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Remotely Supervised Transcranial Direct Current Stimulation: An Update on Safety and Tolerability
Published on: October 7, 2017
Safety and tolerability of temporal interference stimulation in humans: A systematic review and meta-analysis of an
Ilya Demchenko1, Qiaowei Lin2, Yesha Patel2
1AI for Mental Health Program, St. Michael's Hospital, Unity Health Toronto, Toronto, ON, M5B 1M4, Canada; Institute of Medical Science, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, M5S 3H2, Canada; CRANIA NeuroModulation Institute (CNMI), University of Toronto, Toronto, ON, Canada.
Background:
Temporal interference stimulation (TIS) uses kilohertz-frequency currents to generate a low-frequency amplitude-modulated envelope within brain tissue, enabling deeper targeting while minimizing superficial stimulation. As human applications expand, a systematic evaluation of safety and tolerability is needed.
Methods:
Following PRISMA guidelines (PROSPERO: CRD420251081135), we searched Ovid MEDLINE, Embase, and APA PsycINFO (May 2, 2025) for peer-reviewed human TIS studies reporting safety or tolerability outcomes. Methodological quality and risk of bias were assessed using design-appropriate RoB 2, ROBINS-I, and Joanna Briggs Institute tools. Random-effects meta-analyses were conducted in R. Parallel-arm randomized controlled trials (RCTs) were synthesized using risk ratios (RRs), with sensitivity analyses using risk differences (RDs), alternative continuity corrections, and pooling models. Within-subject studies were summarized descriptively using pooled adverse event (AE) proportions, with additional sensitivity analyses by transformation, study quality, and AE-elicitation method.
Results:
Twenty-four studies (N = 853 participants; 21 RCTs, 3 non-randomized) were included. No serious AEs (SAEs) were reported. In parallel-arm RCTs (k = 5 arms; N = 192 participants), most AEs showed effects near null. Tingling was more frequent with active TIS (RR = 2.95; 95% CI, 1.25-7.00; RD = 0.18; 95% CI, 0.01-0.34). In within-subject studies (k = 20 arms; N = 531 participants), descriptive pooled AE proportions varied across outcomes, with the highest estimates observed for fatigue, sleepiness, and tingling.
Discussion:
TIS was generally well tolerated in humans, with predominantly mild, transient AEs and no SAEs reported. Evidence is limited to conservative parameters (~2 kHz; ≤2 mA/channel), small sample sizes, and short-term TIS applications.