Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
NCT05501210

Vibration on Patellofemoral Joint Pain After ACLR

Led by Chinese University of Hong Kong · Updated on 2026-03-18

50

Participants Needed

1

Research Sites

391 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Vibration on Patellofemoral Joint Pain After ACLR

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 to 60 years
  • Unilateral ACL reconstruction surgery
  • Persisting patellofemoral joint pain
  • Isolated symptomatic site or pathology
Not Eligible

You will not qualify if you...

  • Age over 60 years
  • Bilateral ACL reconstruction surgery
  • Revision ACL reconstruction surgery
  • Any rheumatological diseases
  • Previous injury to the opposite knee
  • Any knee osteoarthritis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Chinese University of Hong Kong

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

M

Michael Tim-Yun Ong, Prof.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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