Vibration on Patellofemoral Joint Pain After ACLR

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorChinese University of Hong Kong

About this trial

Anterior cruciate ligament (ACL) injury is a prevailing problem among sports participants, especially in non-contact sports. Studies have reported that 70-84% of ACL injuries are non-contact in nature, and movements like changing in direction while running, cutting and pivoting on a planted foot have resulted in a majority of ACL injuries. Even after ACL reconstruction (ACLR) surgeries, study has reported a 30-50% prevalence of developing patellofemoral joint (PFJ) pain in 1-2 years post-operation. Whole body vibration (WBV) therapy has been gaining attention as an effective method of training in recent years. It has been proved to have a positive effect on improving muscle strength, muscle activities, muscle power and loading during drop jump. Though duration of WBV may differ according to the effect of interest, several studies have had positive results with a 8 week WBV therapy in increasing muscle strength, proprioception, and post-ACLR knee functions. Further investigation on the underlying mechanism and possible application are to be continued to explore more possibilities with the WBV therapy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age between 18 to 60

Unilateral ACLR

Persisting PFJ pain

Isolated symptomatic site or pathology

Disqualifiers

Age > 60

Bilateral ACLR

Revision ACLR

Any rheumatological diseases

Trial design

Design model

Parallel

Treatments tested in this trial

  • WBV

    Device

    Whole body vibration (WBV) therapy

  • PEMF

    Device

    Pulsed electromagnetic fields (PEMF)

Treatment groups

50 Participants
are divided into 3 treatment groups
Group A: WBV + PEMF GroupExperimental treatment 2 interventions
Group B: Control GroupNo intervention 0 interventions
Group C: WBV onlyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change of The Knee injury and Osteoarthritis Outcome Score Patellofemoral subscale (KOOS-PF)

The KOOS-PF was developed to evaluate individuals or samples of individuals who present with anterior knee pain/patellofemoral pain and/or patellofemoral OA. It contains 11 items with 3 subscale : Stiffness, Pain, Quality of life (QOL).

Time frame
pre intervention and 8 weeks post intervention

Secondary outcomes

1

Isokinetic muscle strength

The subjects will be asked to test the muscle strength by using the isokinetic device (Biodex System 4; Biodex Medical Systems, Inc, Shirley, NY). Before testing, the subjects will be asked to have a 10-minute warm-up on a stationary bike at low intensity. By recommendation they will be asked to exert maximal concentric contraction of knee flexor and rt with the dynamometer at angular velocity of 60°/s for five times.

Time frame
pre intervention and 8 weeks post intervention
2

Muscle thickness

Muscle thickness of rectus femoris, vastus medialis, vastus lateralis and vastus intermedius will be assessed using ultrasound imaging. The ultrasound transducer will be placed at the muscle bellies to obtain an image of the cross-session of the muscle. The depth of the related muscle cross-session will be measured to represent the thickness of the muscle. Muscle thickness of rectus femoris, vastus medialis, vastus lateralis and vastus intermedius will be assessed using ultrasound imaging. The ultrasound transducer will be placed at the muscle bellies to obtain an image of the cross-session of the muscle. The depth of the related muscle cross-session will be measured to represent the thickness of the muscle.

Time frame
pre intervention and 8 weeks post intervention
3

The Numeric Pain Rating Scale (NPRS)

The Numeric Pain Rating Scale (NPRS): The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain. The 11-point numeric scale ranges from '0' representing "no pain" to '10' representing "the most severe pain imaginable". Scores range from 0-10 points, with higher scores indicating greater pain intensity.

Time frame
pre intervention and 8 weeks post intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.