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Wedged Insoles for Management of Knee Osteoarthritis

Primary Purpose

Knee Osteoarthritis

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
wedged insole
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Osteoarthritis, Cartilage, Musculoskeletal, Biomechanics, Subtype, Footwear, Orthotics, Joint Loading

Eligibility Criteria

40 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Physician-diagnosed knee osteoarthritis (using American College of Rheumatology clinical and radiographic criteria)
  • Kellgren-Lawrence grade 1, 2, 3 or 4
  • Primary symptoms and disease location must be attributed to medial tibiofemoral compartment
  • KOOS pain of 75 points or lower (where 0 is worst pain and 100 is no pain)

Exclusion Criteria:

  • X-ray older than 2 years
  • Viscosupplementation within past 6 months
  • Cortisone injection in past 3 months
  • Narcotic pain medication within past 3 months
  • Use of knee unloading brace interventions in past 2 months
  • Recent (past 6 months) knee or neuromuscular injury that could bias pain assessments or gait analysis results
  • No KAM reduction with either lateral or medial wedge insole

Sites / Locations

  • Human Performance Laboratory, University of Calgary

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Waitlist Control

Experimental wedged insole

Arm Description

A waitlist control condition, where the participant receives no insole for 3 months. During this 3 month period, the participant will continue to be monitored for outcome variables.

Either a medially wedged or laterally wedged footwear insole (whichever reduces knee joint mechanical loading more, as determined from subject-specific biomechanical tests), constructed using a 3D printer will be inserted into each participant's shoe. The participant will be asked to utilize this insole as much as possible throughout the day over the course of 3 months.

Outcomes

Primary Outcome Measures

KOOS pain score
Knee Injury and Osteoarthritis Outcome Score (KOOS) Pain subsection

Secondary Outcome Measures

Adiposity
Measured using Dual Energy X-Ray Absorptiometry (DXA) scan
Knee biomechanics
Other knee joint mechanical variables assessed using motion analysis (ex. varus thrust, knee adduction impulse).
PASE score
Physical Activity Scale for the Elderly (PASE)
UCLA Physical Activity Score
Scale evaluating physical activity levels
Knee Adduction Moment
Calculated using inverse dynamics
Footwear Comfort
Evaluated using 100mm visual analog scale
KOOS subsection and aggregate scores
All other KOOS sections (excluding pain, which is primary outcome)

Full Information

First Posted
February 18, 2014
Last Updated
November 30, 2015
Sponsor
University of Calgary
Collaborators
Canadian Institutes of Health Research (CIHR), Natural Sciences and Engineering Research Council, Canada, Alberta Innovates Health Solutions, Killam Trusts, New Balance Athletic Shoe, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02067208
Brief Title
Wedged Insoles for Management of Knee Osteoarthritis
Official Title
Reduced Knee Joint Loading With Lateral and Medial Wedge Insoles for Management of Knee Osteoarthritis: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
October 2014 (undefined)
Primary Completion Date
October 2015 (Actual)
Study Completion Date
November 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary
Collaborators
Canadian Institutes of Health Research (CIHR), Natural Sciences and Engineering Research Council, Canada, Alberta Innovates Health Solutions, Killam Trusts, New Balance Athletic Shoe, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Knee osteoarthritis (OA) is commonly treated using laterally wedged insoles. Although these insoles typically reduce knee abduction moments (KAM) - a variable associated with knee osteoarthritis - and thus are believed to be beneficial for OA management, recent research has indicated that in some cases lateral wedge insoles actually increase knee joint loads. In such cases, a medial wedge may be more appropriate. The purpose of this study is to evaluate the influence of reduced KAMs on pain over 3-months for patients with knee OA. It is hypothesized that pain reduction will be directly related to KAM reduction. Forty-six participants with knee OA will be recruited to participate. Each will undergo biomechanical gait analysis to determine the wedge type that most greatly reduces knee adduction moments. In addition, each participant will undergo a Dual Energy X-Ray Absorptiometry (DXA) scan to quantify adiposity. Finally, participants will complete a series of questionnaires to evaluate pain, function, physical activity, footwear comfort and injury history. Participants will be randomized into either a wait list control group (no insole) or experimental group (medial or lateral wedged insole), and monitored for 3 months. Changes to pain, function, comfort and physical activity from baseline to 3 months will be assessed within the control and experimental groups. Regression analyses will be conducted on the experimental group to determine if a relationship exists between reduced KAMs and reduced pain over 3 months. Comparisons will also be made between the control and experimental groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Osteoarthritis, Cartilage, Musculoskeletal, Biomechanics, Subtype, Footwear, Orthotics, Joint Loading

