Vibration therapy for knee pain after ACL surgery
The Effect of Whole-Body Vibration on Patellofemoral Joint Pain After Anterior Cruciate Ligament Reconstruction
This study is testing if whole body vibration therapy can help people aged 18 to 60 recover better from knee pain after ACL surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Chinese University of Hong Kong Academic / other |
| Locations | 1 site (Hong Kong) |
| Trial ID | NCT05501210 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of whole body vibration (WBV) therapy on patients who have undergone anterior cruciate ligament reconstruction (ACLR) and are experiencing patellofemoral joint (PFJ) pain. It aims to assess whether WBV can improve muscle strength, proprioception, and overall knee function in these patients. The study will include individuals aged 18 to 60 with unilateral ACLR and persistent PFJ pain, while excluding those with certain knee conditions or previous injuries. The intervention will last for eight weeks, focusing on enhancing recovery and reducing pain.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 18 to 60 who have undergone unilateral ACLR and are experiencing ongoing PFJ pain.
Not a fit: Patients over 60 years old, those with bilateral ACLR, or individuals with knee osteoarthritis may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve recovery outcomes and quality of life for patients suffering from knee pain after ACL surgery.
How similar studies have performed: Previous studies have shown positive results with WBV therapy in improving muscle strength and knee function, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age between 18 to 60 2. Unilateral ACLR 3. Persisting PFJ pain 4. Isolated symptomatic site or pathology Exclusion Criteria: 1. Age \> 60 2. Bilateral ACLR 3. Revision ACLR 4. Any rheumatological diseases 5. Previous contralateral knee injury 6. Any knee osteoarthritis
Where this trial is running
Hong Kong
- The Chinese University of Hong Kong — Hong Kong, Hong Kong (Recruiting)
Study contacts
- Study coordinator: Michael Tim-Yun Ong, Prof.
- Email: michael.ong@cuhk.edu.hk
- Phone: 85235052723
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.