跳至主要内容
临床试验/NCT05479539
NCT05479539Unknown不适用

Effects of Action Observation Therapy in Patients Undergoing Surgery for Shoulder-instability

Istituto Clinico Humanitas0 个研究点目标入组 40 人开始时间: 2022年9月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
40
主要终点
Changes in shoulder function

研究概览

简要总结

The study will aim at investigating the effects of action observation therapy (action observation plus motor imagery) in patients with shoulder instability undergoing capsulo-plastic surgery. Forty subjects scheduled for capsulo-plastic surgery will be randomized into an AOT or Control group. AOT group will undergo action observation followed by motor imagery of upper limb motor tasks for 4 weeks after surgery, whereas Control group will perform no intervention. In addition, both groups will undergo postoperative usual care including immobilization with a brace and passive upper limb mobilization. All participants will be assessed for shoulder pain, function, range of motion, fear of movement and quality of life the day before surgery, at training end and 3 months after training end.

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 (Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Subjects undergoing capsule-plastic surgery or Latarjet stabilization for shoulder instability

排除标准

  • Previous upper limb surgery
  • Cognitive impairments
  • Visual or auditory impairments
  • Postoperative complications limiting upper limb motor recovery (e.g., infections)

结局指标

主要结局

Changes in shoulder function

时间窗: At baseline, after 4 weeks of training and at 3 month after the training end

Simple shoulder test

次要结局

  • Changes in shoulder pain(At baseline, after 4 weeks of training and at 3 month after the training end)
  • Changes in shoulder range of motion(At baseline, after 4 weeks of training and at 3 month after the training end)
  • Changes in fear of movement(At baseline, after 4 weeks of training and at 3 month after the training end)
  • Changes in quality of life(At baseline, after 4 weeks of training and at 3 month after the training end)

研究者

发起方
Istituto Clinico Humanitas
申办方类型
Other
责任方
Sponsor

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