Comparing early and delayed rehabilitation after shoulder surgery for fractures

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effects of early versus delayed rehabilitation on patients who undergo reverse total shoulder arthroplasty (rTSA) for proximal humerus fractures. It is a randomized controlled trial where participants will be assigned to start physical rehabilitation either two weeks or six weeks after surgery. The primary focus is to assess differences in range of motion, patient-reported outcomes, and postoperative complications between the two groups. The study aims to provide insights into the optimal timing for rehabilitation to enhance recovery in this patient population.

Why it matters

Who can join: the full rules

Inclusion Criteria:

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

Exclusion Criteria:

* previous rTSA to ipsilateral shoulder
* undergoing elective rTSA
* Prisoners
* unwilling to be randomized
* unwilling or unable to attend follow up visits

Where it's running

• University of Virginia Medical Center
  Charlottesville, Virginia, United States Recruiting

Study contacts

• Principal investigator: Seth Yarboro, MD — University of Virginia
• Study coordinator: Lori Elder
• Email: LJE5U@uvahealth.org
• Phone: 434-924-8570

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.