跳至主要内容
临床试验/NCT05135533
NCT05135533已完成不适用

Cranial-nerve Non-invasive Neuromodulation and Dynamic Balance in Chronic Stroke Survivors

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 53 人开始时间: 2023年8月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
53
试验地点
1
主要终点
Change in Gait Speed

研究概览

简要总结

Portable Neuromodulation Stimulator (PoNS) is non-invasive stimulation device placed on the tongue to stimulate those brain regions understood to be important for maintaining balance. This research study aims to collect evidence that PoNS therapy along with balance training improves postural and walking stability post-stroke.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
22 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •At least six months since the onset of Ischemic or hemorrhagic stroke.
  • •Demonstrate residual paresis in the lower extremity (Fugl-Mayer lower extremity score < 34).
  • •Are able to provide informed consent demonstrated by their ability to weigh the consequences of participating versus not participating in the study.
  • •Can walk at least 10 feet with and without assistive device.
  • •Functional Gait Assessment score <22.

排除标准

  • •Pre-existing neurological disorders.
  • •Previous stroke affecting the other hemisphere .
  • •Severe arthritis or orthopedic problems that limit passive range of motion.
  • •Areas of recent bleeding or open wounds.
  • •Lack normal sensation on the tongue.
  • •Received treatment for cancer within the past year.
  • •Non-removable metal orthodontic devices.
  • •Oral health problems.
  • •Are sensitive to nickel, gold or copper.
  • •Chronic infectious diseases.
  • •Are pregnant.
  • •Have dementia

研究组 & 干预措施

Sham

Sham Comparator

干预措施: Sham (Device)

Portable Neuromodulation Stimulator

Experimental

干预措施: Portable Neuromodulation Stimulation (Device)

Portable Neuromodulation Stimulator

Experimental

干预措施: Gait and balance training (Other)

Sham

Sham Comparator

干预措施: Gait and balance training (Other)

结局指标

主要结局

Change in Gait Speed

时间窗: Pre-treatment, midpoint at four weeks, and post-treatment at 12 weeks

Self-selected comfortable walking overground walking speed in cm/s.

Change in Balance

时间窗: Pre-treatment, midpoint at four weeks, and post-treatment at at 12 weeks

Functional Gait Assessment (FGA) assesses stability during walking. The score ranges between 0 and 30 with lower scores indicative of poor dynamic balance.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Steven Kautz

Depertment Chair

Medical University of South Carolina

研究点 (1)

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