基于家庭的经颅直流电刺激(tDCS)和运动想象治疗幻肢痛,利用统计学习预测治疗反应:开放标签研究方案。

Kevin Pacheco-Barrios, Alejandra Cardenas-Rojas, Paulo S de Melo, Anna Marduy, Paola Gonzalez-Mego, Luis Castelo-Branco, Augusto J Mendes, Karen Vásquez-Ávila, Paulo E P Teixeira, Anna Carolyna Lepesteur Gianlorenco, Felipe Fregni
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引用次数: 0

摘要

背景:幻肢痛(PLP)的治疗因其反应异质性和缺乏治疗途径而一直是一项挑战。本研究将评估基于远程家庭的 M1 阳极 tDCS 与运动想象相结合治疗幻肢患者的可行性,并评估该疗法的初步疗效、安全性和反应预测因素:这是一项试点、单臂、开放标签试验,我们将招募 10 名幻肢痛患者。研究将包括 20 个疗程。所有受试者都将接受主动阳极 M1 tDCS 与幻肢运动想象训练相结合的治疗。我们的主要研究结果将是这种联合干预的可接受性和可行性。此外,我们还将评估治疗后的初步临床(疼痛强度)和生理(运动抑制任务和心率变异性)变化。最后,我们将实施一个有监督的统计学习(SL)模型,以确定 PLP 患者治疗反应(对 tDCS 和幻肢运动想象)的预测因素。我们还将使用之前临床试验中的数据(总观察数据=224 [n=112 x 时间点=2)),用于我们的统计学习算法。这项开放标签研究的新前瞻性数据将作为独立的测试数据集:本方案建议评估一种新型神经调节联合干预措施的可行性,以便设计更大规模的远程临床试验,从而增加PLP患者获得安全有效治疗的机会。此外,这项研究还将使我们能够确定疼痛反应的可能预测因素和PLP临床内型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Home-based transcranial direct current stimulation (tDCS) and motor imagery for phantom limb pain using statistical learning to predict treatment response: an open-label study protocol.

Background: Phantom limb pain (PLP) management has been a challenge due to its response heterogeneity and lack of treatment access. This study will evaluate the feasibility of a remotely home-based M1 anodal tDCS combined with motor imagery in phantom limb patients and assess the preliminary efficacy, safety, and predictors of response of this therapy.

Methods: This is a pilot, single-arm, open-label trial in which we will recruit 10 subjects with phantom limb pain. The study will include 20 sessions. All participants will receive active anodal M1 tDCS combined with phantom limb motor imagery training. Our primary outcome will be the acceptability and feasibility of this combined intervention. Moreover, we will assess preliminary clinical (pain intensity) and physiological (motor inhibition tasks and heart rate variability) changes after treatment. Finally, we will implement a supervised statistical learning (SL) model to identify predictors of treatment response (to tDCS and phantom limb motor imagery) in PLP patients. We will also use data from our previous clinical trial (total observations=224 [n=112 x timepoints = 2)) for our statistical learning algorithms. The new prospective data from this open-label study will be used as an independent test dataset.

Discussion: This protocol proposes to assess the feasibility of a novel, neuromodulatory combined intervention that will allow the design of larger remote clinical trials, thus increasing access to safe and effective treatments for PLP patients. Moreover, this study will allow us to identify possible predictors of pain response and PLP clinical endotypes.

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