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临床试验/NCT07563387
NCT07563387Enrolling By Invitation不适用

Non-invasive Vagus Nerve Stimulation for Language Recovery in Aphasia

University of Florida1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2026年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
12
试验地点
1
主要终点
Adverse events

研究概览

简要总结

The goal of this research study is to evaluate a novel approach to improving speech recovery in those with acquired apraxia of speech. We will enroll participants with apraxia of speech resulting from stroke or brain injury to complete several tasks and intervention. Testing will take place four times over the course of the study and intervention will take place 5 days a week for 16 weeks. Overall, you can expect to spend up to 17 weeks participating in this study.

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults between 18-80
  • Native speakers of English or simultaneous bilinguals
  • At least 6 months post stroke or TBI
  • Diagnosed production type aphasia or apraxia of speech

排除标准

  • Additional cognitive or neurological impairments (Autism, schizophrenia, seizures, etc)
  • Language comprehension deficits
  • Medications that influence key neurotransmitters

研究组 & 干预措施

Treatment A

Experimental

non-invasive vagus nerve stimulation is administered alongside standard intervention

干预措施: taVNS (Device)

Treatment B

Placebo Comparator

sham stimulation is administered alongside standard intervention

干预措施: sham taVNS (Device)

结局指标

主要结局

Adverse events

时间窗: 6 months

Frequency and severity of adverse events will be monitored and evaluated for severity and impact on attrition.

Compliance

时间窗: 6 months

Percentage of the population that remains engaged in the study and completes all stimulation sessions.

次要结局

  • Change in speech production scores(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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