About this trial
Reverse total shoulder arthroplasty (RTSA) has been successful in patients with rotator cuff arthropathy, proximal humerus fractures, failed primary total shoulder arthroplasty or failed hemiarthroplasty, and massive irreparable rotator cuff tear. Patients who undergo an RTSA report pain relief and functional range of motion. It has been more than 20 years since the advent of the RTSA construct but an immediate post-operative rehabilitation with active shoulder range of motion has not been prospectively studied in comparison to the traditional post-operative rehabilitation highlighted by Boudreau et al.12 Investigators plan to prospectively follow our patients following RTSA undergoing an immediate active shoulder rehabilitation (IASR) vs traditional rehabilitation in a randomized controlled fashion. Investigators plan to document clinical outcomes, complications and cost effectiveness out to 1 year.
The study will hopefully fulfill the Triple Aim model for HealthPartners by improving the health of the population, improve the experience of each individual, and make healthcare affordable by decreasing the total cost of care.
Eligibility criteria
Qualifiers
> 55 years of age.
Candidate for a primary reverse total shoulder arthroplasty.
Capable of completing self-administered questionnaires.
Be willing and able to return for all study-related follow-up procedures.
Disqualifiers
Patients planning on undergoing a Primary Reverse Shoulder Total Arthroplasty due to proximal humeral fracture.
Previous shoulder surgery including previous total shoulder arthroplasty or reverse total shoulder arthroplasty or hemiarthroplasty, or instability repairs
Active bacterial infection of the shoulder.
Any concomitant shoulder procedure.
Trial design
Treatments tested in this trial
- Rehabilitiation
Treatment groups
Sponsors and collaborators
HealthPartners Institute
Lead sponsor
TRIA Orthopaedic Center
Collaborator