Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Recruiting NCT05614583

Multidisciplinary Digital Therapeutics of Patellofemoral Pain Syndrome Versus Usual Care

Conditions: Patellofemoral Pain Syndrome

Sex: All
Ages: 19 Years – 50 Years
Phase: NA
Enrollment: 40
Sponsor: EverEx Inc.

Location: Korea, Republic of

Summary

This randomized controlled pilot study will be evaluating an app, MORT-PFPS app (ETH-01K), owned by EverEx, Inc., to examine safety and effectiveness in individuals with patellofemoral pain syndrome.

Eligibility Criteria

Inclusion Criteria:Male or female ≥ 19 and <50 years of agePatients who have a history of anterior knee pain in one or both knees, persisting for longer than 3months but not longer than 2 yearsPatients who have pain provoked by squattingPatients who have pain provoked by 2 or more following activitieslong sittingcyclingrunninggoing up or down stairskneelingcompression of the patellapalpation of the patellar facetsPatients who signed a written informed consent formExclusion Criteria:Patients with osteoarthritis which scored 2 or higher grade of the Kellgren-Lawrence scalePatients who have a history of knee pathologies or injuries (fracture, tendon injury, cartilage injury, or patella dislocation)Patients who had previous knee surgeriesPatients who have patellar tendinopathyPatients who have Osgood-Schlatter disease, or other defined pathological conditions of the kneePatients who are pregnant or breastfeedingPatients who are using anti-inflammatory medicationPatients with known substance/alcohol use disordersPatients with known somatic symptom and related disordersPatients who are not able to participate in an exercise or strengthening program

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05614583). StuddyBuddy aggregates publicly available trial information.