CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 51 enrolled
Drug / intervention
Knee Connectdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03651739
NCT03651739N/ACompleted

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

Sunnybrook Health Sciences Centre·observational·Posted Aug 29, 2018·Updated Aug 18, 2020

In Brief

An observational study evaluating Knee Connect for Arthroplasty, Replacement, Knee. Completed, enrolled 51 participants across 1 site.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesCanada
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedAug 29, 2018
Enrollment StartOct 2, 2018
Primary CompletionDec 11, 2019
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 7.8 years ago

Interventions

Knee Connectdevice

An electronic goniometer with smart phone application