Emovi 3D Knee Assessment Device Intervention for Operational Readiness

Part of paid clinical trials in Honolulu, Hawaii.

Sponsor
Womack Army Medical Center
Study ID
NCT06517056
Status
Recruiting
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Conditions

  • Patellofemoral Pain
  • Patellofemoral Pain Syndrome

Eligibility Criteria

Sex
ALL
Age
18 Years - 50 Years
Healthy Volunteers
Not accepted

Interventions

  • Emovi Knee Kinesiography — DEVICE
    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.

Study Details

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.

Key Dates

Start date
Oct 24, 2024
Status verified
Jul 2025
Primary completion
Oct 31, 2025
Completion
Oct 31, 2025

Study Design

Enrollment
180 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC

Arms

  • Experimental: Intervention: Knee KG informed physical therapy
    Participants in this group will receive care guided by the impairments identified with the KneeKG. The KneeKG exam results in recommended exercises that target the specific biomechanical impairments identified. The exercises and dose given to the participant will be based on what the KneeKG device recommends after the exam. The participant will be seen twice a week for 4 weeks.
  • No Intervention: Control: Standard of care physical therapy
    Participants in this arm will have their KneeKG data captured, but this information will not be provided to the physical therapist to inform their care. Instead, physical therapists will deliver care as they normally do in routine clinical practice. The participant will be seen twice a week for 4 weeks.

Primary Outcome Measure

Patient-Reported Outcomes Measurement Information System (PROMIS) Physical Function [ Time Frame: 12 weeks ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Tripler Army Medical CenterHonoluluHawaii96859
Dan Rhon
[email protected]
253-293-0154
Womack Army Medical CenterFort LibertyNorth Carolina28310
Don L Goss, DPT, PhD
[email protected]
910-603-3147

Find similar trials in Honolulu, HI

By research site
Tripler Army Medical Center· Honolulu, HIWomack Army Medical Center· Fort Liberty, NC

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