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NCT06517056 · ClinicalTrials.gov registry record · NA
Emovi 3D Knee Assessment Device Intervention for Operational Readiness
A NA study of Patellofemoral Pain Syndrome and Patellofemoral Pain, sponsored by Womack Army Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 180
- Enrollment target
- 2
- Study locations
NCT06517056: Recruiting NA study of Patellofemoral Pain Syndrome and Patellofemoral Pain, sponsored by Womack Army Medical Center.
NCT06517056 is a NA study of Patellofemoral Pain Syndrome and Patellofemoral Pain that is actively recruiting participants, run by Womack Army Medical Center. The registered enrollment target is 180 participants, above the 128-participant average among 10 other Patellofemoral Pain Syndrome trials with a reported enrollment target (41% higher). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06517056, a NA study of Patellofemoral Pain Syndrome and Patellofemoral Pain, is actively recruiting participants, sponsored by Womack Army Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 180 participants
- Enrollment target
- 2
- Study locations
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.
Primary Outcome
PROMIS asks patients about their functional ability, and symptoms. This tool is designed as a health-focused rather than a disease-focused measurement system. The primary outcome measure will focus on the the Physical Function domains since PFPS is known to limit function during daily and sports \& recreation activities. This is an adaptive questionnaire that is taken in RedCap and contains up to 166 questions that will not all be asked, scored 1-5 on a Likert scale based on limits of function.
Conditions Studied
Interventions
- DEVICE Emovi Knee Kinesiography
Study Locations (2)
Hawaii
- Tripler Army Medical Center - Honolulu
North Carolina
- Womack Army Medical Center - Fort Liberty
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 180 participants |
| Start Date | 2024-10-24 |
| Est. Completion | 2025-10 |
| Phase | NA |
What NCT06517056 shows while recruiting
NCT06517056 is an interventional study that assigns participants to a tested intervention. The registered 180 participants enrollment target is mid-sized for trials with a published cap, above the 128-participant average among 10 other Patellofemoral Pain Syndrome trials with a reported enrollment target (41% higher).
The record links to 2 conditions, with Patellofemoral Pain Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Emovi Knee Kinesiography is the first listed.
NCT06517056 reports a single indexed study location in Hawaii, North Carolina.
Frequently Asked Questions
What is clinical trial NCT06517056 about?
NCT06517056 is a clinical study titled "Emovi 3D Knee Assessment Device Intervention for Operational Readiness". 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 the current status of trial NCT06517056?
This trial is currently recruiting. It is a NA study. The enrollment target is 180 participants. The study started on 2024-10-24. Estimated completion is 2025-10.
What conditions does trial NCT06517056 study?
This clinical trial studies the following conditions: Patellofemoral Pain Syndrome, Patellofemoral Pain.
What interventions are being tested in trial NCT06517056?
The interventions under investigation include: Emovi Knee Kinesiography (DEVICE).
Who is sponsoring clinical trial NCT06517056?
This trial is sponsored by Womack Army Medical Center, which has 7 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06517056 being conducted?
This trial has 2 study locations across Hawaii, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Patellofemoral Pain Syndrome
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06517056's enrollment target sits among peer trials
180 2nd of 10 the highest of 10 other Patellofemoral Pain Syndrome trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Patellofemoral Pain Syndrome trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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