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临床试验/NCT07228455
NCT07228455已完成不适用

The Effect of Humeral Head Depressor Strengthening in Individuals With Subacromial Impingement Syndrome

Near East University, Turkey1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年7月3日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
Acromio-humeral Distance (Ultrasonography, USG)

研究概览

简要总结

Subacromial impingement syndrome is a common musculoskeletal disorder. Therefore, to improve the shoulder biomechanics affected by the syndrome, an intervention group was compared with a control group. The exercise program applied to the intervention group is expected to improve the function of the shoulder complex.

详细描述

Subacromial Impingement Syndrome (SIS) is one of the most common musculoskeletal problems in the shoulder joint. This study aimed to investigate the effectiveness of a rehabilitation program targeting humeral head depressor muscles on symptoms in individuals with SIS.Participants were randomly divided into study and control groups.Volunteers who complained of shoulder pain for more than a month, who had limitation in passive movement compared to the other side shoulder, who had Neer impingement test, Hawkins test, Jobe supraspinatus test, and who were able to com-municate were included in the study. Individuals 1) Having any neurological condition affecting the upper extremity, 2) having neurological findings related to cervical disc herniation, 3) having a full-thickness rupture of one of the rotator cuff tendons, 4) having calcific tendonitis, 5) having undergone previous shoulder surgery and 6) Physical therapy-rehabilitation for the shoulder with the same complaints in the last 6 months, or 7) receiving corticosteroid injection were excluded from the study. While the control group received standard physical therapy and rehabilitation, the study group underwent a progressive resistance exercise program to strengthen the humeral head depressors and peri-articular muscles, including the rotator cuff. Acromio-humeral distance (AHD) and tendon thickness measurements were evaluated by ultrasonography, while pain intensity was measured through VAS and McGill Questionnaire, upper extremity disability through DASH-T, and kinesiophobia through Fear Avoidance Beliefs Questionnaire, respectively.

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)

盲法说明

Participants were blinded to their group assignment, but therapist were aware of the group allocations

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

  • Volunteers who complained of shoulder pain for more than a month,
  • Who had limitation in passive movement compared to the other side shoulder,
  • Who had Neer impingement test, Hawkins test, Jobe supraspinatus test, and -
  • Who were able to com-municate were included in the study

排除标准

  • Having any neurological condition affecting the upper extremity,
  • Having neuro-logical findings related to cervical disc herniation,
  • Having a full-thickness rupture of one of the rotator cuff tendons,
  • Having calcific tendonitis,
  • Having undergone previous shoulder surgery,
  • Physical therapy-rehabilitation for the shoulder with the same complaints in the last 6 months,
  • Receiving corticosteroid injection were excluded from the study

结局指标

主要结局

Acromio-humeral Distance (Ultrasonography, USG)

时间窗: Baseline and 6 weeks

次要结局

  • Tendon Thickness Measurment(Baseline and 6 week)
  • Pain (Visual Analog Scale, VAS)(Baseline and 6 weeks)
  • Pain (McGill Pain Questionnaire-Pain Rating Index)(Baseline and 6 weeks)
  • Kinesiophobia (Fear Avoidance Beliefs Questionnaire - FABQ, Physical Activity subscale)(Baseline and 6 weeks)
  • Kinesiophobia (Fear Avoidance Beliefs Questionnaire - FABQ, Work subscale)(Baseline and 6 weeks.)
  • Upper Extremity Disability Through (DASH-T)(Baseline and 6 weeks)

研究者

发起方
Near East University, Turkey
申办方类型
Other
责任方
Principal Investigator
主要研究者

Utku Kurtaran

Principal Investigator

Near East University, Turkey

研究点 (1)

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