Study of Zimmer Biomet Mymobility Application on Reverse Total Shoulder Arthroplasty (RTSA) Outcomes

Enrolling by invitation · Not applicable

Conditions studied: Reverse Total Shoulder Arthroplasty, Physical Therapy

In brief

This is a trial comparing self-directed rehabilitation using the Zimmer Biomet mymobility digital platform versus standard office-based physical therapy after reverse shoulder replacement. The investigators hypothesize that there will be no difference in the postoperative outcomes between the mymobility cohort and the standard office-based physical therapy cohort.

Key facts

Study ID

NCT05789784

Run by

Campbell Clinic

People needed

100

Starts

2023-10-31

Expected to finish

2027-03-31

Last updated by the study team

2026-01-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 years of age or older.
• Primary Reverse Total Shoulder Arthroplasty performed for diagnosis of cuff tear arthropathy (CTA), massive rotator cuff tears (mRCT), osteoarthritis (OA), or inflammatory arthritis (IA).
• Have a functioning smartphone model compatible with the mymobility platform.

You may not qualify if…

• Less than 18 years of age.
• Revision Reverse Total Shoulder Arthroplasty
• Concomitant tendon transfer
• Planned discharge to inpatient rehab facility, skilled nursing home, or use of home health therapy

Where it is running

• Atlantis Orthopedics — Palm Beach Gardens, Florida, United States
• Ohio State University Medical Center — Columbus, Ohio, United States
• Rothman Orthopaedic Institute — Philadelphia, Pennsylvania, United States
• Campbell Clinic — Germantown, Tennessee, United States

Full record on ClinicalTrials.gov

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