Patellofemoral Pain Syndrome Clinical Trial
Official title:
A Prospective Randomized Study Comparing the Outcome of Electrical Stimulation of Vastus Medialis Obliquus Muscle and Physical Therapy vs Only Physical Therapy But no Electrical Stimulation in Patients With Patellofemoral Pain Syndrome
NCT number | NCT03184545 |
Other study ID # | 16-726 |
Secondary ID | |
Status | Recruiting |
Phase | Phase 3 |
First received | |
Last updated | |
Start date | July 24, 2017 |
Est. completion date | June 2026 |
The purpose of study is to evaluate the efficacy of the electrical muscle stimulation (EMS) device in patients with patellofemoral pain known as anterior knee pain. Usual treatment for it is physical therapy (PT). We want to evaluate and see if adding the electrical muscle stimulation will fasten the recovery and improved outcome in patellofemoral pain syndrome. Half of participants will receive EMS and PT while other half will receive PT only.
Status | Recruiting |
Enrollment | 92 |
Est. completion date | June 2026 |
Est. primary completion date | June 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility | Inclusion Criteria: - Bilateral/unilateral anterior knee pain for more than 3 moths - Age of patient 18 to 40 years - At least 3 of the 4 following criteria present: pain associated with prolonged sitting with knees bend, pain with going downstairs, kneeling and squatting or sports activities - No h/o injury - No h/o surgery to the knee Exclusion Criteria: - H/o patellar dislocation or subluxation - Associated bursitis, tendinitis in periarticular area - Ligamentous problems - Intra-articular pathology - Pregnancy (patient reported pregnancy, in case of doubt patient will be referred to their OBG/GYN physician to exclude the pregnancy) - H/o knee surgery - Oral or intraarticular administration of steroid medication with in last 3 months - Patients with implanted devices like pacemaker |
Country | Name | City | State |
---|---|---|---|
United States | New York Bone and Joint Specialists | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Northwell Health |
United States,
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* Note: There are 22 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Kujala patellofemoral score. | Assessment will be done at each visit (pre-treatment, post-start treatment 3 weeks,, 6 weeks, 12 weeks, 6 months and 12 months) based on Kujala patellofemoral score. The Kujala score assesses following points: Limp, support, walking, stairs, squatting,running, jumping, prolong sitting with knee flexed,pain,swelling,abnormal painful kneecap movements, atrophy of thigh and flexion deficiency. Repeated measures linear regression models will be used to compare the two treatment arms with respect to knee function, pain score, and muscle strength from baseline to 12 months.
Total duration of study is two years. We intend finish enrolling 92 patients by the end of one year after start of study. But each patient will be followed for total 12 months period. If any patient enrolled at 1 year mark after start of study , he will be followed for one year. |
2 years. Total duration of study is two years. But each patient will be followed for total 12 months after enrollment. If any patient enrolled at 1 year mark after start of study , he will be followed for one year. So total duration of study is 2 years. | |
Primary | Visual analog pain scale (VAS) pain scale during activities of life | VAS scale of 1-10 will be used to evaluate knee pain. 1 being mild and 10 being worst. | 2 years | |
Primary | Isometric strength measurement of knee | Isometric strength will be measured using dynamo-meter. | 2 years | |
Secondary | Secondary outcome measure would be how many return to sports activity. | Secondary outcome assessment will be to see how many in EMS+PT group and how many in PT group returned to their previous activity level of sports without any pain after completion of treatment. | 2 years | |
Secondary | At what point of time they returned to their sports activity | It will be also noted and compared between the groups at what time period after the start of treatment they returned to their regular sports activities. We hypothesize that EMS group might return early. | 2 years |
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