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Emovi 3D Knee Assessment Device Intervention for Operational Readiness

NCT06517056 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2025-07-16

No results posted yet for this study

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.

Conditions

  • Patellofemoral Pain
  • Patellofemoral Pain Syndrome

Interventions

DEVICE

Emovi Knee Kinesiography

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.

Sponsors & Collaborators

  • The Geneva Foundation

    collaborator OTHER

  • Womack Army Medical Center

    lead FED

Principal Investigators

  • Don L Goss, DPT, PhD · Womack Army Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-24
Primary Completion
2025-10-31
Completion
2025-10-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06517056 on ClinicalTrials.gov