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临床试验/NCT07719829
NCT07719829尚未招募不适用

Paired VNS For TBI Rehabilitation

Stony Brook University0 个研究点目标入组 20 人开始时间: 2027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
尚未招募
入组人数
20
主要终点
Number of Participants With Device- or Procedure-Related Adverse Events

研究概览

简要总结

This study is evaluating whether pairing vagus nerve stimulation (VNS) with structured upper limb rehabilitation therapy can improve arm and hand function in individuals with chronic moderate to severe traumatic brain injury (TBI) and subsequent motor deficits.

Many people who survive a TBI experience long-term weakness, poor coordination, and difficulty using one arm or hand. These motor impairments can significantly affect independence and quality of life. Traditional rehabilitation can help, but recovery is often incomplete.

Vagus nerve stimulation (VNS) is an FDA-approved therapy for certain neurological conditions and involves a small device implanted under the skin in the chest with a lead connected to the vagus nerve in the neck. The device delivers mild electrical pulses to the nerve. In this study, VNS will be paired with goal-directed upper limb rehabilitation exercises. The stimulation is delivered during specific movements in therapy sessions. This "paired stimulation" approach is designed to enhance neuroplasticity - the brain's ability to reorganize and form new connections - which may improve motor recovery.

The VNS device used in this study is FDA-approved for other conditions. However, its use paired with rehabilitation for upper limb recovery after traumatic brain injury is investigational.

Participants in this study will:

Undergo surgical implantation of the VNS device.

Participate in structured upper limb rehabilitation therapy sessions where stimulation is paired with specific movements.

Complete follow-up visits and assessments to measure changes in arm and hand function, strength, dexterity, and overall recovery.

The main goal of the study is to determine whether paired VNS and rehabilitation improves upper limb motor function compared to rehabilitation alone. Safety will also be closely monitored, including surgical outcomes and any device-related effects.

This study may help determine whether VNS paired with rehabilitation is a safe and effective way to enhance motor recovery after traumatic brain injury. Findings from this research could contribute to improved treatment strategies for individuals living with long-term motor impairments following TBI. If the results are promising, future studies plan to also include patients with acute TBI.

Participation is voluntary. All participants will be carefully evaluated to determine eligibility, and informed consent will be obtained before enrollment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Age 22-80 years
  • History of severe TBI (initial GCS ≤ 8)
  • Regained consciousness with capacity to consent to the study
  • At least six months since injury
  • Full recovery of consciousness with command following (mGCS = 6)
  • Ongoing motor impairment with dependence in activities of daily living (modified Rankin Scale, mRS = 3-4)
  • Clinically stable for VNS implantation

排除标准

  • No capacity to consent to the study
  • History of stroke
  • History of cognitive disorder or other neurodegenerative disorder
  • History of epilepsy treated by VNS
  • History of brain tumors (primary or metastatic)
  • Requires diathermy
  • Previously implanted vagus nerve stimulator
  • Extensive prior neck surgery preventing dissection of the vagus nerve
  • History of severe spasticity, vagus nerve damage, or hearing loss

研究组 & 干预措施

VNS Group

Experimental

Group to be implanted with VNS devices

干预措施: VNS for TBI group (Device)

结局指标

主要结局

Number of Participants With Device- or Procedure-Related Adverse Events

时间窗: 6 Weeks

Adverse events related to VNS device implantation or stimulation will be recorded and graded using CTCAE v5.0.

Change in Upper Limb Range of Motion as Assessed by SeeMe Movement Analysis

时间窗: 6 Weeks

Video-based kinematic analysis of upper limb range of motion, comparing baseline (pre-surgery) to post-training (6 weeks after VNS-paired rehabilitation).

次要结局

  • Change in Disability Rating Scale (DRS) Score(1 Year)
  • Change in Coma Recovery Scale-Revised (CRS-R) Score(6 Weeks)
  • Change in Wolf Motor Function Test (WMFT) Performance Time(6 Weeks)
  • Change in Fugl-Meyer Assessment Upper Extremity (FMA-UE) Score(6 Weeks)
  • Change in Motor Activity Log (MAL) Score(1 Year)
  • Change in EQ-5D-5L Index Score(1 Year)

研究者

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

Sima Mofakham

Associate Professor of Neurosurgery

Stony Brook University

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