跳至主要内容
临床试验/DRKS00033115
DRKS00033115已完成Unknown

Rehabilitation based on hybrid neuroprosthesis: Evaluation of the feasibility, functionality, and usability of the system in post-stroke patient population - ReHyb

Schön Klinik Bad Aibling SE & Co. KG0 个研究点目标入组 24 人开始时间: 2023年12月1日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
N/a: Single Arm Study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • diagnosis of stroke (hemorrhagic or ischemic)
  • - hemiparesis of the upper limb (0 = MRC = 4)
  • - subacute (up to six months after acute event) or chronic (more than 6 months from the acute event) condition
  • - able to sit upright for the duration of the test ( ~1h)
  • - level of cognitive capacity to follow instructions related to the performance exercise

排除标准

  • - high level of spasticity (MAS: in general > 3, but > 2 for motorized joints)
  • - pain in the affected upper limb (NRS > 4)
  • - severe psychiatric disorder
  • - permanent neurologic symptoms present immediately before stroke
  • - physical conditions that can alter normal biomechanics (e.g. recent sprains or injuries, etc.)
  • - pregnant or nursing women
  • - no written informed consent from the patient or the legal representative
  • - active implantable devices (e.g., pacemaker)
  • - unstable medical condition
  • FES-related:
  • - metal implants within the stimulated area
  • - severe epilepsy or frequent epileptic seizures in the past
  • - wounds in the application area of the electrodes or measuring equipment
  • - no movement resulting from stimulation
  • Robot-related:
  • - inadequate fitting of the exoskeleton

研究者

相似试验