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TracPatch in Total Knee Arthroplasty

Primary Purpose

Arthroplasty, Replacement, Knee, Osteoarthritis, Knee

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Consensus TracPatch
Sponsored by
University of Miami
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Arthroplasty, Replacement, Knee focused on measuring Wearable Technology, Total Knee Arthroplasty, Accelerometer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Surgical candidate for total knee arthroplasty
  • Greater than 18 years of age
  • Have signed the written informed consent form
  • Have consistent access to an iOS or Android device with Bluetooth capability

Exclusion Criteria:

  • Unwilling or unable to provide consent
  • Not fluent in the language of the informed consent form (English and Spanish)
  • Prisoners
  • Pregnant women
  • Wards of the state
  • Have previously undergone a TKA on that ipsilateral knee
  • Deformities of > 10 degrees valgus or varus or flexion contractures of > 10 degrees.
  • Considered by the surgeon to be a complex arthroplasty

Sites / Locations

  • University of Miami Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Wearable Technology Group

Current Standard of Care Group

Arm Description

Patients in this arm will be provided with their own Consensus TracPatch wearable device postoperatively and instructed on its use for six weeks.

Patients in this arm will not be provided with any wearable device. Participants will be evaluated as part of the study for a total of six weeks.

Outcomes

Primary Outcome Measures

Range of Motion
Range of motion, including flexion and extension of the knee will be measured with a goniometer in degrees. Measured in degrees, the patients range of motion in the operative knee will be measured before surgery and continuously by the TracPatch monitor up to six weeks post-operatively.

Secondary Outcome Measures

Patient-Reported Outcome Measurement Information System (PROMIS)
The PROMIS is a 10-question survey that assesses patient's overall functional status and ability to accomplish activities of daily living. It has a total score ranging from 9-55 with 9 indicating poor functional status.
Knee Injury and Osteoarthritis Outcome Score (KOOS Jr.)
The KOOS Jr. is a standardized scoring system developed to rate both the knee prosthesis function and the patient's functional abilities after total knee arthroplasty. It has a total score ranging from 0-100 with 0 indicating more severe symptoms.
Visual Analogue Score
A rating system from 1 - 10 developed to assess the patient's subjective rating of pain. A higher score indicates worse pain.

Full Information

First Posted
March 8, 2018
Last Updated
October 9, 2023
Sponsor
University of Miami
Collaborators
Consensus Orthopedics
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1. Study Identification

Unique Protocol Identification Number
NCT03466476
Brief Title
TracPatch in Total Knee Arthroplasty
Official Title
Evaluating the Efficacy of the TracPatch Wearable Technology on Patients Undergoing Total Knee Arthroplasty (TKA)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 20, 2017 (Actual)
Primary Completion Date
June 1, 2024 (Anticipated)
Study Completion Date
June 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Miami
Collaborators
Consensus Orthopedics

4. Oversight

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
Data Monitoring Committee
No

