ACTRN12621000197831已完成未知
Electrical stimulation combined with strength training to increase the strength of very weak muscles in people with recent spinal cord injury. A randomised controlled trial
orthern Sydney Local Health District (Kolling Institute, Royal North Shore Hospital), John Walsh Centre for Rehabilitation Research0 个研究点目标入组 60 人开始时间: 2021年2月25日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 60
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
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •A person will be eligible to participate if they:
- •1.have a recent complete or incomplete SCI (as defined by the International Standards for Neurological classification of SCI) that was sustained less than six months prior
- •2.have partial paralysis in a major muscle group on one side of the body (i.e., elbow flexors or extensors, wrist flexors or extensors, knee flexors or extensors, ankle dorsiflexors or plantarflexors)
- •3.have less than grade 3 on the 13 point manual muscle scale (that is they are unable to move through full range against gravity)
- •4.are an inpatient of one of the participating SCI units and are likely to remain there for the duration of their involvement in the trial (i.e., approximately 9 weeks) or are being discharged home to the local area surrounding the hospital
- •5.are aged 18 years or over at the time of consent
- •6.are willing to participate in the trial
- •7.are free of any other type of neurological condition or injury
排除标准
- •A person is excluded from participation if they:
- •1.have any condition preventing testing or training of the target muscle
- •2.are not able to evoke a strong electrically stimulated contraction with the training parameters
- •3.have paralysis in the target muscle
- •4.are unable to co-operate (e.g. a serious medical condition, cognitive impairment, drug dependency, psychiatric illness, and behavioural problem)
- •5.do not speak the national language sufficiently well to provide informed consent
研究者
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