Novel 3D Printed Knee Brace for Medial Knee Osteoarthritis
Primary Purpose
Osteoarthritis, Knee
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
KNEEMO knee brace
Popular knee brace
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis, Knee
Eligibility Criteria
Inclusion Criteria:
- Male or female aged between 40 and 70 years old having radiological and symptomatic medial KOA (Kellgren-Lawrence grade II, III or IV) according to the American College of Rheumatology's clinical and radiological criteria [83]
- Average knee pain > 4/10 (VAS score assessed three times in two weeks before being included)
- Not currently wearing knee brace
- Varus knee alignment equal or superior to 2°
- No or light pain from the hips, ankles, feet or lumbar spine
- Moderately physically active
- Able to understand written and spoken English.
Exclusion Criteria:
- Mild KOA (Kellgren-Lawrence grade I)
- Lateral or patellar KOA
- Chronic diseases or conditions (e.g., diabetes, osteoporosis, heart disease, hypertension, neurological disorders)
- Stroke history
- Inflammatory arthritis (gout, RA, psoriatic arthritis, …)
- Musculoskeletal disorders that could influence their ability to stand and walk
- Morbid obesity (BMI > 35)
- Intra-articular corticosteroid/hyaluronan injection in the affected knee in the past 3 months
- Unstable medication schedule and medication that causes dizziness
- Severe recent modification of diet
- Prosthetic implants in the hip, knee or ankle joint
- Poor skin condition
- Unable to walk, walk up and down stairs or any condition contraindicating the demands of the gait analysis.
Sites / Locations
- Glasgow Caledonian UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
KNEEMO knee brace & Popular knee brace
Popular knee brace &KNEEMO knee brace
Arm Description
Patients having medial knee osteoarthritis
Patients having medial knee osteoarthritis
Outcomes
Primary Outcome Measures
Change in knee pain during gait and stairs ambulation
Measured with 10-cm visual analog scale
Change in knee adduction moment during gait and stairs ambulation
Knee adduction moment (KAM) will be calculated from motion capture and force plate data. KAM characterizes knee loading, especially peaks and angular impulse (area under the KAM curve) to have information about maximum and total knee loading, respectively.
Secondary Outcome Measures
Change in knee brace comfort
Measured with 10-cm visual analog scale
Change in stability feelings
Measured with 10-cm visual analog scale
Change in Symptoms
KOOS questionnaires subscales
Change in quality of life
MOS SF-36 questionnaires subscales
Change in physical activities: Daily distance estimate
Measured (in km) during one week with an activity monitor.
Change in physical activities: Daily duration of sitting/standing/stair climbing
Measured in seconds during one week with an activity monitor.
Change in physical activities: Daily number of sitting/standing/stair climbing
Measured during one week with an activity monitor.
Change in physical activities: Weekly number of activities with moderate and high intensity
Measured during one week with an activity monitor.
Change in physical activities: Weekly duration of activities with moderate and high intensity
Measured in minutes during one week with an activity monitor.
Change in knee flexion moment during gait and stairs ambulation
Maximum knee flexion moment will be calculated from gait analysis data.
Change in duration of phases of gait and stairs ambulation
Measured in percentage of gait cycle from gait analysis data.
Change in step length of gait
Measured in meters from gait analysis data
Change in knee flexion/extension range of motion during gait and stairs ambulation
Measured during the gait cycle based on gait analysis data
Change in knee adduction/abduction range of motion during gait and stairs ambulation
Measured during the gait cycle based on gait analysis data
Full Information
NCT ID
NCT02873403
First Posted
July 27, 2016
Last Updated
March 1, 2017
Sponsor
Peacocks Medical Group
Collaborators
Glasgow Caledonian University, Westfälische Wilhelms-Universität Münster
1. Study Identification
Unique Protocol Identification Number
NCT02873403
Brief Title
Novel 3D Printed Knee Brace for Medial Knee Osteoarthritis
Official Title
A 3D Printed Knee Brace to Improve Symptoms, Biomechanics and Daily Life Among Medial Knee Osteoarthritis Patients
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 2017 (Anticipated)
Primary Completion Date
May 2017 (Anticipated)
Study Completion Date
June 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peacocks Medical Group
Collaborators
Glasgow Caledonian University, Westfälische Wilhelms-Universität Münster
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Around 250 millions of people in the world (3.8%) have knee osteoarthritis (KOA). Due to aging and increasing obesity, the prevalence of KOA is expected to increase in the developed country in the next 20 years. KOA decreases quality of life of patients through chronic pain, joint stiffness, and reduced social activity, which influence emotional wellness as well. KOA has also impact on the biomechanics of the lower limbs, leading or amplifying the tibiofemoral misalignment and an increase of the medial knee joint loading. Increase of the medial knee joint loading may lead patients into a vicious circle by increasing knee pain, decreasing activities, increasing weight and disease progression. Knee brace is a non-pharmacological treatment recommended for KOA. It aims to reduce misalignment of the limb. However, the main issue is the poor compliance because of lack of effectiveness, more drawbacks than benefits, discomfort, bad fitting, migration of the brace, bulkiness, aesthetic, skin irritation, blisters and too much pressure on the knee. By its freedom in design, 3D printing may resolve most of these complaints.
This study aims to compare clinical and biomechanical effectiveness, comfort and patients complaints of a knee brace made by 3D printing to a conventional knee brace.
