About this trial

The purpose of this study is to evaluate compare postoperative range of motion in patients who are given a sling for comfort only and allowed to start early active range of motion compared to patients who are placed in a sling for 4 weeks with passive range of motion only. Once enrolled, the patients will be randomized through computer randomization then placed in paper packets into either the immobilization group or the early range of motion group.

Eligibility criteria

Qualifiers

Patients 60 years or older who have a displaced proximal humerus fracture

Meets surgical criteria for a reverse total shoulder arthroplasty

Receive surgical intervention within 6 weeks of initial injury

Disqualifiers

Patients <60 years in age

Patients who cannot undergo surgery due to medical comorbidities

Patients who receive surgical intervention after 6 weeks from initial injury

Patients who have preoperative nerve damage from their fractures that would limit the ability to move the arm postoperatively

Trial design

Treatments tested in this trial

  • Early Range of Motion
  • Immobilization

Treatment groups

40 Participants
are divided into 2 treatment groups

Locations

1
Cooper University Hospital08103, CamdenNew Jersey, United States

Sponsors and collaborators

The Cooper Health System

Lead sponsor