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
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