Tolerability and feasibility of at-home remotely supervised transcranial direct current stimulation (RS-tDCS): Single-center evidence from 6,779 sessions

被引:57
作者
Pilloni, Giuseppina [1 ]
Vogel-Eyny, Amy [1 ]
Lustberg, Matthew [1 ]
Best, Pamela [1 ]
Malik, Martin [2 ]
Walton-Masters, Lillian [3 ]
George, Allan [1 ]
Mirza, Ibraheem [1 ]
Zhovtis, Lana [1 ]
Datta, Abhishek [4 ,5 ]
Bikson, Marom [5 ]
Krupp, Lauren [1 ]
Charvet, Leigh [1 ,6 ]
机构
[1] NYU Grossman Sch Med, Dept Neurol, New York, NY USA
[2] Hackensack Meridian Sch Med, Nutley, NJ USA
[3] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Woodbury, PA USA
[4] Soterix Med Inc, Res & Dev, Woodbridge, NJ USA
[5] CUNY City Coll, Dept Biomed Engn, New York, NY USA
[6] 222 East 41st St,10th Floor, New York, NY 10017 USA
基金
美国国家卫生研究院;
关键词
Transcranial direct current stimulation; tDCS; At-home; Remote; Feasibility; Tolerability; SAFETY; COGNITION; CORTEX; GUIDE;
D O I
10.1016/j.brs.2022.04.014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The ability to deploy transcranial direct current stimulation (tDCS) at home is a key usability advantage to support scaling for pivotal clinical trials. We have established a home-based tDCS protocol for use in clinical trials termed remotely supervised (RS)-tDCS. Objective: To report the tolerability and feasibility of tDCS sessions completed to date using RS-tDCS in clinical trials. Methods: We analyzed tolerability (i.e., adverse events, AEs) reported in six Class I/II/III trials using RStDCS to study symptom outcomes over 10 to 60 daily applications. Across the six clinical trials, 308 participants (18-78 years old) completed an average of 23 sessions for a total of 6779 RS-tDCS administrations. The majority of participants were diagnosed with multiple sclerosis, and open-label trials included those diagnosed with a range of other conditions (e.g., Parkinson's disease, post-stroke aphasia, traumatic brain injury, cerebellar ataxia), with minimum-to-severe neurologic disability. Clinical trial feasibility (i.e., treatment fidelity and blinding integrity) was examined using two Class I randomized controlled trials (RCTs). Results: No serious AEs occurred. Across administrations, three sessions (0.04%) were aborted due to discomfort, but no participant discontinued due to tolerability. The AEs most commonly reported by participants were tingling (68%), itching (41%) and warmth sensation (42%) at the electrode site, and these were equally reported in active and sham tDCS conditions. The two Class I RCTs resulted in rapid enrollment, high fidelity to treatment completion, and blinding integrity. Conclusions: At-home RS-tDCS is tolerable, including when used over extended periods of time. Homebased RS-tDCS is feasible and can enable Class I tDCS clinical trial designs. (c) 2022 Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:707 / 716
页数:10
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