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Knee Brace and Biomechanical Footwear in the Treatment of Knee Osteoarthritis.

Primary Purpose

Osteoarthritis,Knee

Status
Completed
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Home-based exercise
Knee brace
Biomechanical footwear device
Sponsored by
Central Finland Hospital District
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis,Knee focused on measuring Knee brace, biomechanical footwear, exercise, RCT

Eligibility Criteria

45 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • moderate or severe knee pain (>40mm on a VAS scale 0-100mm)
  • radiographic knee osteoarthritis (Kellgren-Lawrence grades 1-3)
  • age between 45 and 70 years

Exclusion Criteria:

  • inflammatory joint disease
  • acute (<6 months) knee trauma
  • arthroscopic surgery in the past six months
  • a planned knee replacement surgery or other planned surgical treatment of the knee
  • knee injections in the past 3 months
  • superficial wounds at the knee area
  • arterial insufficiency
  • severe varicosities
  • impaired vision
  • postural difficulties
  • body-mass index (BMI) >35kg/m2
  • fibromyalgia
  • rheumatoid arthritis or other active rheumatoid inflammatory disease.

Sites / Locations

  • Central Finland Central Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Exercise therapy group

Knee brace and exercise group

Footwear device group

Arm Description

(n = 40)

(n = 40)

(n = 40)

Outcomes

Primary Outcome Measures

Change from baseline Pain intensity at 4 months: VAS
Visual Analog Scale for Pain (score of 100 mm). No pain (score of 0), worst imaginable pain (score of 100).

Secondary Outcome Measures

Change from baseline clinical symptoms at 4 months.
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)-questionnaire evaluates the condition of patients with knee osteoarthritis including pain, stiffness and physical function. In the subscale of pain (score range 0 - 500), stiffness (score range 0 - 200), and functional limitation (score range 0 - 1700) lower values represent a better outcome. In order to normalize each score on 0 - 100 scales, the following correction factors are used: pain 0.20, stiffness 0.50, functional limitation 0.059.
Change from baseline Health-Related Quality of Life at 4 months: SF-36
The SF-36-Item Health Survey measures Health-Related Quality of Life. The SF-36 is a multi-item scale assessing eight health concepts: 1) limitations in physical activities, 2) limitations in social activities, 3) limitations in usual role activities, 4) bodily pain, 5) general mental health, 6) limitations in usual role activities, 7) vitality, and 8) general health perceptions, with scores for each dimensions ranging from 0 (poor health) to 100 (good health).
Change from baseline isometric knee extension and flexion forces at 4 months.
Will be measured with dynamometer
Change from baseline walking speed gait parameter at 4 months.
Walking speed (cm/sec) will be measured by the instrumented walkway system (GAITRite mat).
Change from baseline cadence gait parameter at 4 months.
Cadence (steps per minute) will be measured by the instrumented walkway system (GAITRite mat).
Change from baseline stride length gait parameter at 4 months.
Stride length, i.e., the distance between 2 successive placement of the same foot (cm) will be measured by the instrumented walkway system (GAITRite mat).
Change from baseline step length gait parameter at 4 months.
Step length, i.e., the distance measured from the heel point of one foot to the heel point of the other foot (cm) will be measured by the instrumented walkway system (GAITRite mat).
Change from baseline stance time and % stance gait parameter at 4 months.
Stance time (sec) and % stance will be measured by the instrumented walkway system (GAITRite mat).
Change from baseline swing time and % swing gait parameter at 4 months.
Swing time (sec) and % swing will be measured by the instrumented walkway system (GAITRite mat).
Change from baseline 40 m Fast-paced Walk Test at 4 months.
A fast-paced walking test that is timed over 4 x 10m for a total 40 m
Change from baseline Stair Ascend/Descend Test at 4 months.
The time (sec) it takes to ascend and descend a flight of stairs. The total time to ascend and descend steps (negative number indicates better performance) will be recorded and reported
Change from baseline 30s Timed Chair Stand Test at 4 months.
The maximum number of chair stand repetitions possible in a 30 second period. The total number of chair stands (up and down equals one stand) completed in 30 seconds will be reported.
Change from baseline knee range of movement at 4 months.
Will be measured with goniometer
Change from baseline physical activity at 4 months.
The short form of International Physical Activity (IPAQ-SF) questionnaire measures data on Health-Related Physical Activity. The IPAQ-SF Records the activity of four intensity levels (vigorous-intensity, moderate-intensity, walking, sitting) for the last 7 days. Results are reported as a continuous variable (MET minutes a week). To calculate MET minutes a week the MET value given (walking = 3.3, moderate activity = 4, vigorous activity = 8) is multiplied by the minutes the activity was carried out and again by the number of days that the activity was undertaken. To get total MET minutes of physical activity a week, the MET minutes achieved in each category are added together. Higher MET-values represent better outcome.
Change from baseline cost-utility at 4 months.
Will be measured with the items of the SF-6D questionnaire, which in turn can be converted from the items of the SF-36 questionnaire. The SF-6D score varies from 0 to 1, 0 representing worst health cost-utility and 1 best health utility.

