No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
University of Chicago · Other
Who this trial is looking for
This trial is looking for adults who are having knee replacement surgery. Participants will help researchers understand how their neighborhood’s resources and their recovery are connected, and whether monitoring their recovery remotely can lead to better outcomes.
Are You a Good Fit for This Trial?
You may be able to join if
I am over 18 years old.
I am having a knee replacement surgery with a smart implant or standard care.
You may not be able to join if
I have had knee or hip replacement surgery on the other leg within the last 90 days.
I have restrictions on weight-bearing after surgery or cannot participate in physical therapy.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 imp…
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).
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients over 18 years of age
* Patients undergoing unilateral primary or revision total knee arthroplasty with the smart knee implant or standard-of-care
Exclusion Criteria:
* Patients who receive contralateral knee replacement or contralateral or unilateral hip replacement…
Inclusion Criteria:
* Patients over 18 years of age
* Patients undergoing unilateral primary or revision total knee arthroplasty with the smart knee implant or standard-of-care
Exclusion Criteria:
* Patients who receive contralateral knee replacement or contralateral or unilateral hip replacement within 90 days before or after their knee replacement in this study
* Patients with post-operative weight-bearing restrictions or physical deconditioning prohibiting routine physical therapy participation
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