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OpenTrials
Completed

NCT Number: NCT01866176

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

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.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Pavillon de l'Éducation Physique et des Sports - Université Laval

Québec, Quebec, G1V 0A6, Canada

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Symptomatic medial knee OA (Kellgren-Lawrence grade I, II or III) according to clinical and radiological criteria of the American College of Rheumatology
  • Knee pain > 31/100 (Western Ontario and McMaster Universities Arthritis Index - WOMAC)
  • Moderately active
  • Varus knee alignment equal or superior to 2°

Exclusion criteria

  • Severe knee OA (K-L grade IV)
  • Rheumatoid arthritis or other inflammatory arthritis
  • Avascular necrosis
  • History of periarticular fracture or septic arthritis
  • Bone metabolic disease
  • Pigmented villonodular synovitis
  • Cartilaginous disease
  • Neuropathic arthropathy
  • Synovial osteochondromatosis
  • Total or partial knee arthroplasty
  • Flexion contracture of ipsi- or contra-lateral knee greater than 15°
  • Hip or ankle joint damage with mobility limitation
  • Obesity (BMI ≥ 40)
  • Intra-articular corticosteroids injection in the affected knee during the two previous months
  • Reduced mobility (Charnley class C)

Treatment and study plan

Stabilizing Knee Brace

Device

Brace with no valgus action

Valgus Knee Brace

Device

Valgus brace with traditional three point bending system

New Knee Brace

Device

Brace with new mechanism to decrease the knee loading.

Primary outcomes

  1. Change in Knee adduction moment

    Time frame: Change from Baseline at 3 months

  2. Change in Knee pain

    Time frame: Change from Baseline at 3 months

    A 20-cm visual analog scale (0-100) is used to assess pain.

Secondary outcomes

  1. Change in Spatiotemporal gait parameters

    Time frame: Change from Baseline at 3 months

    Test of the gait symmetry with the gait phase duration and step length.

  2. Change in Gait velocity

    Time frame: Change from Baseline at 3 months

  3. Change in Knee adduction angle

    Time frame: Change from Baseline at 3 months

  4. Change in Knee brace comfort

    Time frame: Change from Baseline at 3 months

    A 20-cm visual analog scale (0-100) is used to assess comfort.

Sponsors and collaborators

Lead sponsor

Laval University

Other

Collaborators

  • Ergorecherche Inc.
  • Fonds de la Recherche en Santé du Québec
  • Natural Sciences and Engineering Research Council, Canada

Registry information

Official study title

Effects of a New Knee Brace for Treatment of the Knee Osteoarthritis on the Medial Knee Loading During Gait

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
May 31, 2013
Registry last updated
Mar 6, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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