MedTrace Logo

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

NCT05789784 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2026-01-05

No results posted yet for this study

Summary

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.

Conditions

  • Reverse Total Shoulder Arthroplasty
  • Physical Therapy

Interventions

OTHER

mymobility Physical Therapy

Physical therapy protocol administered at home through the mymobility application.

OTHER

Standard Office-based Physical Therapy

Physical Therapy protocol administered through exercise handouts and formal office-based therapy directed by physical therapist.

Sponsors & Collaborators

  • American Shoulder and Elbow Surgeons

    collaborator OTHER

  • Campbell Clinic

    lead OTHER

Principal Investigators

  • Tyler J Brolin, MD · Campbell Clinic

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-31
Primary Completion
2026-09-01
Completion
2027-03-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05789784 on ClinicalTrials.gov