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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

Who can join

Ages 18 to 50 · All sexes

Inclusion Criteria:

* 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 Criteria:

* 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

About the study

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.

What is being tested

• Emovi Knee Kinesiography (device)

Sponsor: Womack Army Medical Center · Participants: 180 · Started: Oct 24, 2024

Contact the study team

• Don L Goss, DPT, PhD · Phone: 9106033147

Official record on ClinicalTrials.gov — NCT06517056

Locations in the U.S.

Conditions

• Patellofemoral Pain Syndrome

From ClinicalTrials.gov, data retrieved Oct 1, 2026. Each study sets its own eligibility; the study team decides who can join.