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临床试验/NCT06892886
NCT06892886招募中不适用

Using Immersive Virtual Reality for the Upper Limb Rehabilitation of Post-stroke Subjects: a Multicenter Randomized Control Trial

University Hospital of Ferrara2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2023年3月1日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
48
试验地点
2
主要终点
Changes in upper limb impairment

研究概览

简要总结

Stroke produces brain damages that results in sensory, motor, and cognitive impairments which reduce the patient's quality of life and social participation. Upper limb recovery is a complex process whose goal is to allow the patients to gain, in part or completely, independence in daily living activities, for that it represents one of the most important rehabilitation focus. Virtual reality is a fairly recent approach able to simulate concrete movements and functional tasks in a higher dosage compared to other therapies. It seems that the use of VR could improve limb function, however, the amount of this gain is still unclear because of insufficient evidence. This study aims at quantitatively investigating the effectiveness of an HMD immersive virtual reality system on the upper limb functioning in subacute stroke survivors.

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)

盲法说明

The randomization scheme will be generated using the website http://www.randomization.com and managed by an external administrator. The clinicians who will perform the outcome assessment will be blind regarding the subject's group.

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • diagnosis of first, ischemic or hemorrhagic, stroke verified by brain imaging within 4 week
  • upper limb motor impairment defined by an upper extremity score <55 on the Fugl-Meyer Assessment

排除标准

  • neurological conditions in addition to stroke that may affect motor function
  • other medical conditions likely to interfere with the ability to safely complete the study protocol
  • impaired cognitive functioning that influences the ability to give informed consent
  • severe neuropsychological disorders
  • visual impairment
  • severe upper-limb pain defined as > 7 on the Visual Analogue Scale

结局指标

主要结局

Changes in upper limb impairment

时间窗: Score changes before (T0) and after (T1) the 4 weeks of treatment and at 6-month follow-up (T2)

Motor recovery will be assessed through the Fugl Meyer Assessment - Upper Extremity

次要结局

  • Change in Spasticity(Score changes before (T0) and after (T1) the 4 weeks of treatment and at 6-month follow-up (T2))
  • Change in Activities of Daily Living(Score changes before (T0) and after (T1) the 4 weeks of treatment and at 6-month follow-up (T2))
  • Change in perceived quality of life(Score changes before (T0) and after (T1) the 4 weeks of treatment and at 6-month follow-up (T2))
  • Kinematic data(Parameters changes (e.g. hand peak velocities) before (T0) and after (T1) the 4 weeks of treatment)
  • Electroencephalogram(Data changes before (T0) and after (T1) the 4 weeks of treatment (4 weeks) and at 6-month follow-up (T2))
  • Treatment satisfaction(After 4 weeks)
  • Embodiment(After 4 weeks)
  • Cybersickness(After 4 weeks)

研究者

发起方
University Hospital of Ferrara
申办方类型
Other
责任方
Sponsor

研究点 (2)

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