Emovi 3D Knee Assessment Device Intervention for Operational Readiness
Objective Dynamic and 3D Knee Assessment Medical Device to Improve Recovery and Accelerate Return to Readiness in Service Members With Knee Pain
Womack Army Medical Center
180 participants
Oct 24, 2024
INTERVENTIONAL
Conditions
Summary
This is a randomized clinical trial investigating the use of the Emovi Knee Kinesiography information in the treatment of anterior knee pain in physical therapy.
Eligibility
Inclusion Criteria3
- Age 18-50
- Active Duty Service Member stationed at Fort Liberty and Schofield Barracks
- Diagnosis of patellofemoral pain (ICD-10 codes: M25.2 (pain in unspecified knee), M25.561 (pain in right knee), and M25.562 (pain in left knee)
Exclusion Criteria6
- Pregnancy
- Known to be leaving that duty station within next 3 months
- Concurrent lower limb injuries (examples include but are not limited to ankle sprain or HS strain)
- Previous knee surgery
- History of traumatic knee injury, such as a ligament tear or meniscal tear
- Presence of rheumatoid or neurological disease
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Interventions
All participants will receive a KneeKG exam. This device will capture three-dimensional knee kinematics for a participant's knee, using the KneeKG system. Therapists will use these reports and suggested exercises to guide their care for participants in the Intervention group.
Locations(2)
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NCT06517056