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A Confirmatory Trial of Multidisciplinary Digital Therapeutics for Patellofemoral Pain Syndrome

Patellofemoral Pain Syndrome Clinical Trial

Official title:
Prospective, Randomized, Controlled Confirmatory Clinical Investigation to Evaluate the Safety and Efficacy of a Multidisciplinary Digital Therapeutics in Patients With Patellofemoral Pain Syndrome

Clinical Trial Summary

This randomized controlled confirmatory study will be evaluating an mobile application, MORA Cure (ETH-01K), owned by EverEx, Inc., to examine safety and effectiveness in individuals with patellofemoral pain syndrome.

Clinical Trial Description

This randomized controlled confirmatory study will enroll 216 participants, where half will be randomly assigned to the digital therapeutics (S/W medical device), MORA Cure (n = 108), and half will be assigned to treatment as usual (TAU) (n = 108), to examine safety and effectiveness in individuals with patellofemoral pain syndrome. All subjects will be followed up in the study for a total of 12 weeks, 8-week courses of treatment with additional 4-week observation. The application provides multidisciplinary rehabilitation treatment, a combination of graded exercise therapy and cognitive behavioural therapy for patients with patellofemoral pain syndrome. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06260865
Study type Interventional
Source EverEx Inc.
Contact Tae Hyun Park, MD
Phone 82-2-588-0812
Email bill@everex.co.kr
Status Not yet recruiting
Phase N/A
Start date March 31, 2024
Completion date August 30, 2024
View Details
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