The institute for Applied Health Research of Glasgow Caledonian University (GCU) will lead the experimental trial. They will recruit men or women (40 to 70 years old) suffering from medial KOA in Glasgow area. Participants will be in study for 10 weeks. During this period, they will wear 2 different knee braces for two weeks each with a 1-week period without knee brace between. Participants will have five visits to GCU: once for leg measurement to make knee braces and four times to fill questionnaires and perform gait analysis. Besides, they will wear activity monitor for 3 non-consecutive weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Knee
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
KNEEMO knee brace & Popular knee brace
Arm Type
Experimental
Arm Description
Patients having medial knee osteoarthritis
Arm Title
Popular knee brace &KNEEMO knee brace
Arm Type
Experimental
Arm Description
Patients having medial knee osteoarthritis
Intervention Type
Device
Intervention Name(s)
KNEEMO knee brace
Intervention Description
Bespoke knee brace made by additive manufacturing
Intervention Type
Device
Intervention Name(s)
Popular knee brace
Intervention Description
Customized knee brace used in the management of medial knee ostearthritis
Primary Outcome Measure Information:
Title
Change in knee pain during gait and stairs ambulation
Description
Measured with 10-cm visual analog scale
Time Frame
Baseline and at 2 weeks
Title
Change in knee adduction moment during gait and stairs ambulation
Description
Knee adduction moment (KAM) will be calculated from motion capture and force plate data. KAM characterizes knee loading, especially peaks and angular impulse (area under the KAM curve) to have information about maximum and total knee loading, respectively.
Time Frame
Baseline and at 2 weeks
Secondary Outcome Measure Information:
Title
Change in knee brace comfort
Description
Measured with 10-cm visual analog scale
Time Frame
Baseline and at 2 weeks
Title
Change in stability feelings
Description
Measured with 10-cm visual analog scale
Time Frame
Baseline and at 2 weeks
Title
Change in Symptoms
Description
KOOS questionnaires subscales
Time Frame
Baseline and at 2 weeks
Title
Change in quality of life
Description
MOS SF-36 questionnaires subscales
Time Frame
Baseline and at 2 weeks
Title
Change in physical activities: Daily distance estimate
Description
Measured (in km) during one week with an activity monitor.
Time Frame
Second week of intervention
Title
Change in physical activities: Daily duration of sitting/standing/stair climbing
Description
Measured in seconds during one week with an activity monitor.
Time Frame
Second week of intervention
Title
Change in physical activities: Daily number of sitting/standing/stair climbing
Description
Measured during one week with an activity monitor.
Time Frame
Second week of intervention
Title
Change in physical activities: Weekly number of activities with moderate and high intensity
Description
Measured during one week with an activity monitor.
Time Frame
Second week of intervention
Title
Change in physical activities: Weekly duration of activities with moderate and high intensity
Description
Measured in minutes during one week with an activity monitor.
Time Frame
Second week of intervention
Title
Change in knee flexion moment during gait and stairs ambulation
Description
Maximum knee flexion moment will be calculated from gait analysis data.
Time Frame
Baseline and at 2 weeks
Title
Change in duration of phases of gait and stairs ambulation
Description
Measured in percentage of gait cycle from gait analysis data.
Time Frame
Baseline and at 2 weeks
Title
Change in step length of gait
Description
Measured in meters from gait analysis data
Time Frame
Baseline and at 2 weeks
Title
Change in knee flexion/extension range of motion during gait and stairs ambulation
Description
Measured during the gait cycle based on gait analysis data
Time Frame
Baseline and at 2 weeks
Title
Change in knee adduction/abduction range of motion during gait and stairs ambulation
Description
Measured during the gait cycle based on gait analysis data
Time Frame
Baseline and at 2 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male or female aged between 40 and 70 years old having radiological and symptomatic medial KOA (Kellgren-Lawrence grade II, III or IV) according to the American College of Rheumatology's clinical and radiological criteria [83]
Average knee pain > 4/10 (VAS score assessed three times in two weeks before being included)
Not currently wearing knee brace
Varus knee alignment equal or superior to 2°
No or light pain from the hips, ankles, feet or lumbar spine
Moderately physically active
Able to understand written and spoken English.
Exclusion Criteria:
Mild KOA (Kellgren-Lawrence grade I)
Lateral or patellar KOA
Chronic diseases or conditions (e.g., diabetes, osteoporosis, heart disease, hypertension, neurological disorders)
Stroke history
Inflammatory arthritis (gout, RA, psoriatic arthritis, …)
Musculoskeletal disorders that could influence their ability to stand and walk
Morbid obesity (BMI > 35)
Intra-articular corticosteroid/hyaluronan injection in the affected knee in the past 3 months
Unstable medication schedule and medication that causes dizziness
Severe recent modification of diet
Prosthetic implants in the hip, knee or ankle joint
Poor skin condition
Unable to walk, walk up and down stairs or any condition contraindicating the demands of the gait analysis.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yoann Dessery, PhD
Email
yoann.dessery@peacocks.net
First Name & Middle Initial & Last Name or Official Title & Degree
Jari Pallari, PhD
Email
jari.pallari@peacocks.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yoann Dessery, PhD
Organizational Affiliation
Peacocks Medical Group
Official's Role
Principal Investigator
Facility Information:
Facility Name
Glasgow Caledonian University
City
Glasgow
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yoann Dessery, PhD
Email
yoann.dessery@peacocks.net
First Name & Middle Initial & Last Name & Degree
Yoann Dessery, PhD
12. IPD Sharing Statement
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Novel 3D Printed Knee Brace for Medial Knee Osteoarthritis
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