Knee Connect: Measuring Range of Motion and Gait Metrics After Total Knee Arthroplasty

Sponsor
Sunnybrook Health Sciences Centre (Other)
Overall Status
Completed
CT.gov ID
NCT03651739
Collaborator
(none)
51
1
14.3
3.6

Study Details

Study Description

Brief Summary

The main goals of total knee replacement (TKR) surgery are to relieve pain and to allow patients to remain active. Sunnybrook is working with Kineris Inc.to advance a wearable device, the Knee Connect, aimed at tracking the physical recovery of patients after total knee replacements. After surgery, patients experience a gradual progression in function as their knee range of motion (ROM) increases and their gait patterns normalize. Goals for these metrics are well documented after the patient is fully recovered. However, there is a lack of detailed information available about the week by week improvements patients make in these metrics. The main objective of this study is to determine the accuracy of the Knee Connect device in quantifying the weekly improvements in ROM and gait parameters of patients recovering from surgery.

Condition or Disease Intervention/Treatment Phase
  • Device: Knee Connect

Detailed Description

A research assistant will conduct in person data collections on 36 patients using the Kineris wearable device. The device is an electronic goniometer connected to a smart phone application. Patients will be recruited from the "Patient Orientation Program" (POP) at the Sunnybrook Holland Centre. Data collection will occur preoperatively, at the end of each physiotherapy Knee Class session, and at the three month postoperative clinic visit. The research assistant will help fit and attach the wearable device to each patient's knee. Patients will be asked to bend their knee (flexion and extension) while wearing the device which will measure patients range of motion. The research assistant will also measure knee range of motion using a handheld protractor. Afterward, patients will be asked to walk 10 steps, using any walking aids or techniques they typically use at home. There will be 15 collections per patient requiring ten minutes per session. Chart reviews will also be conducted to determine patient reported outcomes which will be then correlated with the functional measures.

All data will be extracted and input into an excel file. For both the ROM tests, the accuracy of the Knee Connect device will be compared against the plastic goniometer. This will be done by using a paired t-test and calculating interclass correlation coefficient. The data will then be analyzed using a repeated measures ANOVA and Bonferroni post-hoc analysis to determine differences in the variables week to week. Additionally, a regression analysis will be used to estimate the week by week improvements in these variables.

Study Design

Study Type:
Observational
Actual Enrollment :
51 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Knee Connect: Measuring Range of Motion and Gait Metrics After Total Knee Arthroplasty
Actual Study Start Date :
Oct 2, 2018
Actual Primary Completion Date :
Dec 11, 2019
Actual Study Completion Date :
Dec 11, 2019

Arms and Interventions

Arm Intervention/Treatment
TKR Patients

Any patient undergoing total knee arthroplasty and will use the Knee Connect during their knee classes at the Holland Centre

Device: Knee Connect
An electronic goniometer with smart phone application

Outcome Measures

Primary Outcome Measures

  1. Knee Range of Motion Error [One reading 2-4 weeks pre-operation, two readings weekly for 2-6 weeks post-operation (during physiotherapy knee class visits), one during 3 month post-operative clinic visit]

    The difference in measured knee range of motion (in degrees) between the Knee Connect and the handheld goniometer. Completed at each study time point (listed below) in order to gather as much data on the accuracy of knee connect compared to the goniometer.

Secondary Outcome Measures

  1. Knee range of motion [One reading 2-4 weeks pre-operation, two readings weekly for 2-6 weeks post-operation (during physiotherapy knee class visits), one during 3 month post-operative clinic visit]

    The weekly knee range of motion (in degrees) measured by the Knee Connect

  2. Stride Time [One reading 2-4 weeks pre-operation, two readings weekly for 2-6 weeks post-operation (during physiotherapy knee class visits), one during 3 month post-operative clinic visit]

    The weekly gait stride time (in seconds) measured by the Knee Connect

  3. Stance Range of Motion [One pre-operative, one during inpatient stay, 12 during knee class visits, one during 3 month clinic visit]

    The weekly gait stance range of motion (in degrees) measured by the Knee Connect

  4. Swing Range of Motion [One reading 2-4 weeks pre-operation, two readings weekly for 2-6 weeks post-operation (during physiotherapy knee class visits), one during 3 month post-operative clinic visit]

    The weekly gait swing range of motion (in degrees) measured by the Knee Connect

  5. Western Ontario and McMaster Universities Osteoarthritis Index [One at 6 week visit, one during 3 month clinic visit]

    Western Ontario and McMaster Universities Osteoarthritis Index function sub-scale and total score Sub scales: Pain (5 items, each rated on a scale from 0-4); Joint stiffness (2 items, each rated on a scale from 0-4), Physical function (17 items, each rated on a scale from 0-4 for level of difficulty) Score range: Pain subscale 0-20 WOMAC points; Joint stiffness subscale 0-8 WOMAC points. Physical function subscale 0-68 WOMAC points. Total score 0-96 WOMAC points (96 = worse pain, stiffness and physical function). Subscales are summed for total score

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Be currently on the waiting list for a primary TKR

  • Be enrolled for the "Knee Class" postoperative physiotherapy at the Sunnybrook Holland Centre with the expectation of attending the class through the duration of the class.

  • Be able to provide informed consent.

Exclusion Criteria:
  • Revision total knee arthroplasty

  • Neuromuscular disorder

  • Bilateral TKR procedures

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sunnybrook Holland Orthopaedic & Arthritic Centre Toronto Ontario Canada M4Y 1H1

Sponsors and Collaborators

  • Sunnybrook Health Sciences Centre

Investigators

  • Principal Investigator: David Wasserstein, MD, Sunnybrook Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Sunnybrook Health Sciences Centre
ClinicalTrials.gov Identifier:
NCT03651739
Other Study ID Numbers:
  • 02KINERIS2017
First Posted:
Aug 29, 2018
Last Update Posted:
Aug 18, 2020
Last Verified:
Aug 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Sunnybrook Health Sciences Centre

Study Results

No Results Posted as of Aug 18, 2020