StepRite Evaluation
Primary Purpose
Osteoarthritis
Status
Terminated
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
StepRite
Sponsored by

About this trial
This is an interventional treatment trial for Osteoarthritis focused on measuring Total Knee Arthroplasty, Home monitoring
Eligibility Criteria
Inclusion Criteria:
- Unilateral total knee arthroplasty performed under regional (spinal +/- epidural) or general anesthesia. Surgical approach via an anterior 4-6 inch incision and utilizing a medial parapatellar arthrotomy incision. Posterior stabilized total knee arthroplasty decision.
- Age 55-75 yr. old
- BMI <35
Exclusion Criteria:
- History of neuromuscular disorder (e.g. Parkinson's, Polio, or stroke).
- Contralateral degenerative joint disease requiring a TKA.
- Pregnancy
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Device
Usual and customary care
Arm Description
Participants in this arm will receive the StepRite device. They will have a remote visit with their Physical Therapist in place of one in-person visit per week during the outpatient phase of their treatment
Participants in this arm will undergo usual care and will not be issued with the StepRite device
Outcomes
Primary Outcome Measures
Knee Osteoarthritis Outcome Score (KOOS)
The KOOS is a validated tool to measure pain and quality of life in patients after TKA
Secondary Outcome Measures
Full Information
NCT ID
NCT02270684
First Posted
October 17, 2014
Last Updated
April 1, 2017
Sponsor
University of Southern California
1. Study Identification
Unique Protocol Identification Number
NCT02270684
Brief Title
StepRite Evaluation
Official Title
Comparative Effectiveness of an Activity-Specific Monitoring Device (StepRite) on Short Term Outcomes in Adults After Total Knee Arthroplasty
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Terminated
Why Stopped
Recruitment and retention difficulties
Study Start Date
May 2015 (undefined)
Primary Completion Date
January 2016 (Actual)
Study Completion Date
January 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern California
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to compare the short-term changes in gait parameters and functional outcomes after total knee arthroplasty between those who use the StepRite device and those who follow a standard therapy program without the device.
Detailed Description
Total Knee Arthroplasty (TKA) is a procedure commonly used in severe degeneration of the knee joint due to osteoarthritis. With an increasing number of TKA's performed in a population that is aging during a time where the amount of healthcare dollars allotted to rehabilitation is declining, there is a need to develop remote monitoring of rehabilitation and to engage and optimize self-management of recovery.
Current management of TKA recovery is typically performed in the out-patient setting and is highly protocol driven. A typical case might be seen by the physical therapist 2-3x/week for 8-10 weeks to perform specific exercises and to monitor progress (i.e. compliance with range of motion (ROM) and strengthening exercises). One recent study suggested that variation in patients' independent exercise and activity after arthroplasty surgery may contribute to variable functional gains.
Telerehabilitation is an emerging method of delivering healthcare. It is likely to become more prevalent as technology improves and funding for clinic appointments diminishes. Recent studies have shown that telerehabilitation can be as effective as conventional treatment, as is well tolerated by both patients and healthcare professionals.
The StepRite system developed by MedHab (http://www.medhab.com/) allows the physical therapist to monitor physical activity and exercise remotely, thereby reducing the need for frequent out-patient visits. A thin insole placed inside the shoe measures foot contact pressure and a small device attached to the shoe measures acceleration. This information is translated into quantitative feedback about exercise compliance and performance measures comparing the surgical side with the non-surgical side. Real time feedback during exercise and weight-bearing activities is provided to the patient, and a HIPAA secured user interface website also displays this information in an online dashboard for both physical therapists and the physician.
Given the potential for improving patient engagement with rehabilitation, this study proposes a treatment model which includes monitoring activity outside of the clinic using the StepRite device and using a combination of outpatient appointments and remote consultations with therapists.
Hypothesis
Patients who use the device post-surgery will demonstrate superior short-term improvements (i.e. 6 months post TKA) with respect to self-reported functional outcomes and gait parameters, compared to a control group who does not use the device.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis
Keywords
Total Knee Arthroplasty, Home monitoring
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
4 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Device
Arm Type
Experimental
Arm Description
Participants in this arm will receive the StepRite device. They will have a remote visit with their Physical Therapist in place of one in-person visit per week during the outpatient phase of their treatment
Arm Title
Usual and customary care
Arm Type
No Intervention
Arm Description
Participants in this arm will undergo usual care and will not be issued with the StepRite device
Intervention Type
Device
Intervention Name(s)
StepRite
Intervention Description
The StepRite device uses an insole to monitor motion, and relays this information to the physical therapist via a smart phone app and web link. Set exercises can be programmed into the app for the participant to complete
Primary Outcome Measure Information:
Title
Knee Osteoarthritis Outcome Score (KOOS)
Description
The KOOS is a validated tool to measure pain and quality of life in patients after TKA
Time Frame
Baseline, 4, 10, 24 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Unilateral total knee arthroplasty performed under regional (spinal +/- epidural) or general anesthesia. Surgical approach via an anterior 4-6 inch incision and utilizing a medial parapatellar arthrotomy incision. Posterior stabilized total knee arthroplasty decision.
Age 55-75 yr. old
BMI <35
Exclusion Criteria:
History of neuromuscular disorder (e.g. Parkinson's, Polio, or stroke).
Contralateral degenerative joint disease requiring a TKA.
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher Powers, PhD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
12. IPD Sharing Statement
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StepRite Evaluation
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