针对慢性神经性疼痛的视听刺激疗法:一项模拟对照随机临床试验

Laura Tabacof, Rebecca Howard, Jeffrey Bower, Erica Breyman, Sophie Dewil, Jenna Tosto-Mancuso, Richard Hanbury, Brandon Carmouche, Mark Robberson, Adam Fry, David Putrino
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引用次数: 0

摘要

神经性疼痛(NP)影响着 10% 的普通人群,降低了数百万美国人的生活质量,并导致更高的身体和精神保健费用。目前最广泛使用的治疗神经性疼痛的方法是药物治疗,但疗效有限且副作用大。这项随机对照试验探讨了可穿戴视听刺激神经调控设备(Sana)作为一种新型干预措施对 64 名慢性 NP 患者的疗效。结果分别在基线、每天使用指定的 Sana 或 Sham 设备 8 周后以及停止使用 4 周后进行评估。对于主要结果(神经病理性疼痛症状量表总计),在第 14 周时,主动治疗组的改善幅度大于被动治疗组(平均差异 = 10.04,p = 0.01),具有统计学意义。两组患者在治疗期结束时(第 10 周)均有明显改善,主动治疗组在停用 4 周后仍能保持这种改善,而被动治疗组则几乎恢复到基线水平(主动治疗组变化 = 13.26,p = 0.001 | 被动治疗组变化 = 3.22,p = 0.214)。与模拟治疗组相比,主动治疗组的参与者使用抗焦虑药、鸦片制剂、抗抑郁药和抗惊厥药的情况明显减少。这项研究提供了有力的证据,支持新型 AVS 设备在持久改善 NP 方面的疗效,在 14 周时优于 Sham。Sana 设备还可以减少患者对止痛药物的依赖,是一种安全易用的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Audio-Visual Stimulation Therapy for Chronic Neuropathic Pain: A Sham-Controlled Randomized Clinical Trial
Neuropathic Pain (NP) affects 10% of the general population, decreasing quality of life for millions of Americans and contributing to higher physical and mental health care costs. The most widely used treatments for NP involve medications that show limitations in efficacy and burdensome side effects. This randomized controlled trial explored the efficacy of a wearable Audio-Visual Stimulation neuromodulation device (Sana) as a novel intervention for chronic NP in 64 participants. Outcomes were assessed at baseline, after 8-weeks of daily use of the assigned Sana or Sham device, and after 4 weeks of discontinued use. For the main outcome (Neuropathic Pain Symptom Inventory total), there were statistically significant improvements in the Active arm that were greater than those in the Sham Arm at Week-14 (Mean Difference = 10.04, p = 0.01). Both groups showed significant improvements at the end of the treatment period (Week-10), and the Active arm maintained this improvement after an additional 4 weeks of non-use, while the Sham arm almost returned to baseline (Active Change = 13.26, p <=0.001 | Sham Change = 3.22, p = 0.214). Participants in the Active arm had significant decreases in use of anxiolytic, opiate, antidepressant, and anticonvulsant medications compared to the Sham arm. The study provides strong evidence supporting the efficacy of a novel AVS Device in generating durable improvements in NP, with superiority over Sham at 14 weeks. The Sana device may also reduce the reliance on pain medications and is a safe and easy to use treatment option for patients.
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