hand-held dynamometry) [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]
  • Berg Balance Scale [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]
  • Modified Ashworth Scale of Spasticity [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]
  • Sensory threshold to light touch in the foot [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]
  • Fugl-Meyer Motor Assessment [ Time Frame: baseline, immediately after treatment, and 2-month follow-up ] [ Designated as safety issue: No ]

Estimated Enrollment: 60
Study Start Date: May 2008
Estimated Study Completion Date: December 2011
Estimated Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
WBV: Experimental
In their regular physiotherapy sessions, the subjects in the experimental group will receive whole body vibration therapy for a duration of 4 weeks during their stay in the Tung Wah Hospital.
Device: Whole body vibration therapy
In their regular physiotherapy sessions, the subjects in the experimental group will receive WBV (20-240Hz, 10-minute sessions, 1 session per day, 5 sessions per week). The vibration loading will be carried out using the Fit-Vibe System (Germany), which is a vibration platform that is capable of generating vertical vibration.
CON: Active Comparator
The subjects in this group will not receive whole body vibration therapy.
Other: standing on the vibration platform but no vibration will be applied
The subjects in this group will perform the same exercises on the vibration platform as in the experimental group for the same duration, but no vibration will be given.

Detailed Description:

Brief periods of Whole body vibration(WBV) have been shown to improve bone density in post-menopausal women and children with cerebral palsy. In addition to the apparent benefits on bone health, WBV has been shown to increase muscle strength, postural control, muscular blood flow and oxygen uptake in various populations. Therefore, WBV can potentially be used as a tool to improve muscle strength, balance, and cardiovascular performance, especially for those with relatively low level of functioning. Stroke patients are therefore possible beneficiaries of WBV, as they often demonstrate muscle weakness, balance deficits, and poor cardiovascular function, in addition to bone loss. Only one pilot study has examined the effects of WBV in stroke patients. Van Nes et al.showed that postural stability in chronic stroke patients is improved after a few minutes of WBV at 30Hz and 3mm amplitude. The overall aim of the proposed study is to determine whether whole body vibration is beneficial in promoting bone turnover, physical fitness and neuromotor performance in patients with subacute stroke.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • diagnosis of stroke
  • medically stable
  • able to understand simple verbal commands
  • of chinese origin

Exclusion Criteria:

  • previous stroke in addition to the current admission
  • other neurological conditions, in addition to stroke
  • significant musculoskeletal or vascular conditions in the lower extremity
  • metal implants in the lower extremity
  • previous fracture in the lower extremity
  • are taking or were taking bone resorption inhibitors
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00796237

Contacts
Contact: Ricky WK Lau, MSc 85298743644 rsricky@inet.polyu.edu.hk

Locations
Hong Kong
Tung Wah Hospital Recruiting
Hong Kong, Hong Kong
Contact: Leonard SW Li, MD         lswli@hkucc.hku.hk    
Principal Investigator: Leonard SW Li, MD            
Sub-Investigator: Felix HF Chung, MSc            
Sub-Investigator: Ricky WK Lau, MSc            
Sponsors and Collaborators
The Hong Kong Polytechnic University
Tung Wah Hospital
Investigators
Principal Investigator: Marco YC Pang, PhD Hong Kong Polytechnic University
  More Information

Publications:
Responsible Party: Hong Kong Polytechnic University ( Marco Yiu-Chung Pang )
Study ID Numbers: UW-08-032
Study First Received: November 21, 2008
Last Updated: November 21, 2008
ClinicalTrials.gov Identifier: NCT00796237  
Health Authority: Hong Kong: Ethics Committee

Keywords provided by The Hong Kong Polytechnic University:
stroke
bone
gait
muscle
vibration
motor balance

Study placed in the following topic categories:
Cerebral Infarction
Stroke
Vascular Diseases
Brain Ischemia
Central Nervous System Diseases
Ischemia
Brain Infarction
Brain Diseases
Infarction
Cerebrovascular Disorders

Additional relevant MeSH terms:
Nervous System Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 15, 2009