Effects of a New Knee Brace for Treatment of the Knee Osteoarthritis

NCT01866176 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2014-03-06

No results posted yet for this study

Summary

The purpose of this study is to evaluate the immediate effects of a knee brace with a new mechanism on the pain and medial knee loading during gait among medial knee osteoarthritis patients. The effects of this new brace is compared to a stabilizing brace and a typical valgus knee brace. The investigators recruited 24 knee osteoarthritis and they have to wear each of the three braces during three months. A fifteen days wash-out period is given after each three months. Biomechanical evaluation is carried out before and after each three months. This evaluation consisted of three questionnaires (KOOS, WOMAC and Medical Outcome Score Short Form-36 (MOS-SF36)), a motion analysis with an optoelectronic system, then a 6-min walk test. During motion analysis, ten gait trials are executed without brace and ten with the brace.

Conditions

Interventions

DEVICE

Stabilizing Knee Brace

Brace with no valgus action

DEVICE

Valgus Knee Brace

Valgus brace with traditional three point bending system

DEVICE

New Knee Brace

Brace with new mechanism to decrease the knee loading.

Sponsors & Collaborators

  • Natural Sciences and Engineering Research Council, Canada

    collaborator OTHER
  • Fonds de la Recherche en Santé du Québec

    collaborator OTHER_GOV
  • Ergorecherche Inc.

    collaborator INDUSTRY
  • Laval University

    lead OTHER

Principal Investigators

  • Philippe Corbeil, PhD · Laval University

  • Yoann Dessery, MSc · Laval University

  • Étienne L Belzile, MD · Laval University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2013-05-31
Completion
2013-08-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

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 NCT01866176 on ClinicalTrials.gov