Reduction of Anxiety-Related Symptoms Using Low-Intensity Ultrasound Neuromodulation on the Auricular Branch of the Vagus Nerve: Preliminary Study.

JMIR neurotechnology Pub Date : 2025-05-01 eCollection Date: 2025-01-01 DOI:10.2196/69770
Izzy Kohler, Jon Hacker, Ethan Martin
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Abstract

Background: Neuromodulation of the auricular branch of the vagus nerve using low-intensity focused ultrasound (LIFU) is an emerging mode of treatment for anxiety that could provide a complementary or alternative treatment modality for individuals who are refractory to conventional interventions. The proposed benefits of this technology have been largely unexamined with clinical populations. Further research is required to understand its clinical potential and use in improving and managing moderate to severe symptoms.

Objectives: The aim of this study was to do a preliminary investigation into the efficacy, safety, and usability of the wearable headset that delivers LIFU to the auricular branch of the vagus nerve for the purpose of alleviating anxiety disorder symptoms.

Methods: This study was a pre-post intervention study design for which we recruited 28 participants with a Beck Anxiety Inventory score of 16 points or greater. Participants completed 5 minutes of treatment daily consisting of LIFU neuromodulation delivered to the auricular branch of the vagus nerve. Participants did this for a period of 4 weeks. Assessments of anxiety symptom severity (Beck Anxiety Inventory), depression symptom severity (Beck Depression Inventory), posttraumatic stress disorder symptom severity (Post Traumatic Stress Disorder Checklist for the Diagnostic and Statistical Manual of Mental Disorders [Fifth Edition]), and sleep quality (Pittsburgh Sleep Quality Index) were taken prior to starting treatment and weekly for 4 weeks of treatment. Usability and safety were also assessed using an exit questionnaire and adverse event logging.

Results: After completing 4 weeks of LIFU neuromodulation to the auricular branch of the vagus nerve, the average Beck Anxiety Inventory score decreased by 14.9 (SD 10.6) points (Cohen d=1.06; P<.001), the average Beck Depression Inventory score decreased by 10.3 (SD 7.8) points (Cohen d=0.81; P<.001), the average Post Traumatic Stress Disorder Checklist for the Diagnostic and Statistical Manual of Mental Disorders (Fifth Edition) score decreased by 20.0 (SD 20.5) points (Cohen d=0.94; P<.001), and the average Pittsburgh Sleep Quality Index score decreased by 2.2 (SD 3.1) points (Cohen d=0.65; P=.001). On the exit questionnaire, participants rated the treatment highly for ease of use, effectiveness, and worthiness of the time invested. Only 1 adverse event was reported throughout the entire trial, which was mild and temporary.

Conclusions: This preliminary study provided justification for further research into the efficacy, safety, and feasibility of using LIFU to modulate the auricular branch of the vagus nerve and reduce the symptoms of anxiety, depression, and posttraumatic stress disorder.

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低强度超声神经调节迷走神经耳支减轻焦虑相关症状的初步研究
背景:使用低强度聚焦超声(LIFU)对迷走神经耳支进行神经调节是一种新兴的焦虑治疗模式,可以为难以接受常规干预的个体提供补充或替代治疗方式。这项技术的益处在很大程度上没有经过临床人群的检验。需要进一步研究以了解其临床潜力以及在改善和管理中度至重度症状方面的用途。目的:本研究的目的是对可穿戴式耳机的有效性、安全性和可用性进行初步调查,该耳机将LIFU输送到迷走神经耳支,以减轻焦虑障碍症状。方法:本研究采用干预前后研究设计,我们招募了28名贝克焦虑量表得分为16分或更高的参与者。参与者每天完成5分钟的治疗,包括传递给迷走神经耳支的LIFU神经调节。参与者这样做了4周。治疗开始前和治疗4周后,每周进行焦虑症状严重程度(贝克焦虑量表)、抑郁症状严重程度(贝克抑郁量表)、创伤后应激障碍症状严重程度(精神障碍诊断与统计手册[第五版]创伤后应激障碍检查表)和睡眠质量(匹兹堡睡眠质量指数)评估。可用性和安全性也通过退出问卷和不良事件记录进行评估。结果:完成4周的LIFU神经调节迷走神经耳支后,Beck焦虑量表评分平均下降14.9分(SD 10.6)分(Cohen d=1.06; Pd=0.81;《精神障碍诊断与统计手册(第五版)》评分平均下降20.0分(SD 20.5)分(Cohen d=0.94; Pd=0.65; P= 0.001)。在退出问卷中,参与者对治疗的易用性、有效性和投入时间的价值给予了很高的评价。在整个试验过程中,仅报告了1例轻微和暂时的不良事件。结论:本初步研究为进一步研究LIFU调节迷走神经耳支,减轻焦虑、抑郁和创伤后应激障碍症状的有效性、安全性和可行性提供了依据。
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