Assessment of Feasibility and Statistical Reliability of Functional Outcomes Measurement in Neuromuscular Patients Without Trial Site Visiting by Standard Functional Scales and by Special Autonomic Device in Double-blind, Placebo Controlled Study of Cervical Spinal Cord Transdermal Direct Current Stimulation in Patients With Spinal Muscular Atrophy
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 发起方
- 试验地点
- 2
- 主要终点
- Strength Changes from baseline measured by handheld myometry after spinal cord direct current stimulation of different intensity
研究概览
简要总结
Clinical trials organization in several neuromuscular disorders (NMD) has some specific issues. Nonambulant status and difficulties with transportation are among them. Moreover a lot of patients with NMD have so poor condition that even short transportation is able to worse it. Such situation forces researchers to limit a region of recruitment for clinical trials and to exclude from trials more severe subgroup of patients, which cause additional issues especially for rare diseases.
The purpose of this study is to prove hypothesis about possibility to reliably monitor patient condition remotely, without trial site visiting. Visit-free study design is potentially able to widen eligible patient population and to decrease patient dropout rate as well as burden of numerous assessments. Meanwhile assessment frequency could be increased enabling monitoring of short fluctuations in patients' condition.
Spinal muscular atrophy (SMA) is a rare neuromuscular condition to which all mentioned above issues are completely applicable. Direct current stimulation (DCS) of neural structures is well studied and safe intervention, however, its effects on SMA patients' strength and durability has not been reported for today. The investigators suppose that investigation of DCS action in SMA patient population is an adequate model for visit-free design feasibility, reliability and sensitivity evaluation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 5 Years 至 —(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Signed informed consent
- •5q SMA confirmed by molecular testing
排除标准
- •Need for ventilation
- •Hypersensitivity (pain or allergic reaction) to current stimulation
研究组 & 干预措施
Zero-strength of direct current stimulation
Sham transdermal direct current stimulation of cervical spinal cord
干预措施: Direct current stimulation of cervical spinal cord (Other)
100 microamperes direct current stimulation
Transdermal direct current stimulation of cervical spinal cord
干预措施: Direct current stimulation of cervical spinal cord (Other)
1 milliampere direct current stimulation
Transdermal direct current stimulation of cervical spinal cord
干预措施: Direct current stimulation of cervical spinal cord (Other)
结局指标
主要结局
Strength Changes from baseline measured by handheld myometry after spinal cord direct current stimulation of different intensity
时间窗: Before and 0, 15, 30 minutes after spinal cord direct current stimulation
次要结局
- Short time fluctuations of Hammersmith Functional Motor Scale indexes(Three times, three days consecutive measurement, every two months, assessed up to 6 months)
