NCT06861933Completed
The Effects of Scapulohumeral Rehabilitation on Scapula Kinematics and Upper Extremity Functionality in Individuals With Parkinson's Disease
The Effects of Scapulohumeral Rehabilitation on Scapula Kinematics and Upper Extremity Functionality in Individuals With Parkinson's Disease: A Single Blind Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 9 Oct 2026
Brief summary (registry, in English)
With this study, individuals diagnosed with PD in Burdur province in Turkey will be provided with a physiotherapy and rehabilitation program for the upper extremity, and it is thought that the treatment received by both groups will have a positive effect on the functionality of the individuals. According to the results of our study, it will be determined whether the scapula kinematics and upper extremity functionality of individuals diagnosed with PD are different from healthy individuals of the same age and gender. After the intervention programs applied to the individuals, it is thought that it will contribute to the physiotherapy and rehabilitation programs of individuals with PD by determining whether the scapulohumeral rehabilitation program is superior to the upper extremity neurorehabilitation program.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 28 (actual)
- First submitted
- 26 Feb 2025
- Start date
- Apr 2025
- Primary completion date
- Jan 2026
- Lead sponsor
- Burdur Mehmet Akif Ersoy University
- Diseases
- Parkinson disease
- NCT number
- NCT06861933
What you commit to
- Study type: Interventional
- Participants enrolled: 28
- From Apr 2025 to the primary completion date, Jan 2026
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- 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
- Failure to attend 3 consecutive sessions
Other
- Incomplete data
- Voluntary withdrawal
Who the study is looking for
- 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
Age in the registry: 40 years to 80 years · Sex: All · Accepts healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Burdur Mehmet Akif Ersoy University Coordinator of this site? Confirm its status | Burdur | Turkey (Türkiye) | Unknown status |
| Pamukkale University Coordinator of this site? Confirm its status | Denizli | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.