Smart Kneebrace for Continuous Monitoring of Joint Angles During Rehabilitation
Primary Purpose
Arthroplasty, Replacement, Knee, Knee Osteoarthritis
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Smart Kneebrace with a smart phone app
regular rehabilitation procedure
Sponsored by
About this trial
This is an interventional treatment trial for Arthroplasty, Replacement, Knee focused on measuring total knee arthroplasty, rehabilitation, Smart Kneebrace
Eligibility Criteria
Inclusion Criteria:
- Ready to receive single-side TKA
Exclusion Criteria:
- contraindication of surgery
- self-reported diseases that cause lower limb disability (for example, cerebrovascular disease especially stroke)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Smart Kneebrace
without Smart Kneebrace
Arm Description
Smart Kneebrace with a smart phone app will be used during the rehabilitation after surgery for three months
regular rehabilitation procedure will be applied after surgery
Outcomes
Primary Outcome Measures
The change of postoperative joint angles
Patients in both groups will wear the smart kneebrace by which the range of motion of the knee joint can be calculated.
Secondary Outcome Measures
The change of knee pain.
Visual Analogue Scale of pain is a scale to extimate pain, and its score ranges from 0 to 10. The higher the score is, the more severe pain the patient is feeling.
The change of knee symptoms.
The Western Ontario and McMaster Universities Osteoarthritis Index(WOMAC),and its score ranges from 0 to 96. The higher the score is, the more severe symptoms the patient is feeling.
Full Information
NCT ID
NCT03365284
First Posted
November 25, 2017
Last Updated
December 2, 2017
Sponsor
Peking University People's Hospital
Collaborators
Peking University
1. Study Identification
Unique Protocol Identification Number
NCT03365284
Brief Title
Smart Kneebrace for Continuous Monitoring of Joint Angles During Rehabilitation
Official Title
Smart Kneebrace for Continuous Monitoring of Joint Angles During Rehabilitation After Total Knee Arthroplasty
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2018 (Anticipated)
Primary Completion Date
December 31, 2019 (Anticipated)
Study Completion Date
December 31, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University People's Hospital
Collaborators
Peking University
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
This study aims to investigate the effect of Smart Kneebrace use for osteoarthritis patients after total knee arhtroplasty (TKA) on post-operative performance.
Detailed Description
This is a single-center, open-label randomized controlled clinical trail. A total of 60 participants will receive total knee arthroplasty, who will be randomly assigned into experiment or control group. Smart Kneebrace will be used for the patients during the rehabilitation for the patients in experiment group, while the patients in the control group will not receive such a smart kneebrace. Postoperative joint angles as well as visual analog scale pain score, the Western Ontario and McMaster Universities Osteoarthritis Index knee society score will be estimated before operation and at 6/12 weeks after operation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arthroplasty, Replacement, Knee, Knee Osteoarthritis
Keywords
total knee arthroplasty, rehabilitation, Smart Kneebrace
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Smart Kneebrace
Arm Type
Experimental
Arm Description
Smart Kneebrace with a smart phone app will be used during the rehabilitation after surgery for three months
Arm Title
without Smart Kneebrace
Arm Type
Placebo Comparator
Arm Description
regular rehabilitation procedure will be applied after surgery
Intervention Type
Device
Intervention Name(s)
Smart Kneebrace with a smart phone app
Intervention Description
Smart Kneebrace will be used during the rehabilitation. Patients wearing the Smart KneeBrace are able to know their daily activity summary and exercise performance during rehabilitation training through a smart phone app.
Intervention Type
Other
Intervention Name(s)
regular rehabilitation procedure
Intervention Description
regular rehabilitation procedure, especially muscle strengthening exercises
Primary Outcome Measure Information:
Title
The change of postoperative joint angles
Description
Patients in both groups will wear the smart kneebrace by which the range of motion of the knee joint can be calculated.
Time Frame
before operation and 6/12 weeks after operation
Secondary Outcome Measure Information:
Title
The change of knee pain.
Description
Visual Analogue Scale of pain is a scale to extimate pain, and its score ranges from 0 to 10. The higher the score is, the more severe pain the patient is feeling.
Time Frame
before operation and 6/12 weeks after operation
Title
The change of knee symptoms.
Description
The Western Ontario and McMaster Universities Osteoarthritis Index(WOMAC),and its score ranges from 0 to 96. The higher the score is, the more severe symptoms the patient is feeling.
Time Frame
before operation and 6/12 weeks after operation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Ready to receive single-side TKA
Exclusion Criteria:
contraindication of surgery
self-reported diseases that cause lower limb disability (for example, cerebrovascular disease especially stroke)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhiwei Zhou
Phone
+8613521817377
Email
zzwwwdz@sina.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jianhao Lin, MD
Organizational Affiliation
Arthritis clinic and research center, Peking University Peoples' Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
22520559
Citation
Patel S, Park H, Bonato P, Chan L, Rodgers M. A review of wearable sensors and systems with application in rehabilitation. J Neuroeng Rehabil. 2012 Apr 20;9:21. doi: 10.1186/1743-0003-9-21.
Results Reference
background
PubMed Identifier
25311517
Citation
Sosdian L, Dobson F, Wrigley TV, Paterson K, Bennell K, Dowsey M, Choong P, Allison K, Hinman RS. Longitudinal changes in knee kinematics and moments following knee arthroplasty: a systematic review. Knee. 2014 Dec;21(6):994-1008. doi: 10.1016/j.knee.2014.09.009. Epub 2014 Oct 12.
Results Reference
background
PubMed Identifier
23554153
Citation
Mills K, Hunt MA, Ferber R. Biomechanical deviations during level walking associated with knee osteoarthritis: a systematic review and meta-analysis. Arthritis Care Res (Hoboken). 2013 Oct;65(10):1643-65. doi: 10.1002/acr.22015.
Results Reference
background
PubMed Identifier
22867935
Citation
Brostrom EW, Esbjornsson AC, von Heideken J, Iversen MD. Gait deviations in individuals with inflammatory joint diseases and osteoarthritis and the usage of three-dimensional gait analysis. Best Pract Res Clin Rheumatol. 2012 Jun;26(3):409-22. doi: 10.1016/j.berh.2012.05.007.
Results Reference
background
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Smart Kneebrace for Continuous Monitoring of Joint Angles During Rehabilitation
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