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Anodal tDCS of left motor cortex reduces experimental thermal pain in healthy adults

Anodal tDCS of left motor cortex reduces experimental thermal pain in healthy adults
Photo by Navy Medicine / Unsplash
Key Takeaway
Interpret experimental tDCS pain modulation findings cautiously for clinical pain.

A triple-blind, pre-registered, randomized within-subject crossover trial investigated the effects of transcranial direct current stimulation (tDCS) on experimentally evoked thermal pain in 50 healthy adults. Participants received anodal, cathodal, and sham stimulation of the left motor cortex (M1) in a crossover design, with pain testing occurring over a 35-minute post-stimulation period. Blinding assessments confirmed participants were unable to reliably identify the sham session.

Compared to cathodal M1-tDCS, anodal stimulation significantly reduced pain with a large effect size (Cohen's d = 0.93, P < 0.001). Anodal tDCS also significantly reduced pain compared to sham stimulation (Cohen's d = 0.85, P < 0.001). Conversely, cathodal tDCS increased pain relative to sham (Cohen's d = 0.34, P < 0.01). A secondary finding showed anodal tDCS modestly increased reaction time in the ipsilateral hand (Cohen's d = 0.16, P < 0.05), but this effect was uncorrelated with the analgesic response (P > 0.10).

Safety and tolerability data were not reported. Key limitations, including potential carryover effects in the crossover design, were also not reported. The study's triple-blind, pre-registered design and within-subject comparisons strengthen internal validity. However, the direct clinical relevance is restrained as the findings are derived from an experimental pain model in healthy volunteers, not from patients with clinical pain conditions.

Study Details

Study typeRct
Sample sizen = 50
EvidenceLevel 2
PublishedApr 2026
View Original Abstract ↓
Transcranial direct current stimulation (tDCS) is a noninvasive brain stimulation technique with growing potential for pain modulation. However, previous studies have often been limited by small sample sizes, limited outcome reliability, and blinding issues. Pre-registered randomized trials are needed to establish efficacy and reproducibility. Here, we report results from a pre-registered, triple-blind, randomized within-subject crossover trial (N = 50), investigating the effects of left motor cortex (M1) tDCS on experimentally evoked thermal pain in healthy adults. Participants underwent individualized pain calibration, then received anodal, cathodal, and sham M1-tDCS in counterbalanced order on separate visits 4 or more days apart. We assessed post-tDCS thermal pain, potential blinding, side effects, and reaction time during pain rating. Anodal tDCS significantly reduced pain compared with cathodal and sham stimulation ( P < 0.001, Cohen's d = 0.93 and 0.85, respectively; P < 0.001). Cathodal tDCS increased pain relative to sham (Cohen's d = 0.34, P < 0.01). These effects remained stable throughout the 35-minute post-tDCS pain testing period, with no evidence of decay over time. Blinding assessments confirmed that participants were unable to reliably identify the sham session. Anodal tDCS also modestly increased reaction time in the left (ipsilateral) hand ( P < 0.05, Cohen's d = 0.16), consistent with interhemispheric inhibition, which was uncorrelated with analgesia ( P > 0.10). This study provides strong evidence for reliable and polarity-dependent modulation of experimental pain by M1-tDCS.
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