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New rehab approach aims to get shoulder surgery patients back to daily life faster

NCT ID NCT07665541

Symptom relief Sponsor: Medipol University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 18, 2026 · Updated 2 times

Summary

This study compares task-oriented occupational therapy to standard rehab for people recovering from rotator cuff surgery. Thirty participants will be randomly assigned to one of two groups, attending 40-minute sessions twice a week for 10 weeks. The goal is to see if focusing on meaningful daily activities improves performance and satisfaction more than conventional exercises.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
task-oriented occupational therapy
What this could lead to
If it works, this could point toward a more effective rehab approach that helps people return to meaningful daily activities faster after rotator cuff surgery.
What could go wrong
This is a small, early-stage trial with only 30 participants, so results may not apply to everyone. The therapy is behavioral, so benefits depend on individual effort and adherence.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

14 people

The number who actually took part.

Started

Aug 2026

Finished

Aug 2026

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.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Individuals aged 18 years and older * Individuals who have undergone rotator cuff surgery * Medically stable and cleared for participation in a rehabilitation program * Ability to understand and follow instructions * Voluntary agreement to participate in the study Exclusion Criteria: * \- Presence of severe neurological disorders affecting upper extremity function * Severe cognitive impairment limiting participation * Additional musculoskeletal conditions affecting the upper extremity * Postoperative complications that may interfere with rehabilitation * Participation in another rehabilitation program during the study period

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Conditions

The condition(s) this trial relates to.

rotator cuff syndrome

As listed by the trial registrant

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

Rotator cuff tear repair

Contacts and locations

Locations

  • Istanbul Medipol University

    Istanbul, Istanbul, 34815, Turkey (Türkiye)

More trials for these conditions

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