EFFECT OF NEUROMUSCULAR TRAINING ON SHOULDER FUNCTION
EFFECT OF NEUROMUSCULAR TRAINING ON SHOULDER FUNCTION IN PATIENTS WITH SHOULDER IMPINGEMENT SYNDROME: A DOUBLE BLINDED RANDOMIZED CONTROLLED TRIAL
研究概览
详细说明
Double-blinded randomized controlled trial (patient and research assistant (the examiner of all patients) will be blinded).
Participants:
Thirty-four patients of both genders will be selected through non-probability sampling diagnosed as Neer's stage II SIS and their age range from 25-45 years will be randomly assigned to 1 of 2 groups. Each patient will sign an informed consent before starting the study (Appendix III).
Eligible patients will be recruited by physical therapist via referral from the treating orthopedic surgeon who will diagnose SIS based on clinical and radiological examination.
Group I (control): it includes 17 patients who will receive traditional strength training program.
Group II (experimental): it includes 17 patients who will receive upper extremity neuromuscular training exercises
研究类型
注册 (预期的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名：aya ahmed nada, master degree
- 电话号码：+201285859034
- 邮箱：elnour653@gmail.com
研究联系人备份
- 姓名：maha mostafa mohammed, associate professor
- 电话号码：+201118803232
- 邮箱：maha.mostafa@pt.cu.edu.eg
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Patient age from 25-40 with a clinical diagnosis of Neer's stage II SIS (Consigliere et al., 2018).
Shoulder pain for at least three months (Heron et al., 2017) Painful arc of movement during flexion or abduction (Heron et al., 2017). Positive Neer's or Kennedy- Hawkins Test (Heron et al., 2017). Pain on resisted external rotation, abduction or Empty Can Test (Ager et al., 2019).
Exclusion Criteria:
Symptoms of cervical radiculopathy. Diagnosed inflammatory disorder. Neurological disorder. Widespread pain condition. Evidence of complete RC tear (positive drop arm test). Previous surgery to the affected shoulder.
:
学习计划
研究是如何设计的？
设计细节
- 主要用途：治疗
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：Group I (control)
: it includes 17 patients who will receive traditional strength training program.
|
traditional strength training exercises in group I
|
|
实验性的：Group II (experimental):
it includes 17 patients who will receive upper extremity neuromuscular training exercises
|
patients will receive neuromuscular training exercises in group II
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
SPADI (The Shoulder Pain and Disability Index)
大体时间：6 weeks
|
It is a self-report questionnaire for shoulder function
|
6 weeks
|
|
Inclinometer
大体时间：6 weeks
|
joint position sense
|
6 weeks
|
|
Hand held dynamometer
大体时间：6 weeks
|
isometric muscle strength
|
6 weeks
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (预期的)
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- shoulder neuromuscular
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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traditional training exerises的临床试验
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Karolinska InstitutetMinistry of Health and Social Affairs, Sweden完全的
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Mental Health Services in the Capital Region, DenmarkCopenhagen Trial Unit, Center for Clinical Intervention Research; Center for Clinical Intervention...完全的