NL-OMON56022尚未招募不适用
Myokines and cognitive aging in people with spinal cord injury: a single case experimental design study - myokines and cognitive aging in SCI
Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 15 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
- 尚未招募
- 发起方
- 入组人数
- 15
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
- 18 至 99（—）
入选标准
- •-Persons with spinal cord injury
- •-Completeness of injury: AIS A, B or C
- •-Level of injury: L2 or higher
- •-At least 18 years old
- •-Chronic stage (> 1 year) since injury
- •-No previous surgery to the quadriceps muscles
- •-Able to use apps on smartphone (i.e. participants should have their own
- •smartphone and should not have disabilities that impair them to operate it
- •independently)
- •-Able to follow the instructions of placing the surface electrodes of the NMES
- •device correctly or to have someone else put the electrodes for them
- •-Dutch as a native language
排除标准
- •-Malignant processes, or history of undergoing chemotherapy, or history of
- •radiotherapy to the head
- •-No visible or palpable contraction of the quadriceps muscle upon electrical
- •stimulation
- •-Intolerance to electrical stimulation of the quadriceps muscle
- •-Recent or current participation in an electrical stimulation-induced exercise
- •or therapy program in which regular electrical stimulation was given (up to 6
- •months prior to study inclusion)
- •-Known neurodegenerative disorder, such as Alzheimer*s disease or Parkinson*s
- •-Known psychiatric disorder, such as major depressive disorder or bipolar
- •-Current pressure ulcer
- •-History of severe autonomic dysreflexia
- •-Metal implants in the electrical stimulation area
- •-Intrathecal baclofen (ITB) device
- •-Pregnancy
研究者
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