Skip to main content
OpenTrials
Completed

NCT Number: NCT01300182

The Effect of Early WBVT on Neuromuscular Control After ACLR

To investigate the effect of early WBVT on neuromuscular control after ACLR.

Completed

Looking for future studies?

Notify Me

Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Physiotherapy Department, Prince of Wales Hospital

Shatin, Hong Kong, 852

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Whole body vibration therapy

Other

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.

Other names: Fitvibe Excel Pro - model number: 332015 (N.V. GymnaYniphy, Bilzen, Belgium)

Control

Other

Conventional post-operative physical therapy exercises and rehabilitation.

Primary outcomes

  1. Joint position sense

    Time frame: 1-month post-operation, 3-months post-operation, 6-months post-operation

    Using Biodex Dynamometer (Biodex Medical Systems, Shirley, NY, USA) for measurement.

  2. Muscle isokinetic strength

    Time frame: Pre-operation, 3-months post-operation, 6-months post-operation

    Using Cybex NORM dynamometer for measurement.

  3. Postural control

    Time frame: 1-month post-operation, 3-months post-operation, 6-months post-operation

    Using Biodex Stability System (BSS; Biodex Medical Systems, Shirley, NY, USA with software version 3.1) for measurement

  4. Functional Outcome

    Time frame: Pre-operation and 6-months post-operation

    Functional Outcomes

    • single leg hop test
    • triple leg hop test
    • caricoca test
    • Shuttle run test
  5. Knee joint stability

    Time frame: Pre-operation, 3-months post-operation, 6-months post-operation

  6. Knee range of motion

    Time frame: 6-months post operation

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Registry information

Official study title

The Effect of Early Whole-Body Vibration Therapy on Neuromuscular Control After Anterior Cruciate Ligament Reconstruction

Acronym: WBVT

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Feb 21, 2011
Registry last updated
Feb 13, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.