Full Information

First Posted
January 30, 2017
Last Updated
January 30, 2020
Sponsor
Central Finland Hospital District
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1. Study Identification

Unique Protocol Identification Number
NCT03684850
Brief Title
Knee Brace and Biomechanical Footwear in the Treatment of Knee Osteoarthritis.
Official Title
Effect of Unloader Knee Brace and Biomechanical Footwear Device on Symptoms and Physical Function in Knee Osteoarthritis Patients - a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
December 2016 (Actual)
Primary Completion Date
October 2019 (Actual)
Study Completion Date
October 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Central Finland Hospital District

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study investigates the effects of unloader knee brace, biomechanical footwear device and exercise therapy on pain, physical function and quality of life in patients with knee osteoarthritis. The aim is to find more effective treatment strategies to delay or prevent heavy knee replacement surgeries.
Detailed Description
The aim of this study is to investigate the effects of exercising, and using a knee brace and exercising, and using of biomechanical footwear device on clinically important symptoms, physical function and quality of life in patients with osteoarthritis of the knee. The hypothesis is that the groups of using knee brace and biomechanical footwear can alleviate pain, improve physical function and quality of life more efficiently, than the group doing home exercises only. The subjects (n = 120) will be randomized into three groups mentioned above, after which they will start to do exercises, or to use a knee brace and do exercises, or to use biomechanical footwear at home according to the instructions for 4 months. Physical function, symptoms and quality of life will be measured before and after 4-month intervention. In addition, at 12-month time point follow-up surveys will be addressed with regard to symptoms and quality of life, as well as to cost-effectiveness of the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis,Knee
Keywords
Knee brace, biomechanical footwear, exercise, RCT

