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Transcutaneous Superior Laryngeal Nerve Stimulation to Upregulate Swallowing Frequency and Urge to Swallow in Patients Living With ALS

2026年5月18日 更新者:Nova Southeastern University

Prospective, single-arm pilot study evaluating transcutaneous electrical nerve stimulation of the superior laryngeal nerve (TENS-SLN) in individuals with ALS.

Up to 5 participants with confirmed ALS and bulbar involvement will be enrolled.

Primary outcomes: swallowing frequency and perceived urge to swallow. Participants complete a baseline visit, followed by two supervised treatment sessions within one week, and a final post-treatment evaluation.

Optional visits (up to 2) may be used to individualize stimulation parameters prior to treatment.

Swallowing function will be assessed using physiological monitoring, fiberoptic endoscopy, and videofluoroscopic swallow study (VFSS).

TENS-SLN is a non-invasive neuromodulation approach targeting sensory pathways to facilitate swallowing without inducing muscle contraction.

This pilot study is designed to assess feasibility, safety, and preliminary effect sizes to inform future randomized trials, and is not powered to determine efficacy.

研究概览

详细说明

This prospective, single-arm interventional pilot study will evaluate the acute effects of transcutaneous electrical nerve stimulation of the superior laryngeal nerve (TENS-SLN) on swallowing function in individuals with amyotrophic lateral sclerosis (ALS). Up to five participants with confirmed ALS and bulbar involvement will be enrolled. The primary outcomes are swallowing frequency and perceived urge to swallow.

Participants will complete a baseline assessment followed by two supervised TENS-SLN treatment sessions conducted within a one-week period. Up to two additional visits may be performed prior to treatment to optimize individualized stimulation parameters. Treatment sessions may take place in the clinic or the participant's home under clinician supervision. A final in-clinic evaluation will be completed at the end of the study period. Swallowing function will be assessed using physiological monitoring, fiberoptic endoscopy, and videofluoroscopic swallow study (VFSS) at baseline and post-intervention.

TENS-SLN is a non-invasive neuromodulation approach that delivers low-intensity electrical stimulation via surface electrodes placed over the anatomically accessible superior laryngeal nerve in the anterior neck. The intervention is designed to enhance sensory input to swallowing-related neural circuits and facilitate swallow initiation without directly eliciting muscle contraction.

This pilot study is not powered to determine efficacy but is intended to assess feasibility, safety, and preliminary effect sizes to inform the design of future randomized controlled trials. All study procedures are performed for research purposes and are not part of standard clinical care.

研究类型

介入性

注册 (估计的)

5

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Racquel Garcia, SLPD, CCC-SLP
  • 电话号码:(954) 262-1271
  • 邮箱:rw602@nova.edu

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Confirmed diagnosis of ALS (El-Escorial Criteria)
  • ALS FRS Bulbar Subscore of ≤ 10 and ≥ 3.
  • Functional Oral Intake scale score ≥ 2

Exclusion Criteria:

  • A diagnosis of significant cognitive impairment or frontotemporal dementia per the treating neurologist or neuropsychologist,
  • Current nasogastric tube placement
  • Current head and neck carcinoma
  • Pacemaker or implanted defibrillator or history of diagnosed arrhythmia, bradycardia, or repeated attacks of hypotension,
  • Implanted vagal nerve stimulator
  • Current pregnancy
  • History of epilepsy
  • Infected, broken or inflamed skin on the neck, or impaired sensation at the site of sEMG or TENS placement
  • Living greater than 50 miles from the NSU clinic round trip
  • Any clinical reason that this stimulation may not be a suitable treatment according to the principal investigator.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:干预组
Transcutaneous Superior Laryngeal Nerve Stimulation to Upregulate Swallowing Frequency and Urge to Swallow in ALS

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Swallowing Frequency
大体时间:From enrollment to the end of the 7-day follow-up period
The count of swallows per unit time with predefined epochs
From enrollment to the end of the 7-day follow-up period
Urge-to-swallow
大体时间:Measured from enrollment to the end of the 7 day follow up period
patient reported urge to swallow during rest and stimulation periods on a modified Borg scale, 0 (very easy) to 10 (very difficult to elicit a swallow)
Measured from enrollment to the end of the 7 day follow up period

次要结果测量

结果测量
措施说明
大体时间
Body weight gain/loss
大体时间:At Day 1 and at Day 7
The total body weight (lbs)
At Day 1 and at Day 7
Maximum Expiratory Pressure
大体时间:From enrollment to the end of the 7-day follow up period
Maximum expiratory pressure achieved during forceful exhalation
From enrollment to the end of the 7-day follow up period
Lingual pressure assessment
大体时间:At baseline (Day 1) pre-procedural, on Day 1 post-procedure, and on Day 7
Maximum lingual pressure and saliva swallowing pressures will be obtained using the IOPI oral performance in 3 instances.
At baseline (Day 1) pre-procedural, on Day 1 post-procedure, and on Day 7
Peak cough flow
大体时间:One at enrollment and one at the end of the 7- day folow-up period
Maximum expiratory flow achieved during the expulsive phase of the cough (PCF, L/min)
One at enrollment and one at the end of the 7- day folow-up period
Videofluoroscopic Swallowing Evaluation
大体时间:At baseline and at the end of the 7-day follow-up period
Yale residue Scale to assess post-swallow residue in the pharynx following swallow trials. (5 point ordinal scale; graded 1 being none -5 being severe) Dynamic Imaging Grade of Swallowing Toxicity for FEES safety, efficiency, and total scores. (each subscore is graded on scale from 0-4; 0 being no impairment, being profound/life-threatening impairment)
At baseline and at the end of the 7-day follow-up period
Fiberoptic Endoscopic Evaluation of Swallowing (FEES)
大体时间:At baseline and again at the end of the 7 day follow up period
New Zealand Secretion Scale to assess oropharyngeal secretions and clearance response on a 7-point ordinal scale. (Maximum 7- Minimum 0) Laryngeal Kinematics: presence of vocal fold adduction and abduction
At baseline and again at the end of the 7 day follow up period
Body Weight (BMI)
大体时间:Day 1 - Day 7
Total BMI measured at Baseline (day 1) and at the end of th study (Day 7)
Day 1 - Day 7

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Lauren Tabor Gray, Ph.D CCC-SLP、Nova Southeastern University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月1日

初级完成 (估计的)

2026年12月1日

研究完成 (估计的)

2026年12月1日

研究注册日期

首次提交

2026年4月21日

首先提交符合 QC 标准的

2026年5月18日

首次发布 (实际的)

2026年5月26日

研究记录更新

最后更新发布 (实际的)

2026年5月26日

上次提交的符合 QC 标准的更新

2026年5月18日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

Data will be shared with the NSU study team and study collaborators. This includes Dr. Teresa Lever and Mario Awadala (University of Missouri). A clinical trial agreement is established to share this data, and verbiage is included in the informed consent document to inform participants of this agreement.

IPD 共享支持信息类型

  • 研究方案

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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