Knee isometric exercise program for anterior knee pain
Effectiveness of a Knee Isometric Program on Reducing Anterior Knee Pain and Improving Functional Outcomes
NA · The Methodist Hospital Research Institute · NCT06536426
This study tests if a special knee exercise program can help people with anterior knee pain feel better compared to standard treatment.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | The Methodist Hospital Research Institute (other) |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT06536426 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a knee isometric program (KIP) compared to the standard treatment for anterior knee pain. Participants will be randomly assigned to either the KIP or a control group, ensuring that both groups receive similar experiences in terms of physical therapy sessions and exercise duration. The study will monitor participants' adherence to the exercise program and document any pain medication usage. The goal is to determine if the KIP can provide better outcomes for patients suffering from anterior knee pain.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-65 who have experienced anterior knee pain for at least 4 weeks but no longer than 12 months.
Not a fit: Patients with neurological or degenerative musculoskeletal conditions, recent surgeries, or those currently engaged in structured strength training may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could offer a more effective treatment option for patients with anterior knee pain.
How similar studies have performed: While similar approaches have been explored, the specific efficacy of the KIP compared to the current gold standard is being tested for the first time in this context.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Accept all provisions of the study and agree to complete the program in its entirety * Age between 18-65 * Complaint of anterior knee pain for at least 4 weeks, but no more than 12 months * Prescribed referral for physical therapy for their knee(s) from one of the investigators Exclusion Criteria: * Potential participant does not agree to comply with study protocols or does not wish to be subjected to a random group allocation * Any neurological or degenerative musculoskeletal condition involving the lower extremities * Ages outside of 18-65 * Surgical history or fracture within the last 12 months on the affected extremity(ies) * Currently participating in a structured strength training program * Inability to access clinic for data collection or follow-up sessions * Significant anatomical anomaly or limb alignment disorder as diagnosed by medical professional (femoral anteversion/retroversion, patella alta/baja, varus/valgus deformities, patella deformities/fractures, osteotomy procedures, limb lengthening procedures) * Significant cartilage damage as diagnosed by medical professional (grade 3+ chondral defects of the femur or patella) * Any other condition that limits full weight bearing of the affected lower extremity(ies) * Vulnerable populations
Where this trial is running
Houston, Texas
- Houston Methodist Research Institute — Houston, Texas, United States (RECRUITING)
Study contacts
- Study coordinator: Haley Goble, MHA
- Email: hmgoble@houstonmethodist.org
- Phone: 713-441-3930
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.
Conditions: Anterior Knee Pain Syndrome