Effect of Neuromuscular Training and Taping on Knee Pain from Flat Feet
Efficacy of Neuromuscular Training and Manual Therapy With Augmented Low-Dye Taping Technique for Correction of Pronated Foot in the Management of Anterior Knee Pain
This study is testing if a special training and taping method can help people with flat feet and knee pain feel better and move easier.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 35 Years |
| Sex | All |
| Sponsor | Mediclinic Al Noor Hospital Academic / other |
| Locations | 1 site (Abu Dhabi) |
| Trial ID | NCT05917080 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effectiveness of neuromuscular training and manual therapy combined with an augmented low-dye taping technique to correct pronated feet in patients suffering from anterior knee pain. The study aims to explore the biomechanical relationship between excessive foot pronation and anterior knee pain, as well as the potential benefits of therapeutic foot interventions. Participants will undergo specific interventions designed to address their foot alignment and knee pain symptoms, with assessments made on their pain levels and functional abilities.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18 to 35 with clinically diagnosed patellofemoral pain syndrome and excessive foot pronation.
Not a fit: Patients with a history of knee joint surgery, significant knee injuries, or certain medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce knee pain and improve mobility for patients with pronated feet.
How similar studies have performed: While the specific combination of interventions is novel, similar approaches targeting foot alignment and knee pain have shown promise in previous studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age - 18 to 35 years * Sex - both males \& females * Clinically diagnosed patient of PFPS with Pronated foot * Anterior or posterior pain in the knee area lasting for more than 12 weeks * Excessive calcaneal eversion measured at 6° in the relaxed posture * Score of between three and seven points on the numerical pain rating in activities of daily living Kujala Scale Point 40 \& Above Exclusion Criteria: * A history of diagnosis of meniscus or joint injury \& knee joint surgery * Taking nonsteroidal anti-inflammatory drugs or corticosteroids within 24 hrs before the test * History of brain injury or vestibular disorder within the last 6 months * Positive sign of Patellar Apprehension test * Congenital or traumatic deformity * Allergic reactions to taping * Concomitant diagnosis of pre patellar bursitis or tendonitis * knee Ligamentous injury or laxity * Plica syndrome \& Osgood Schlatter's disease * Malignancy \& Skin Infection * Pregnant woman or lactating women.
Where this trial is running
Abu Dhabi
- Mediclinic Al Noor Hospital — Abu Dhabi, United Arab Emirates (Recruiting)
Study contacts
- Study coordinator: Albert Anand.U, MPT
- Email: albertmpt@gmail.com
- Phone: 971 501224393
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.