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临床试验/KCT0003762
KCT0003762已完成未知

A single-center, randomized, single blind, parallel design investigator study for finding validity items, evaluation criteria, and evaluation methods to evaluate the effect of gait rehabilitation using a rehabilitation robot(Healbot T) on walking ability for stroke patients who can walk independently or with supplementary help

Asan Medical Center0 个研究点目标入组 52 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
52

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 o Limit(—)
性别
All

入选标准

  • 1. Stroke patients over 19 years old
  • 2. Patients who are able to board the Healbot T and more than FAC (Functional Ambulation Category) 2
  • 3. Patients who were able to walk independently before the onset of stroke
  • 4. Patients who wrote the agreement

排除标准

  • 1. Patients who have serious difficulties in communication such as serious cognitive disorders or speech disorders.
  • 2. Patients with limited range of motion, such as the construction of joints (patients with musculoskeletal disorders, ex: pain due to arthritis)
  • 3. Patients who have ulcers that have bedsores, skin diseases, wounds or unhealed ulcers at the area touching cuff or harness.
  • 4. Patients with uncontrolled hypertension or orthostatic hypotension
  • 5. Patients who can not tolerate robot walking due to cardiovascular disease, heart failure, malignant disease, lung disease, nervous system disease, diabetes, etc.
  • 6. Patients with severe osteoporosis who are predicted to develop fractures
  • 7. Those who have difficulty walking because of severe deformity or pain in the legs
  • 8. Those who are suffering from severe mental illness, neuropathy or who are significantly less cooperative
  • 9. Pregnant women
  • 10. Patients with severe stiffness over Modified Ashworth Scale 3
  • 11. Patients withe tremor
  • 12. Those who weigh more than 100 kg
  • 13. Patients who heigh less than 150 cm or more than 185 cm
  • 14. Patients who participated in the rehabilitation robot study for stroke and were within 30 days of the end visit
  • 15. In addition, if the researcher judges that participation in this study is inappropriate

研究者

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