RecruitingNot ApplicableNCT06409442

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

Effects of Corrective External Support and Regional Vibration Applications Added to the Rehabilitation Program in Subacromial Pain Syndrome: Randomized Controlled Study


Sponsor

Dokuz Eylul University

Enrollment

63 participants

Start Date

Jun 24, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests two treatments — a shoulder brace and vibration therapy — for people with shoulder impingement syndrome (pain and reduced movement caused by tendons being pinched in the shoulder). Researchers want to see which treatment works best and whether combining them helps. **You may be eligible if...** - You are over 18 years old - You have been diagnosed with subacromial shoulder impingement syndrome - You have had shoulder pain from this condition for at least 3 months - You have not received any shoulder treatment in the last 6 months - You can read and write Turkish **You may NOT be eligible if...** - You have had shoulder surgery or injury (other than impingement) requiring treatment in the past year - You received treatment for shoulder problems within the past 6 months Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERStandard Physiotherapy Program

Patients with Subacromial Impingement Syndrome (SIS) will receive a 6-week treatment program. Patients will be given a physiotherapy treatment program by a physiotherapist three times a week, and on the other days, patients will practice six selected simple exercises at home.

OTHERKinesio Taping

In addition to the standard physiotherapy program, kinesio taping (device) will be applied.

OTHERLocal Vibration Therapy

In addition to the standard physiotherapy program, local vibration (device) will be applied.


Locations(1)

Dokuz Eylül University

Izmir, Balçova, Turkey (Türkiye)

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NCT06409442


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