The Effect of Early WBVT on Neuromuscular Control After ACLR (WBVT)
Primary Purpose
Rupture of Anterior Cruciate Ligament
Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Whole body vibration therapy
Control
Sponsored by
About this trial
This is an interventional treatment trial for Rupture of Anterior Cruciate Ligament focused on measuring ACLR
Eligibility Criteria
Inclusion Criteria:
- ACLR with a single-bundle approach
- no complication such as wound infection after the ACLR
- able to walk with a pair of elbow crutches independently at one month post operation
Exclusion Criteria:
- concomitant posterior cruciate ligament, lateral collateral ligament, and medial collateral ligament injury in the same knee
- previous operation on either lower limbs
- medical problems such as pregnancy, acute thrombosis, serious cardiovascular disease, pacemaker, acute hernia, discopathy, spondylolysis, severe diabetes, epilepsy, recent infections, severe migraine, tumors or kidney stones etc
- neurological conditions such as Guillain-Barre ́ syndrome, myasthenia gravis, and postpolio syndrome
- prior experience of WBVT
Sites / Locations
- Physiotherapy Department, Prince of Wales Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Whole body vibration therapy
Control
Arm Description
Whole body vibration therapy on top of conventional physiotherapy treatment.
Conventional post-operative physical therapy rehabilitation exercises.
Outcomes
Primary Outcome Measures
Joint position sense
Using Biodex Dynamometer (Biodex Medical Systems, Shirley, NY, USA) for measurement.
Muscle isokinetic strength
Using Cybex NORM dynamometer for measurement.
Postural control
Using Biodex Stability System (BSS; Biodex Medical Systems, Shirley, NY, USA with software version 3.1) for measurement
Functional Outcome
Functional Outcomes
single leg hop test
triple leg hop test
caricoca test
Shuttle run test
Knee joint stability
Knee range of motion
Secondary Outcome Measures
Full Information
NCT ID
NCT01300182
First Posted
February 18, 2011
Last Updated
February 12, 2013
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT01300182
Brief Title
The Effect of Early WBVT on Neuromuscular Control After ACLR
Acronym
WBVT
Official Title
The Effect of Early Whole-Body Vibration Therapy on Neuromuscular Control After Anterior Cruciate Ligament Reconstruction
Study Type
Interventional
2. Study Status
Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
November 2010 (undefined)
Primary Completion Date
February 2012 (Actual)
Study Completion Date
February 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To investigate the effect of early WBVT on neuromuscular control after ACLR.
Detailed Description
The knee joint position sense, postural control, muscular strength and functional ability after anterior cruciate ligament construction (ACLR) are distorted, and even after a period of rehabilitation.
Previous studies had demonstrated that there was improvement in knee joint, postural balance, muscle strength and functional outcome in elderly, stroke and spastic patients already. It has also been concluded that the balance in elderly, postmenopausal women, Parkinson's disease, multiple sclerosis, stroke and spastic patients were all significantly improved. Some studies showed that the proprioception in osteoarthritis patients significantly improve. Knee strength is also one of the aspect being improved.
However, no studies focus on the early effect of WBVT on knee joint proprioception, postural control, muscle strength, knee joint stability and functional ability in ACLR cases. This study is to answer this research gap.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rupture of Anterior Cruciate Ligament
Keywords
ACLR
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
48 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Whole body vibration therapy
Arm Type
Experimental
Arm Description
Whole body vibration therapy on top of conventional physiotherapy treatment.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Conventional post-operative physical therapy rehabilitation exercises.
Intervention Type
Other
Intervention Name(s)
Whole body vibration therapy
Other Intervention Name(s)
Fitvibe Excel Pro - model number: 332015 (N.V. GymnaYniphy, Bilzen, Belgium)
Intervention Description
The WBVT will be carried out in a vibration plates operated in vertical direction. The frequency of that vibration can be adjusted step of 5Hz with vibration frequency ranges from 20Hz to 60Hz. The amplitude can be set as 4mm.
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Conventional post-operative physical therapy exercises and rehabilitation.
Primary Outcome Measure Information:
Title
Joint position sense
Description
Using Biodex Dynamometer (Biodex Medical Systems, Shirley, NY, USA) for measurement.
Time Frame
1-month post-operation, 3-months post-operation, 6-months post-operation
Title
Muscle isokinetic strength
Description
Using Cybex NORM dynamometer for measurement.
Time Frame
Pre-operation, 3-months post-operation, 6-months post-operation
Title
Postural control
Description
Using Biodex Stability System (BSS; Biodex Medical Systems, Shirley, NY, USA with software version 3.1) for measurement
Time Frame
1-month post-operation, 3-months post-operation, 6-months post-operation
Title
Functional Outcome
Description
Functional Outcomes
single leg hop test
triple leg hop test
caricoca test
Shuttle run test
Time Frame
Pre-operation and 6-months post-operation
Title
Knee joint stability
Time Frame
Pre-operation, 3-months post-operation, 6-months post-operation
Title
Knee range of motion
Time Frame
6-months post operation
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ACLR with a single-bundle approach
no complication such as wound infection after the ACLR
able to walk with a pair of elbow crutches independently at one month post operation
Exclusion Criteria:
concomitant posterior cruciate ligament, lateral collateral ligament, and medial collateral ligament injury in the same knee
previous operation on either lower limbs
medical problems such as pregnancy, acute thrombosis, serious cardiovascular disease, pacemaker, acute hernia, discopathy, spondylolysis, severe diabetes, epilepsy, recent infections, severe migraine, tumors or kidney stones etc
neurological conditions such as Guillain-Barre ́ syndrome, myasthenia gravis, and postpolio syndrome
prior experience of WBVT
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chak Lun Allan Fu
Organizational Affiliation
Physiotherapy Department, Prince of Wales Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Physiotherapy Department, Prince of Wales Hospital
City
Shatin
ZIP/Postal Code
852
Country
Hong Kong
12. IPD Sharing Statement
Learn more about this trial
The Effect of Early WBVT on Neuromuscular Control After ACLR
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