Diagnosis and Treatment of Scapular Dyskinesis Combined With Impingement Syndrome of Shoulder
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 360
- 试验地点
- 2
- 主要终点
- visual analog pain scale (VAS)
研究概览
简要总结
The goal of this study is to diagnose scapular dyskinesis-which can appear as a cause or result of various shoulder disorders-through screening tests in patients with shoulder impingement syndrome, the most common shoulder condition. By identifying scapular dyskinesis, the study aims to maximize treatment outcomes through appropriate rehabilitative exercise therapy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- Triple (Participant, Care Provider, Outcomes Assessor)
盲法说明
The investigators plan to enroll patients who consent to participate in the study and allocate them into two groups using a random sequence generator. A random allocation table will be created and managed by a third party who is not involved in the study. When planning the treatment method, group assignment will be requested from this third party holding the allocation table, ensuring that the allocator is blinded to the upcoming group assignments in advance. Treatment in each group will be administered consistently according to a pre-agreed protocol, and follow-up will also be conducted using the same method in both groups.
入排标准
- 年龄范围
- 20 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Inclusion Criteria
- •Patients diagnosed with unilateral shoulder impingement syndrome in the outpatient clinic (based on clinical symptoms and MRI) from the IRB approval date until March 1, 2027
- •Individuals who provided written informed consent after receiving a thorough explanation of the study prior to any procedures
- •Age 20 years or older
排除标准
- •Individuals who did not receive a subacromial steroid injection for shoulder impingement syndrome
- •Individuals with a history of surgical treatment or fracture in the affected shoulder
- •Individuals who refused to participate in the study
- •Individuals with neurological disorders affecting the ipsilateral upper extremity
结局指标
主要结局
visual analog pain scale (VAS)
时间窗: Initial, 3, 7, 13 weeks
0-10, 0: not satisfied, 10: very much satisfied
次要结局
- American Shoulder and Elbow Surgeons' (ASES) score(Initial, 3, 7,13 weeks)
- Constant score(Initial, 3, 7, 13 weeks)
研究者
Jung-Taek Hwang
Professor
Chuncheon Sacred Heart Hospital