5. Study Description

Brief Summary
Total Knee Arthroplasty is becoming an increasingly common operation. An important part of a successful overall patient outcome is regaining functional range of motion after surgery. Wearable devices for fitness have become increasingly common. This study seeks to utilize wearable technology to enhance the post-operative rehabilitation experience by allowing patients and surgeons to monitor patient recovery in real time. The Consensus TracPatch is a wearable device which utilizes an accelerometer, temperature sensor and step count to monitor patient recovery. This tool provides critical, real-time information that may offer a more complete source of data to understand a patient's postoperative clinical and rehabilitation course and guide physician postoperative management. The study hypothesizes that this new technology will improve patient postoperative mobility and patient-physician communication.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arthroplasty, Replacement, Knee, Osteoarthritis, Knee
Keywords
Wearable Technology, Total Knee Arthroplasty, Accelerometer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients who meet enrollment criteria will be randomized to either the treatment group where they will receive their consensus tracpatch or be assigned to the control group where no wearable technology will be employed.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Wearable Technology Group
Arm Type
Experimental
Arm Description
Patients in this arm will be provided with their own Consensus TracPatch wearable device postoperatively and instructed on its use for six weeks.
Arm Title
Current Standard of Care Group
Arm Type
No Intervention
Arm Description
Patients in this arm will not be provided with any wearable device. Participants will be evaluated as part of the study for a total of six weeks.
Intervention Type
Device
Intervention Name(s)
Consensus TracPatch
Intervention Description
Consensus TracPatch will be attached to the participant's shin approximately two inches below the knee through use of an adhesive strip similar to a standard bandage for 6 weeks after total knee arthroplasty.
Primary Outcome Measure Information:
Title
Range of Motion
Description
Range of motion, including flexion and extension of the knee will be measured with a goniometer in degrees. Measured in degrees, the patients range of motion in the operative knee will be measured before surgery and continuously by the TracPatch monitor up to six weeks post-operatively.
Time Frame
Up to 6 weeks after surgery
Secondary Outcome Measure Information:
Title
Patient-Reported Outcome Measurement Information System (PROMIS)
Description
The PROMIS is a 10-question survey that assesses patient's overall functional status and ability to accomplish activities of daily living. It has a total score ranging from 9-55 with 9 indicating poor functional status.
Time Frame
Up to 6 weeks after surgery
Title
Knee Injury and Osteoarthritis Outcome Score (KOOS Jr.)
Description
The KOOS Jr. is a standardized scoring system developed to rate both the knee prosthesis function and the patient's functional abilities after total knee arthroplasty. It has a total score ranging from 0-100 with 0 indicating more severe symptoms.
Time Frame
Up to 6 weeks after surgery
Title
Visual Analogue Score
Description
A rating system from 1 - 10 developed to assess the patient's subjective rating of pain. A higher score indicates worse pain.
Time Frame
Up to 6 weeks after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Surgical candidate for total knee arthroplasty Greater than 18 years of age Have signed the written informed consent form Have consistent access to an iOS or Android device with Bluetooth capability Exclusion Criteria: Unwilling or unable to provide consent Not fluent in the language of the informed consent form (English and Spanish) Prisoners Pregnant women Wards of the state Have previously undergone a TKA on that ipsilateral knee Deformities of > 10 degrees valgus or varus or flexion contractures of > 10 degrees. Considered by the surgeon to be a complex arthroplasty
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Victor Hernandez
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Miami Hospital
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26842273
Citation
Belsi A, Papi E, McGregor AH. Impact of wearable technology on psychosocial factors of osteoarthritis management: a qualitative study. BMJ Open. 2016 Feb 3;6(2):e010064. doi: 10.1136/bmjopen-2015-010064.
Results Reference
background
PubMed Identifier
17589828
Citation
Kleijn LL, van Hemert WL, Meijers WG, Kester AD, Lisowski L, Grimm B, Heyligers IC. Functional improvement after unicompartmental knee replacement: a follow-up study with a performance based knee test. Knee Surg Sports Traumatol Arthrosc. 2007 Oct;15(10):1187-93. doi: 10.1007/s00167-007-0351-7. Epub 2007 Jun 23.
Results Reference
background
PubMed Identifier
24117351
Citation
Arosha Senanayake SM, Ahmed Malik O, Mohammad Iskandar P, Zaheer D. Assessing post-anterior cruciate ligament reconstruction ambulation using wireless wearable integrated sensors. J Med Eng Technol. 2013 Nov;37(8):498-510. doi: 10.3109/03091902.2013.837529. Epub 2013 Oct 14.
Results Reference
background
PubMed Identifier
25868424
Citation
Kwasnicki RM, Ali R, Jordan SJ, Atallah L, Leong JJ, Jones GG, Cobb J, Yang GZ, Darzi A. A wearable mobility assessment device for total knee replacement: A longitudinal feasibility study. Int J Surg. 2015 Jun;18:14-20. doi: 10.1016/j.ijsu.2015.04.032. Epub 2015 Apr 10.
Results Reference
background
Links:
URL
http://www.tracpatch.com/
Description
Device website available to public

Learn more about this trial

TracPatch in Total Knee Arthroplasty

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