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临床试验/NCT02100306
NCT02100306Unknown不适用

The Role of Auditory Feedback in Guiding Upper Extremity Movements

Sunnybrook Health Sciences Centre2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2014年5月最近更新:
适应症

试验速览

阶段
不适用
入组人数
26
试验地点
2
主要终点
Change in movement error from baseline

研究概览

简要总结

Stroke is one of the leading causes of disability, with an estimated prevalence of 50,000 cases per year in Canada. Less than half of stroke patients regain use of their arm and hand. There is currently no intervention regime that is the gold standard, despite the variety of therapeutic techniques used to treat the upper extremity post-stroke. The use of external feedback to improve motor learning is a technique that has been less studied but shows promise. Therefore, the purpose of this proof of principle study it to test whether different auditory feedback frequencies can facilitate reaching ability in people with stroke. In addition brain scans will be collected that will enable us to determine how stroke severity may impact on one's ability to improve with this technique.

We hypothesize that patients who receive less feedback (50% alternate) will have enhanced learning relative to the patients who receive more feedback (100%).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
30 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Unilateral first time MCA ischemic stroke
  • Stroke patients should have some movement of shoulder/elbow (no movement of hand - e.g. hand, fingers - is OK)
  • > 2 months post
  • between 30-85 years

排除标准

  • prior stroke
  • severe comprehension (or cognitive) deficit that compromises informed consent or understanding of instructions
  • contraindications to MRI (e.g. claustrophobia, metal implants)
  • neurodegenerative or psychiatric disease
  • auditory deficits that would impair testing
  • prior musculoskeletal injury to back or upper extremity (including shoulder subluxation from stroke)
  • skin conditions that would preclude taping of goniometers

结局指标

主要结局

Change in movement error from baseline

时间窗: participants will be followed for the duration of the study, an expected 3 hours per day for 2 weeks (5 days per week/10 days total)

次要结局

  • Change in range of motion(participants will be followed for the duration of the study, an expected 3 hours per day for 2 weeks (5 days per week/10 days total))
  • Change in movement duration(participants will be followed for the duration of the study, an expected 3 hours per day for 2 weeks (5 days per week/10 days total))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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