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Gait Retraining to Reduce Joint Loading, Inflammation, and PTOA Risk

NCT03551678 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2020-10-27

No results posted yet for this study

Summary

The purpose of this study is to determine changes to knee joint loading, biological markers, and cartilage structure following a novel active feedback gait retraining program in anterior cruciate ligament reconstructed patients.

Conditions

  • Anterior Cruciate Ligament Reconstruction

Interventions

DEVICE

Active feedback gait retraining

The device measures pressure/force under the lateral side of the foot and activates vibration if loading crosses a set threshold. The location of the vibration is customized for each subject to achieve maximal sensitivity.

Sponsors & Collaborators

  • United States Department of Defense

    collaborator FED

  • VA Palo Alto Health Care System

    lead FED

Principal Investigators

  • Constance Chu, MD · VAPAHCS and Stanford University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2019-06-21
Primary Completion
2022-12-31
Completion
2022-12-31
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 NCT03551678 on ClinicalTrials.gov