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Can shoulder exercises ease arm problems in Parkinson's?

NCT ID NCT06861933

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 26, 2026

Summary

This study tests whether a special shoulder rehabilitation program can improve arm and shoulder movement in people with Parkinson's disease. Twenty-eight participants will receive either the shoulder-focused rehab or a standard upper extremity program. The goal is to see if this approach helps with daily activities and reduces shoulder issues.

What this could mean

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

Active substance
Physiotherapy and rehabilitation (scapulohumeral rehabilitation)
What this could lead to
If successful, this could point toward a new physical therapy approach to improve arm and shoulder function in people with Parkinson's disease.
What could go wrong
This is a small, early-stage trial with only 28 participants, so results may not apply to everyone. The intervention is non-drug and relies on patient effort, which may limit effectiveness.

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

About 28 people

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

Started

Apr 2025

Expected to finish

Jun 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.

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: * For the intervention group: * Having been diagnosed with Parkinson's Disease * Being between 1-3 according to the Hoehn \& Yahr staging * For the control group: * Being of the same age and gender as the individuals diagnosed with Parkinson's disease included in the study Exclusion Criteria: * For the intervention group: * Refusing to participate in the study * Having a full-thickness rotator cuff muscle rupture * Having a history of humerus, clavicle, scapula or shoulder surgery * Having a history of humerus, clavicle, scapula or shoulder fracture * Having a history of any other disease that may affect the ability to stand independently * For the control group: * Refusing to participate in the study * Having a full-thickness rupture of the rotator cuff muscles * Having a history of humerus, clavicle, scapula or shoulder surgery * Having a history of humerus, clavicle, scapula or shoulder fracture Study Exclusion Criteria for Volunteers: * Failure to complete the tests included in the study * Failure to comply with the study schedule, failure to complete sessions * Incomplete data * Failure to attend 3 consecutive sessions * Voluntary withdrawal

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Burdur Mehmet Akif Ersoy University

    Burdur, Burdur, 15030, Turkey (Türkiye)

  • Pamukkale University

    Denizli, Denizli, 20200, Turkey (Türkiye)

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