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Could your core strength affect your shoulder injury recovery?

NCT ID NCT07089628

Knowledge-focused Sponsor: Bandırma Onyedi Eylül University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This observational study will examine the relationship between core stability and reaction time, hand-eye coordination, pain, and function in 52 people with rotator cuff lesions, comparing them to healthy individuals. Participants will undergo various endurance and strength tests, as well as reaction time measurements using a light-based system. The goal is to understand if core stability plays a role in upper extremity function and motor performance in this population.

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 52 people

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

Started

Aug 2025

Expected to finish

Dec 2025

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

"Rotator cuff lesions are among the most common problems within musculoskeletal disorders. The prevalence of these lesions increases with age, and they encompass a wide spectrum of various injuries and pathological conditions. The literature frequently reports that these lesions often result in pain, reduced functional capacity, and a decline in quality of life. Although some of these lesions are traumatic in nature, the majority of rotator cuff issues are degenerative due to age-related changes in tendon structure.

Ages

18 to 65 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: * Having a diagnosis of a rotator cuff lesion confirmed by a physician * Having no history of any surgical procedure related to the shoulder * Experiencing activity-related pain scored as 3 or higher on the Visual Analog Scale Exclusion Criteria: * Presence of systemic inflammatory diseases * Pregnancy * Presence of mental health disorders * Individuals with communication difficulties * Presence of other significant shoulder pathologies such as dislocation, fracture, arthritis, or frozen shoulder * All of these criteria apply to the group with rotator cuff lesions. The other group consists of healthy, asymptomatic individuals.

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Conditions

The condition(s) this trial relates to.

Pain rotator cuff syndrome

As listed by the trial registrant

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

Core stability Core stabilization Function Pain Reaction time

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

  • Gazi University

    RECRUITING

    Ankara, Turkey (Türkiye)

More trials for these conditions

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