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临床试验/NCT06156475
NCT06156475已完成不适用

The Effect of Electromyographic Biofeedback and Proprioception Exercises on Pain and Functionality in Patients With Subacromial Impingement Syndrome: A Randomized Controlled Study

Istanbul University - Cerrahpasa (IUC)1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2021年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
48
试验地点
1
主要终点
Disabilities of the Arm, Shoulder and Hand scale

研究概览

简要总结

The aim of this study is to investigate the effectiveness of Electromyographic Biofeedback with proprioception exercises on pain, range of motion, muscle strength, proprioception and functionality in patients with subacromial impingement syndrome.

详细描述

This study is planned as a prospective, randomized clinical study. Patients with subacromial impingement syndrome who volunteered to participate in the study, met the inclusion criteria, and signed the consent form were randomly assigned to the proprioception exercise group and the proprioception exercise with electromyographic biofeedback group. Demographic and clinical data of the patients were recorded. Shoulder function with Disabilities of the Arm, Shoulder and Hand scale, pain with VAS, painless active shoulder flexion, abduction, and external-internal rotation with goniometer, muscle strength with Manual Muscle Tester, proprioception (55°-90°- 125° angles of flexion and abduction, and angular deviations) with the Laser-pointer assisted angle reproduction test were evaluated, and patient satisfaction was evaluated with The Global Rating of Change Scale. After the initial evaluations were completed, only proprioception exercises and proprioception exercises with EMG-BF were applied 2 days a week for 8 weeks. Additionally, both groups were given Want exercises.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Being diagnosed with subacromial impingement syndrome,
  • Being between the ages of 18 and 65,
  • Not having received medical treatment,
  • Not having received a shoulder-related physiotherapy program in the last year,
  • Not having had any shoulder-related surgery,

排除标准

  • Neurological deficits of the upper extremity and the presence of another orthopedic disorder, rheumatic or congenital disease other than subacromial impingement syndrome,
  • Presence of mental problem,
  • Having received corticosteroid treatment in the last year,
  • Upper extremity fracture,
  • Acute cervical pathology,
  • Having cardiovascular and systemic diseases that prevent working,
  • Pregnancy,
  • Those with communication problems.

结局指标

主要结局

Disabilities of the Arm, Shoulder and Hand scale

时间窗: 8 weeks

The Disabilities of the Arm, Shoulder and Hand scale was used to measure shoulder function. The Disabilities of the Arm, Shoulder and Hand scale consists of 30 items. The total score that can be obtained from items scored between 1-5 varies between 0-100. An increase in the score indicates a decrease in function.

次要结局

  • Visual analogue scale(8 weeks)
  • Muscle strength(8 weeks)
  • Joint range of motion(8 weeks)
  • Proprioception(8 weeks)
  • Patient satisfaction(8 weeks)

研究者

发起方
Istanbul University - Cerrahpasa (IUC)
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ebru Kaya Mutlu, PT

Prof. Dr.

Istanbul University - Cerrahpasa (IUC)

研究点 (1)

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