Clinical Trial

Subscapularis Strength After Total Shoulder Arthroplasty

Study Description

Subscapularis Strength After Total Shoulder Arthroplasty

This is a randomized, double-blinded, standard of care-controlled clinical trial. The purpose of this study is to determine the difference in subscapularis strength and function after anatomic Total Shoulder Arthroplasty (aTSA) in patients who receive isolated subscapularis rehabilitation in addition to the standard rehabilitation after surgery at 12-month follow up. Specifically the investigators will measure subscapularis strength utilizing a dynamometer device and subscapularis function utilizing isolated subscapularis physical examination testing: belly-press, bear-hug, and lift-off tests. Additionally, investigators will document secondary outcome measures including shoulder range of motion and Patient Reported Outcome Measure Information System (PROMIS) questionnaire scores.

Location

Locations Selected Location

Methods

No pharmaceutical medication involved No pharmaceutical medication involved
Patients and healthy individuals accepted Patients and healthy individuals accepted

Procedure - Subscapularis Rehabilitation

Specific subscapularis rehabilitation exercises which are not included in the current, standard rehabilitation protocol assigned to total shoulder arthroplasty patients post-operatively.

Procedure - Standard Rehabilitation

Standard post-operative rehabiliation protocol assigned to all total shoulder arthroplasty patients postoperatively

Additional Information

Official Study Title

The Effect of Focused Rehabilitation on Subscapularis Strength After Total Shoulder Arthroplasty

Clinical Trial ID

NCT03854357

ParticipAid ID

bDkZAa