Effect of Whole Body Vibration on Knee Pain and Function
Impact Of Whole Body Vibration on Planter /Dorsi Flexor Ratio, Pain and Functional Activities in Patellofemoral Pain Syndrome: Randomized Controlled Trial
This study is testing whether whole body vibration can help young adults with knee pain feel better and improve their movement compared to regular exercise.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | All |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Giza) |
| Trial ID | NCT06017778 on ClinicalTrials.gov |
What this trial studies
This study investigates the impact of whole body vibration (WBV) on individuals suffering from patellofemoral pain syndrome (PFPS). Participants aged 18-35 with knee pain will be enrolled and divided into groups receiving either WBV or traditional exercise treatments. The study aims to assess changes in the planter/dorsi flexor ratio, pain levels, and functional activities over time. The effectiveness of WBV as an intervention for PFPS will be evaluated, as current evidence is limited.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-35 experiencing anterior knee pain during activities like running or squatting for at least six weeks.
Not a fit: Patients with other knee conditions, a history of knee surgery, or systemic conditions affecting the musculoskeletal system may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could provide a new, effective treatment option for reducing pain and improving function in patients with PFPS.
How similar studies have performed: While some studies have shown positive effects of WBV on muscle strength and balance, the specific application for PFPS remains largely untested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age: Adults aged 18 -35 years 2. Symptoms: Pain in the anterior or retro patellar knee region during activities such as running, jumping, squatting, or prolonged sitting 3. Duration: Pain lasting at least 6 weeks Exclusion Criteria: 1. Presence of other knee conditions: Individuals with PFPS who also have other knee conditions such as ligament or meniscal injuries, osteoarthritis, or patellar tendinopathy may be excluded. 2. History of knee surgery: Patients who have undergone any knee surgery may be excluded as this may affect the outcomes of the study. 3. Systemic conditions: Patients with systemic conditions that may affect the musculoskeletal system such as rheumatoid arthritis or lupus may be excluded. 4. Pregnancy: Pregnant women with PFPS may be excluded as pregnancy may affect the outcomes of the study. 5. Inability to comply with study requirements: Patients who are unable to comply with the study requirements such as attending follow-up appointments or completing questionnaires may be excluded.
Where this trial is running
Giza
- Faculty of physical therapy , cairo university — Giza, Egypt (Recruiting)
Study contacts
- Study coordinator: Radwa Elshorbagy
- Email: Rtelshorbagy@ju.edu.sa
- Phone: 00966500920691
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.