Heavy Slow Resistance Exercise for Subacromial Pain Syndrome
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 22
- 试验地点
- 2
- 主要终点
- Change from Baseline SPADI score at 12- and 24 weeks.
研究概览
简要总结
This study evaluates the effect of Heavy Slow Resistance exercise (HSR) exercise in comparison with traditional supervised exercise as treatment for patients with subacromial shoulder pain. The purpose is to evaluate if HSR is feasible fir these patients, and compare its effect to traditional exercise at pain and function of the shoulder. One half will complete the heavy slow resistance exercise, the other will complete the conventional exercise.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 25 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Shoulder pain > Three months
- •Subacromial pain
- •Dysfunction or pain during abduction
- •Pain during isometric strength test of abduction or external rotation of the shoulder.
- •Positive Hawkins test
- •Normal passive range of movement in the glenohumeral joint
排除标准
- •Surgery of the affected shoulder
- •Patients that are not considered suitable to complete the treatment, or able to answer a Norwegian questionnaire
- •Shoulder dislocation or shoulder instability
- •Clinical sign of cervical nerve root affection
- •Rheumatoid arthritis
- •Clinical sign of full rupture of the rotator cuff.
- •Pregnancy
- •Cortisone injection past six weeks
研究组 & 干预措施
Heavy slow resistance exercise
干预措施: Different exercise (Diagnostic Test)
Traditional supervised exercise
干预措施: Different exercise (Diagnostic Test)
结局指标
主要结局
Change from Baseline SPADI score at 12- and 24 weeks.
时间窗: Measured three times. Firstly at the baseline. Secondly at the 12-week follow up (after finished intervention). Lastly at the 24-week follow up.
The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities. The pain dimension consists of five questions regarding the severity of an individual's pain. Functional activities are assessed with eight questions designed to measure the degree of difficulty an individual has with various activities of daily living that require upper-extremity use. Both dimensions account for 50% of the overall score, and scores from 0 to 100.
次要结局
- Change from Baseline Active range of motion of the shoulder at 12- and 24 weeks.(Measured three times. Firstly at the baseline. Secondly at the 12-week follow up (after finished intervention). Lastly at the 24-week follow up.)
- Change from "The ability to take something down from a high shelf" score at 12- and 24 weeks.(Measured three times. Firstly at the baseline. Secondly at the 12-week follow up (after finished intervention). Lastly at the 24-week follow up.)
- Change from Baseline "Pain in rest last week" score at 12- and 24 weeks.(Measured three times. Firstly at the baseline. Secondly at the 12-week follow up (after finished intervention). Lastly at the 24-week follow up.)
- Change from Baseline "Pain in activity last week" score at 12- and 24 weeks.(Measured three times. Firstly at the baseline. Secondly at the 12-week follow up (after finished intervention). Lastly at the 24-week follow up.)
- Change From Baseline "The ability to carry a 5kg carry bag" score at 12- and 24 weeks.(Measured three times. Firstly at the baseline. Secondly at the 12-week follow up (after finished intervention). Lastly at the 24-week follow up.)
- Change from Baseline DASH score at 12- and 24 weeks.(Measured three times. Firstly at the baseline. Secondly at the 12-week follow up (after finished intervention). Lastly at the 24-week follow up.)
研究者
Hans-Hugo Fredriksen Høiland
Stud.med
Oslo University Hospital