Evaluating the Impact of Remote Therapeutic Monitoring on Knee Arthroplasty Recovery

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The main goal of this study is to see if there is a connection between the social and economic resources available in a patient's neighborhood (measured by the Area Deprivation Index, ADI) and their recovery after knee replacement surgery, as tracked through remote monitoring. A secondary goal is to find out if patients' self-reported pain and function score are linked to their actual physical improvement after surgery as measured by a remote therapeutic monitoring (RTM) device. Additionally, this study examines whether RTM can reduce the number of postoperative clinic visits within the first 90 days after surgery while maintaining patient satisfaction and patient-reported outcome measures (PROMs).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Patients over 18 years of age

• Patients undergoing unilateral primary or revision total knee arthroplasty with the smart knee implant or standard-of-care

Locations
United States
Illinois
The University of Chicago Medical Center
RECRUITING
Chicago
Contact Information
Primary
Malik J Scott, BA
mjscott1@uchicago.edu
773-834-0822
Backup
Vincent Buckman, BS
vincent.buckman@uchicagomedicine.org
Time Frame
Start Date: 2025-09-01
Estimated Completion Date: 2027-10-31
Participants
Target number of participants: 150
Treatments
Experimental: Smart Knee Implant
This group will receive the smart knee implant during their arthroplasty and will be able to track their progress according to the smart metrics through a mobile application, and will otherwise have the same standard-of-care as the other arm.
No_intervention: Standard-of-Care Knee Arthroplasty
This arm includes patients who are receiving the standard-of-care knee arthroplasty and will have standard follow-up with their surgeons.
Sponsors
Leads: University of Chicago

This content was sourced from clinicaltrials.gov