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临床试验/NL-OMON49919
NL-OMON49919招募中不适用

Early and intensive motor training to enhance neurological recovery and function in people with spinal cord injury - SCI-MT

niversity of Sydney, Australia0 个研究点目标入组 16 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
16

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
16 至 64(—)

入选标准

  • People will be eligible to participate if they:
  • 1. have sustained a traumatic or non-traumatic SCI below C4 (neurological
  • level) in the preceding 8 weeks.
  • 2. have an AIS A lesion with motor function more than three levels below the
  • motor level (on one or both sides), or an AIS C or AIS D lesion (as defined by
  • the International Standards for the Neurological Classification of SCI).
  • 3. are male or female, over the age of 16 years at the time of signing informed
  • 4. have been cleared by the medical team to commence rehabilitation (as
  • documented in the participant*s medical files).
  • 5. are likely to remain an inpatient for the next 10 weeks.
  • 6. understand and voluntarily sign an informed consent form prior to any study
  • related assessments/procedures being conducted.
  • 7. are willing and able to adhere to the study visit schedule and other
  • protocol requirements.

排除标准

  • People will be eligible to participate if they:
  • 1. have sustained a traumatic or non-traumatic SCI below C4 (neurological
  • level) in the preceding 8 weeks.
  • 2. have an AIS A lesion with motor function more than three levels below the
  • motor level (on one or both sides), or an AIS C or AIS D lesion (as defined by
  • the International Standards for the Neurological Classification of SCI).
  • 3. are male or female, over the age of 16 years at the time of signing informed
  • consent (additional consent from a parent or guardian will be attained for
  • those aged under 18 years).
  • 4. have been cleared by the medical team to commence rehabilitation (as
  • documented in the participant*s medical files).
  • 5. are likely to remain an inpatient for the next 10 weeks.
  • 6. understand and voluntarily sign an informed consent form prior to any study
  • related assessments/procedures being conducted.
  • 7. are willing and able to adhere to the study visit schedule and other
  • protocol requirements.

研究者

发起方
niversity of Sydney, Australia

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