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New treatment option for Subacromial Pain Syndrome
Official title Effects of Corrective External Support and Regional Vibration Applications in Subacromial Pain Syndrome
ClinicalTrials.gov ID: NCT06409442
What this study is testing
- What it's testing
- 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.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join 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,
You likely can't join 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.
See the full eligibility criteria
- 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.
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Izmir, Balçova, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Izmir, Balçova, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
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BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.