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临床试验/NCT06349746
NCT06349746已完成不适用

The Addition of Cervical Unilateral Antero-posterior Mobilization and Thoracic Central Postro-anterior Mobilization to Selected Therapeutic Exercise Program in Treatment of Shoulder Impingement Syndrome: A Randomized Clinical Trial

Egyptian Chinese University1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2024年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
56
试验地点
1
主要终点
pain intensity

研究概览

简要总结

Shoulder impingement syndrome (SIS) is a complex, multi-factorial problem that is treated with a variety of different conservative options. The conservative option that has shown effectiveness is manual therapy of the cervical and thoracic spine

详细描述

This study will be conducted to answer the following question:

What is the effect of adding cervical and thoracic mobilization to selected therapeutic exercise Program on pain intensity, Pain-free shoulder flexion and scaption active ROM, muscle strength of external rotator and abductors, shoulder functional status in patients with Shoulder Impingement Syndrome

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 (Participant, Outcomes Assessor)

盲法说明

patients and outcomes assessor will be masked about the grouping of the study

入排标准

年龄范围
25 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • required at least three positive findings from five diagnostic tests for SIS (Hawkins-Kennedy test, Neer's test, painful arc, Resisted External Rotation test, Jobe's test) and persistent shoulder pain (anterolateral shoulder region) for 3 to 6 months, along with limitations in functional movements as Individuals who experienced painful restrictions in their ability to raise their shoulder (flexion, abduction, scaption) and had pain or limitations when performing functional movements such as reaching behind their back or behind their head. As well as subjects who willingly participated in the study and gave their consent for the research purposes.

排除标准

  • included adhesive capsulitis, radiologically confirmed grade III rotator cuff tears, calcific tendinitis, neurological or systemic disorders, cervical radiculopathy, prior shoulder surgery, recent corticosteroid injections, or recent physiotherapy within the previous three months. Patients complain from shoulder pain without pain on palpation, mobility limitations or pain during provocative tests, but complaining of abdominal tenderness on palpation were also excluded from this study.

研究组 & 干预措施

Therapeutic exercises

Active Comparator

a specific therapeutic exercise program consisted of stretching exercises for posterior capsule and progressive resistance exercises for rotator cuff and scapula stabilizer and home exercise

干预措施: therapeutic exercises (Other)

cervical and thoracic mobilization

Active Comparator

cervical unilateral antero-posterior mobilization and thoracic central postro-anterior mobilization added to therapeutic exercises

干预措施: mobilization exercise (Other)

结局指标

主要结局

pain intensity

时间窗: pre intervention and after 6 weeks of intervention

pain intensity will be measured by visual analogue scale

muscle strength

时间窗: pre intervention and after 6 weeks of intervention

shoulder flexors and external rotators muscle strength will be measured by dynamometer

shoulder flexion and abduction range of motion

时间窗: pre intervention and after 6 weeks of intervention

measurement of shoulder flexion and abduction range of motion applied by using digital goniometer

次要结局

未报告次要终点

研究者

发起方
Egyptian Chinese University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Noha Elserty

Assistant professor

Benha University

研究点 (1)

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