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Shoulder injury may throw off your whole Body's balance, study finds

NCT ID NCT07636941

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at how rotator cuff injuries—common causes of shoulder pain—might affect posture, trunk rotation, and balance. Researchers will compare 40 people with rotator cuff problems to 40 healthy volunteers, measuring things like spine curvature and balance using smartphone apps and simple tests. The goal is to understand if shoulder issues are linked to broader body mechanics, which could improve rehabilitation approaches.

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 80 people

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

Started

Apr 2026

Expected to finish

Oct 2026

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 pathology (impingement syndrome, tendinopathy, or partial tear)

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 for rotator cuff pathology group: * Have been diagnosed with unilateral rotator cuff pathology (impingement syndrome, tendinopathy, or partial tear) by a specialist physician through clinical examination and/or radiological imaging (USG/MR); * have been between 18 and 65 years of age; have shoulder pain that has lasted for at least 3 months; * have a positive result on at least two of the Neer, Hawkins-Kennedy, and Empty Can tests; * have pain of at least 3/10 on the Pain Numerical Rating Scale (PMR) during rest or activity; * have sufficient cognitive ability to follow simple instructions and administer the tests; have a Mini Mental State Test score ≥24; * be able to provide signed informed consent and voluntarily agree to participate in the study. Inclusion Criteria for healthy group: * No history of shoulder, neck, or upper back injury and no painful symptoms reported in any of these areas within the last 12 months, * negative shoulder-specific tests (Neer, Hawkins, etc.), full range of motion on physical examination, and cognitive capacity to perform the tests. Exclusion Criteria: * Having undergone previous surgery in the shoulder or thoracic region; * Full-thickness rotator cuff tears requiring surgical indication; adhesive capsulitis, shoulder instability, labrum tears, or calcific tendinitis; * cervical radiculopathy or neurological diseases affecting the upper and lower extremities; * uncontrolled diabetes, inflammatory rheumatic diseases (rheumatoid arthritis, etc.), or malignancy; * severe osteoporosis in the thoracic region, structural scoliosis or advanced postural deformity that may affect trunk rotation, unstable vertebral fractures, or active infection; * having received steroid (cortisone) or PRP injections in the shoulder region within the last 3 months; * vestibular or visual impairment, those using medications that may affect balance, those with a lower extremity injury within the last 6 months.

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Conditions

The condition(s) this trial relates to.

Rotator Cuff Injuries rotator cuff syndrome

As listed by the trial registrant

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

Contacts and locations

Locations

  • Van Yüzüncü Yıl University

    Van, Tuşba, 65080, Turkey (Türkiye)

More trials for these conditions

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