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Pre-Surgery workout may boost shoulder rotation after replacement

NCT ID NCT07145957

Symptom relief Sponsor: University of Florida Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether doing specific shoulder exercises for 6 weeks before reverse shoulder replacement surgery helps patients regain better internal rotation (the ability to reach behind the back). Researchers will compare range of motion, strength, and daily activities between a group that does pre-surgery exercises and a group that does not. The study involves 64 adults aged 40-80 who are scheduled for shoulder replacement due to arthritis or rotator cuff problems.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 64 people

The number the study aims to enrol. It can still change while the study runs.

Started

Nov 2025

Expected to finish

Sep 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Those patients who are indicated for primary reverse total shoulder arthroplasty with one of the attending surgeons on the study team that meet the inclusion/exclusion criteria will be approached by study team members to provide informed consent.

Ages

40 to 80 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: • Patients aged 40-80 * Undergoing primary RSA for glenohumeral osteoarthritis or rotator cuff arthropathy * Must be able to read and speak English * Willing and able to attend a monthly therapy session and perform exercises at home for a minimum of 6 weeks before surgery * Willing and able to participate in postoperative monitoring for a minimum of 2 years Exclusion Criteria: * Patients under the age of 40 and over the age of 80. * Diagnosis of septic shoulder, fracture, or fracture sequelae, or tumor pathology of the ipsilateral shoulder * Pre-existing hand, wrist, or elbow pathology that limits elbow flexion or extension, or forearm pronation or supination * Planned to undergo synchronous procedure of the involved extremity (e.g., synchronous RSA and carpal tunnel release) * Tendon transfer (e.g., Latissimus dorsi transfer) performed intraoperatively * Patients without access to phone or email communication for at least 2 years after treatment * Revision shoulder arthroplasty

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Conditions

The condition(s) this trial relates to.

arthropathy osteoarthritis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Primary reverse total shoulder arthroplasty

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • University of Florida Department of Orthopaedics and Rehabilitation

    RECRUITING

    Gainesville, Florida, 32607, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.