RECRUITING

Investigating Patient Satisfaction With Smart Knee Implants

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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).

Official Title

Evaluating the Impact of Remote Therapeutic Monitoring on Knee Arthroplasty Recovery

Quick Facts

Study Start:2025-09-01
Study Completion:2027-10-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06968143

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients over 18 years of age
  2. * Patients undergoing unilateral primary or revision total knee arthroplasty with the smart knee implant or standard-of-care
  1. * Patients who receive contralateral knee replacement or contralateral or unilateral hip replacement within 90 days before or after their knee replacement in this study
  2. * Patients with post-operative weight-bearing restrictions or physical deconditioning prohibiting routine physical therapy participation

Contacts and Locations

Study Contact

Malik J Scott, BA
CONTACT
773-834-0822
mjscott1@uchicago.edu
Vincent Buckman, BS
CONTACT
vincent.buckman@uchicagomedicine.org

Principal Investigator

Sara Wallace, MD
PRINCIPAL_INVESTIGATOR
The University of Chicago Department of Orthopaedic Surgery

Study Locations (Sites)

The University of Chicago Medical Center
Chicago, Illinois, 60637
United States

Collaborators and Investigators

Sponsor: University of Chicago

  • Sara Wallace, MD, PRINCIPAL_INVESTIGATOR, The University of Chicago Department of Orthopaedic Surgery

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-09-01
Study Completion Date2027-10-31

Study Record Updates

Study Start Date2025-09-01
Study Completion Date2027-10-31

Terms related to this study

Keywords Provided by Researchers

  • Smart Knee Implant
  • Total Knee Arthroplasty
  • Remote Therapeutic Monitoring
  • Persona IQ

Additional Relevant MeSH Terms

  • Total Knee Arthroplasty
  • Knee Replacement
  • Knee Replacement Arthroplasty
  • Knee Osteoarthritis