Effects of Corrective External Support and Regional Vibration Applications in Subacromial Pain Syndrome

Recruiting now · Not applicable

Conditions studied: Subacromial Pain Syndrome

In brief

Sixty three individuals with chronic subacromial pain syndrome will be included in our study. In the evaluations to be made to the participants; Pain intensity will be measured with the Visual Analogue Scale (VAS), joint movement and shoulder proprioception will be measured with the inclinometer, and shoulder muscle strength will be measured with the digital hand dynamometer. In addition, functionality and disability levels will be determined by SPADI and Short form-Questionnaire for Arm, Shoulder and Hand Problems (Q-DASH). Supraspinatus tendon thickness and acromiohumeral space measurements will be made by ultrasonographic imaging. Patient satisfaction will be evaluated with the Visual Analog Patient Satisfaction Scale survey and quality of life will be evaluated with the SF-12 survey (The 12-item Short Form Survey). Participants will be randomly divided into 3 groups of 21 participants each. In addition to the standard physiotherapy program, taping around the shoulder will be applied to the kinesio taping group, and localized vibration therapy around the shoulder will be applied to the localized vibration therapy group, in addition to the standard physiotherapy program. The Control Group (CG) will receive the same physiotherapy program as the other groups and will attend the same number of sessions as the other groups, accompanied by a physiotherapist. Evaluations will be made and analyzed before treatment, after 3 weeks of treatment, after 6 weeks of treatment, at 12 weeks and at the end of 24 weeks.

Key facts

Study ID: NCT06409442
Run by: Dokuz Eylul University
People needed: 63
Starts: 2024-06-24
Expected to finish: 2027-05-30
Last updated by the study team: 2026-06-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Volunteering to participate in the study,
Being over 18 years of age,
Having diagnosed with subacromial impingement syndrome,
SIS-related complaints have persisted for at least 3 months,
Not having received any treatment for shoulder problems in the last 6 months,
No history of shoulder injury other than subacromial impingement and/or shoulder symptoms requiring treatment for the last 1 year,
To be able to read and write Turkish in order to complete all evaluations and applications in the study and to carry out evaluations that require reading and writing.

You may not qualify if…

Having a history of fractures and surgery in the upper extremity and cervicothoracic region,
Having another neurological, orthopedic or rheumatic shoulder problem such as frozen shoulder or instability,
Having a systemic musculoskeletal disease,
Known chest deformity, scoliosis diagnosis and physical disability,
Presence of a skin problem or a condition that may be a contraindication to the application in the area where KT or LVT will be applied.

Where it is running

Dokuz Eylül University — Izmir, Balçova, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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