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临床试验/NCT05088668
NCT05088668暂停不适用

The Effectiveness of Augmented Reality Combined With Scapular Repositioning Exercises in Patients With Chronic Shoulder Pain and Scapular Dyskinesis: a Randomized Clinical Trial

Ruben Fernandez Matias2 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2021年10月27日最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
发起方
入组人数
52
试验地点
2
主要终点
Change in pain intensity

研究概览

简要总结

The aim of this study is to analyze whether an Augmented Reality based scapular stabilization exercise program is more effective than conventional programs in patients with chronic shoulder pain and Scapular Dyskinesis.

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 (Outcomes Assessor)

盲法说明

The researchers involved in measuring outcomes will not be aware of treatment allocation.

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Unilateral mechanical shoulder pain of nonspecific origin (non-traumatic) lasting at least 3 months.
  • Weakness in flexion, abduction and/or external rotation isometric strength testing.
  • Presence of scapular dyskinesis according to Kibler, Scapular Assistance Test, and Scapular Reposition Test.

排除标准

  • Previous shoulder surgery.
  • History of shoulder fracture or glenohumeral luxation.
  • History of acromioclavicular joint injury.
  • Presence of massive rotator cuff rears.
  • Presence of frozen shoulder.
  • Cervical hernias or radiculopathy.
  • Fibromyalgia.
  • Neuropathic pain.
  • Cervical and/or vestibular problems with dizziness, unsteadiness, or vertigo.
  • Medical contraindication for performing exercise (cardio-vascular or cardio-pulmonar diseases, systemic diseases, metabolic diseases in non-controlled acute state).
  • Blindness.
  • Actually being treated with physical therapy for shoulder pain.

结局指标

主要结局

Change in pain intensity

时间窗: Baseline, change from baseline at 1-month, change from baseline at 2-months, change from baseline at 3-months, and change from baseline at 6-months

Pain intensity measured with a visual analogue scale which ranges from 0 (no pain) to 10 (worst imaginable pain).

次要结局

  • Change in arm disability(Baseline, change from baseline at 1-month, change from baseline at 2-months, change from baseline at 3-months, and change from baseline at 6-months)
  • Change in shoulder disability(Baseline, change from baseline at 1-month, change from baseline at 2-months, change from baseline at 3-months, and change from baseline at 6-months)
  • Change in kinesiophobia(Baseline, change from baseline at 1-month, change from baseline at 2-months, change from baseline at 3-months, and change from baseline at 6-months)
  • Change in shoulder range of motion(Baseline, 1-month, 2-months, 3-months, and 6-months)
  • Change in catastrophism(Baseline, change from baseline at 1-month, change from baseline at 2-months, change from baseline at 3-months, and change from baseline at 6-months)
  • Change in surface electromiography(Baseline, change from baseline at 1-month, change from baseline at 2-months, change from baseline at 3-months, and change from baseline at 6-months)

研究者

发起方
Ruben Fernandez Matias
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ruben Fernandez Matias

Clinical Professor

University of Alcala

研究点 (2)

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