Apple watch study tests App-Based recovery for hip and knee surgery
NCT ID NCT03737149
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a mobile app (mymobility) paired with an Apple Watch can help people recover after hip or knee replacement surgery, possibly replacing standard physical therapy. Over 6,500 adults who were scheduled for joint replacement used the app for guided exercises and activity tracking. Researchers measured readmission rates and joint function scores to see if the digital approach works as well as traditional care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mymobility mobile app paired with Apple Watch
- What this could lead to
- If successful, this could show that a smartphone app and wearable device are a viable alternative to in-person physical therapy after joint replacement surgery.
- What could go wrong
- This is an observational study, not a treatment trial, so it cannot prove the app causes better outcomes. Results may not apply to all patients or healthcare settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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6,559 people
The number who actually took part.
- Started
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Oct 2018
- Finished
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Apr 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria 1. Subject must be 18 years of age or older. 2. Subject qualifies for a primary, unilateral total or partial knee arthroplasty, based on physical exam and medical history. 3. Investigator plans to treat subject with a commercially-available device, used on-label according to the manufacturer's instructions for use, as part of their clinical care. 4. Subject owns and maintains an iPhone capable of pairing to the Apple Watch, supporting iOS updates and is compatible with the mymobility App. 5. Subject is willing and able to complete the protocol required follow-up. 6. Subject is able to read and understand the language used in the mymobility App for their region. 7. Subject is willing and able to provide written Informed Consent and Authorization by signing and dating the IRB/EC approved Informed Consent Form and Authorization. Where applicable, subject must also be willing to provide authorization for use of protected health information in accordance with local privacy laws. 8. Subject is mobile with no more than a single cane/single crutch assist preoperatively. Exclusion Criteria 1. Subject is a current alcohol or drug abuser as defined by the investigator. 2. Subject is considered a member of a protected population (e.g., prisoner, mentally incompetent, etc.). 3. Subject has systemic inflammatory arthropathies which would interfere or compromise the activity profiles within this study. 4. Subject is currently participating in any other surgical intervention, physical therapy or pain management study which would compromise the results of this study. 5. Subject requires simultaneous or staged bilateral replacements, staged\<90 days apart. Subjects can be enrolled into the study for the second, staged arthroplasty if scheduled \>89 days after their first, contralateral replacement.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ascension Medical Group - University Orthopaedic Specialists
Rochester Hills, Michigan, 48307, United States
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Bluegrass Orthopaedics
Lexington, Kentucky, 40509, United States
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Cleveland Clinic Florida
Weston, Florida, 33331, United States
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Cleveland Clinic Main Campus
Cleveland, Ohio, 44195, United States
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Colorado Joint Replacement
Denver, Colorado, 80210, United States
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Duke University
Morrisville, North Carolina, 27560, United States
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Emory University
Atlanta, Georgia, 30329, United States
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Epworth Healthcare - Richmond
Richmond, Victoria, 3121, Australia
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Foundation for Orthopedic Research and Education
Temple Terrace, Florida, 33637, United States
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Hoag Orthopedic Institute
Irvine, California, 92618, United States
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JIS Orthopedics
New Albany, Ohio, 43054, United States
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Michigan Orthopaedic Surgeons
Troy, Michigan, 48084, United States
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Midwest Center for Joint Replacement
Indianapolis, Indiana, 46241, United States
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National Capital Private Hospital
Canberra, Australian Capital Territory, 2605, Australia
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New Mexico Orthopaedic Associates
Albuquerque, New Mexico, 87110, United States
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Newton-Wellesley Hospital
Newton, Massachusetts, 02462, United States
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OrthoBethesda
Bethesda, Maryland, 20817, United States
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Orthopedic + Fracture Specialists
Portland, Oregon, 97225, United States
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Panorama Orthopedics & Spine Center
Golden, Colorado, 80401, United States
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Policlinico Universitario Campus Bio-Medico
Roma, Italy
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ROC Orthopedics
Tualatin, Oregon, 97062, United States
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Rothman Institute
Montvale, New Jersey, 07645, United States
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Rothman Institute
Bryn Mawr, Pennsylvania, 19010, United States
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Rush University Medical Center
Chicago, Illinois, 60612, United States
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Sah Orthopaedic Associates
Fremont, California, 94538, United States
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St. Annaziekenhuis
Geldrop, Netherlands
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Stanford University
Redwood City, California, 94063, United States
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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
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University of Utah
Salt Lake City, Utah, 84108, United States
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Washington University
St Louis, Missouri, 63110, United States
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Other studies related to the condition(s) this trial covers.
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