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ENROLLING BY INVITATION
NCT06501859
NA

Rehabilitation With the Shoulder Pacemaker

Sponsor: University of Utah

View on ClinicalTrials.gov

Summary

The investigators purpose of the proposed study is to use the FDA approved Shoulder Pacemaker device in patients undergoing reverse shoulder arthroplasty and study the functional outcomes compared to a standard post-operative rehabilitation program. The investigators hypothesize that use of the Shoulder Pacemaker reduce pain and will allow for improved range of motion and function in patients undergoing RSA. The findings of this research may very well improve function in RSA patients through a novel, non-invasive approach.

Official title: Rehabilitation With the Shoulder Pacemaker After Reverse Shoulder Arthroplasty

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2023-08-02

Completion Date

2027-07

Last Updated

2025-10-29

Healthy Volunteers

No

Interventions

OTHER

Standard of care physical therapy

Standard rehabilitation protocol for 3 months.

DEVICE

Shoulder pacemaker with physical therapy

Standardized rehabilitation protocol with utilization of the shoulder pacemaker device 3 times per week over a 3-month period.

Locations (1)

University of Utah Orthopedics

Salt Lake City, Utah, United States