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise therapy group
Arm Type
Active Comparator
Arm Description
(n = 40)
Arm Title
Knee brace and exercise group
Arm Type
Experimental
Arm Description
(n = 40)
Arm Title
Footwear device group
Arm Type
Experimental
Arm Description
(n = 40)
Intervention Type
Other
Intervention Name(s)
Home-based exercise
Intervention Description
Home-based exercises three times per week.
Intervention Type
Device
Intervention Name(s)
Knee brace
Intervention Description
Progressive use of knee brace each day during activities of daily living.
Intervention Type
Device
Intervention Name(s)
Biomechanical footwear device
Intervention Description
Progressive use of footwear each day during activities of daily living.
Primary Outcome Measure Information:
Title
Change from baseline Pain intensity at 4 months: VAS
Description
Visual Analog Scale for Pain (score of 100 mm). No pain (score of 0), worst imaginable pain (score of 100).
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Change from baseline clinical symptoms at 4 months.
Description
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)-questionnaire evaluates the condition of patients with knee osteoarthritis including pain, stiffness and physical function. In the subscale of pain (score range 0 - 500), stiffness (score range 0 - 200), and functional limitation (score range 0 - 1700) lower values represent a better outcome. In order to normalize each score on 0 - 100 scales, the following correction factors are used: pain 0.20, stiffness 0.50, functional limitation 0.059.
Time Frame
4 months
Title
Change from baseline Health-Related Quality of Life at 4 months: SF-36
Description
The SF-36-Item Health Survey measures Health-Related Quality of Life. The SF-36 is a multi-item scale assessing eight health concepts: 1) limitations in physical activities, 2) limitations in social activities, 3) limitations in usual role activities, 4) bodily pain, 5) general mental health, 6) limitations in usual role activities, 7) vitality, and 8) general health perceptions, with scores for each dimensions ranging from 0 (poor health) to 100 (good health).
Time Frame
4 months
Title
Change from baseline isometric knee extension and flexion forces at 4 months.
Description
Will be measured with dynamometer
Time Frame
4 months
Title
Change from baseline walking speed gait parameter at 4 months.
Description
Walking speed (cm/sec) will be measured by the instrumented walkway system (GAITRite mat).
Time Frame
4 months
Title
Change from baseline cadence gait parameter at 4 months.
Description
Cadence (steps per minute) will be measured by the instrumented walkway system (GAITRite mat).
Time Frame
4 months
Title
Change from baseline stride length gait parameter at 4 months.
Description
Stride length, i.e., the distance between 2 successive placement of the same foot (cm) will be measured by the instrumented walkway system (GAITRite mat).
Time Frame
4 months
Title
Change from baseline step length gait parameter at 4 months.
Description
Step length, i.e., the distance measured from the heel point of one foot to the heel point of the other foot (cm) will be measured by the instrumented walkway system (GAITRite mat).
Time Frame
4 months
Title
Change from baseline stance time and % stance gait parameter at 4 months.
Description
Stance time (sec) and % stance will be measured by the instrumented walkway system (GAITRite mat).
Time Frame
4 months
Title
Change from baseline swing time and % swing gait parameter at 4 months.
Description
Swing time (sec) and % swing will be measured by the instrumented walkway system (GAITRite mat).
Time Frame
4 months
Title
Change from baseline 40 m Fast-paced Walk Test at 4 months.
Description
A fast-paced walking test that is timed over 4 x 10m for a total 40 m
Time Frame
4 months
Title
Change from baseline Stair Ascend/Descend Test at 4 months.
Description
The time (sec) it takes to ascend and descend a flight of stairs. The total time to ascend and descend steps (negative number indicates better performance) will be recorded and reported
Time Frame
4 months
Title
Change from baseline 30s Timed Chair Stand Test at 4 months.
Description
The maximum number of chair stand repetitions possible in a 30 second period. The total number of chair stands (up and down equals one stand) completed in 30 seconds will be reported.
Time Frame
4 months
Title
Change from baseline knee range of movement at 4 months.
Description
Will be measured with goniometer
Time Frame
4 months
Title
Change from baseline physical activity at 4 months.
Description
The short form of International Physical Activity (IPAQ-SF) questionnaire measures data on Health-Related Physical Activity. The IPAQ-SF Records the activity of four intensity levels (vigorous-intensity, moderate-intensity, walking, sitting) for the last 7 days. Results are reported as a continuous variable (MET minutes a week). To calculate MET minutes a week the MET value given (walking = 3.3, moderate activity = 4, vigorous activity = 8) is multiplied by the minutes the activity was carried out and again by the number of days that the activity was undertaken. To get total MET minutes of physical activity a week, the MET minutes achieved in each category are added together. Higher MET-values represent better outcome.
Time Frame
4 months
Title
Change from baseline cost-utility at 4 months.
Description
Will be measured with the items of the SF-6D questionnaire, which in turn can be converted from the items of the SF-36 questionnaire. The SF-6D score varies from 0 to 1, 0 representing worst health cost-utility and 1 best health utility.
Time Frame
4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: moderate or severe knee pain (>40mm on a VAS scale 0-100mm) radiographic knee osteoarthritis (Kellgren-Lawrence grades 1-3) age between 45 and 70 years Exclusion Criteria: inflammatory joint disease acute (<6 months) knee trauma arthroscopic surgery in the past six months a planned knee replacement surgery or other planned surgical treatment of the knee knee injections in the past 3 months superficial wounds at the knee area arterial insufficiency severe varicosities impaired vision postural difficulties body-mass index (BMI) >35kg/m2 fibromyalgia rheumatoid arthritis or other active rheumatoid inflammatory disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jari Ylinen, Ph.D., M.D.
Organizational Affiliation
Central Finland Hospital District
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Arja Häkkinen, Ph.D.
Organizational Affiliation
Central Finland Hospital District
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Konsta Pamilo, M.D.
Organizational Affiliation
Central Finland Hospital District
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ari Heinonen, Ph.D.
Organizational Affiliation
University of Jyväskylä, Finland
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Joost Dekker, Ph.D.
Organizational Affiliation
VU University Medical Center, Amsterdam, Netherlands
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Jari Arokoski, Ph.D, M.D.
Organizational Affiliation
University of Eastern Finland
Official's Role
Study Chair
Facility Information:
Facility Name
Central Finland Central Hospital
City
Jyväskylä
ZIP/Postal Code
40700
Country
Finland

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Knee Brace and Biomechanical Footwear in the Treatment of Knee Osteoarthritis.

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