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Waitlist Control
Arm Type
No Intervention
Arm Description
A waitlist control condition, where the participant receives no insole for 3 months. During this 3 month period, the participant will continue to be monitored for outcome variables.
Arm Title
Experimental wedged insole
Arm Type
Experimental
Arm Description
Either a medially wedged or laterally wedged footwear insole (whichever reduces knee joint mechanical loading more, as determined from subject-specific biomechanical tests), constructed using a 3D printer will be inserted into each participant's shoe. The participant will be asked to utilize this insole as much as possible throughout the day over the course of 3 months.
Intervention Type
Device
Intervention Name(s)
wedged insole
Other Intervention Name(s)
orthotic
Intervention Description
Wedged insoles are designed to reduce frontal plane knee joint mechanical loads during gait. Specifically, they can alter the knee adduction moment during gait - a variable associated with progression of knee osteoarthritis. In the experimental arm of this study, participants will undergo biomechanical gait analysis to identify the wedged insole that reduces the moments the most. The two options are medial wedge, where the medial aspect of the foot is elevated relative to the lateral aspect, and the lateral wedge, where the lateral wedge is elevated relative to the medial aspect.
Primary Outcome Measure Information:
Title
KOOS pain score
Description
Knee Injury and Osteoarthritis Outcome Score (KOOS) Pain subsection
Time Frame
baseline, 1-month, 2-months, 3-months
Secondary Outcome Measure Information:
Title
Adiposity
Description
Measured using Dual Energy X-Ray Absorptiometry (DXA) scan
Time Frame
baseline
Title
Knee biomechanics
Description
Other knee joint mechanical variables assessed using motion analysis (ex. varus thrust, knee adduction impulse).
Time Frame
baseline
Title
PASE score
Description
Physical Activity Scale for the Elderly (PASE)
Time Frame
baseline, 1-month, 2-months, 3-months
Title
UCLA Physical Activity Score
Description
Scale evaluating physical activity levels
Time Frame
baseline, 1-month, 2-months, 3-months
Title
Knee Adduction Moment
Description
Calculated using inverse dynamics
Time Frame
baseline
Title
Footwear Comfort
Description
Evaluated using 100mm visual analog scale
Time Frame
baseline
Title
KOOS subsection and aggregate scores
Description
All other KOOS sections (excluding pain, which is primary outcome)
Time Frame
baseline, 1-month, 2-months, 3-months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Physician-diagnosed knee osteoarthritis (using American College of Rheumatology clinical and radiographic criteria) Kellgren-Lawrence grade 1, 2, 3 or 4 Primary symptoms and disease location must be attributed to medial tibiofemoral compartment KOOS pain of 75 points or lower (where 0 is worst pain and 100 is no pain) Exclusion Criteria: X-ray older than 2 years Viscosupplementation within past 6 months Cortisone injection in past 3 months Narcotic pain medication within past 3 months Use of knee unloading brace interventions in past 2 months Recent (past 6 months) knee or neuromuscular injury that could bias pain assessments or gait analysis results No KAM reduction with either lateral or medial wedge insole
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ryan T Lewinson, BSc
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kelsey HM Collins, BS
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Isabelle A Vallerand, BSc
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
J Preston Wiley, MD, MPE
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Linda J Woodhouse, PhD, PT
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Raylene A Reimer, PhD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jay T Worobets, PhD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Walter Herzog, PhD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Darren J Stefanyshyn, PhD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
Human Performance Laboratory, University of Calgary
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 1N4
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
27580080
Citation
Lewinson RT, Vallerand IA, Collins KH, Wiley JP, Lun VMY, Patel C, Woodhouse LJ, Reimer RA, Worobets JT, Herzog W, Stefanyshyn DJ. Reduced knee adduction moments for management of knee osteoarthritis:: A three month phase I/II randomized controlled trial. Gait Posture. 2016 Oct;50:60-68. doi: 10.1016/j.gaitpost.2016.08.027. Epub 2016 Aug 26.
Results Reference
derived
PubMed Identifier
25467955
Citation
Lewinson RT, Collins KH, Vallerand IA, Wiley JP, Woodhouse LJ, Reimer RA, Worobets JT, Herzog W, Stefanyshyn DJ. Reduced knee joint loading with lateral and medial wedge insoles for management of knee osteoarthritis: a protocol for a randomized controlled trial. BMC Musculoskelet Disord. 2014 Dec 3;15:405. doi: 10.1186/1471-2474-15-405.
Results Reference
derived

Learn more about this trial

Wedged Insoles for Management of Knee Osteoarthritis

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