Early Versus Delayed Rehabilitation After Reverse Total Shoulder Arthroplasty for Proximal Humerus Fracture

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-85
SponsorUniversity of Virginia

About this trial

Proximal humerus fractures can be a debilitating injury in the elderly, impacting the ability to function independently or complete activities of daily living due to pain and restricted shoulder motion. Evidence has shown that reverse total shoulder arthroplasty (rTSA) is an effective option to improve pain and function for patients with acute displaced proximal humerus fractures. Given that patients undergoing rTSA for proximal humerus fractures typically experience worse functional outcomes, worse patient-reported outcomes, and higher rates of complication compared to those with elective indications for surgical intervention, it is critical to determine a secure path to recovery for these patients after surgery. Early rehabilitation has been proposed to be safe and effective for patients who undergo rTSA for elective indications; however, there is a paucity of research evaluating safety and effectiveness of timing of rehabilitation for rTSA patients in the trauma setting. Currently, there exists a great variability in postoperative rehabilitation protocols across orthopaedic practices. This study's objective is to determine the safety and effectiveness of early postoperative rehabilitation on the outcomes and postoperative complications of patients undergoing rTSA for proximal humerus fractures in order to provide more specific recommendations for this patient population.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

aged 50-85 undergo reverse Total Shoulder Arthroplasty by a single surgeon for proximal humerus fractures

Disqualifiers

previous rTSA to ipsilateral shoulder

undergoing elective rTSA

Prisoners

unwilling to be randomized

Trial design

Design model

Parallel

Treatments tested in this trial

  • Physical Therapy

    Other intervention

    Subjects will begin physical therapy at either 2 or 6 weeks s/p a rTSA.

Treatment groups

10 Participants
are divided into 2 treatment groups
Group A: Early Onset Physical TherapyActive comparator 1 intervention
Group B: Delayed Onset Physical TherapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Measurement of Range of motion of shoulder Forward Flexion using a goniometer

A goniometer will be used to measure forward flexion of the shoulder.

Time frame
2 week, 6 week, 3 month, and 6 month

Secondary outcomes

Other outcomes

Sponsors and contacts

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University of Virginia

Lead sponsor

Foundation of Orthopedic Trauma

Collaborator