4.6 Article

Motor Activated Auricular Vagus Nerve Stimulation as a Potential Neuromodulation Approach for Post-Stroke Motor Rehabilitation: A Pilot Study

Journal

NEUROREHABILITATION AND NEURAL REPAIR
Volume 37, Issue 6, Pages 374-383

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/15459683231173357

Keywords

transcutaneous auricular vagus nerve stimulation; taVNS; motor rehabilitation; stroke; motor activated auricular vagus nerve stimulation; MAAVNS; tVNS

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A study found that transcutaneous auricular vagus nerve stimulation (taVNS) combined with motor rehabilitation can improve post-stroke motor function. The motor activated auricular vagus nerve stimulation (MAAVNS) method, which synchronizes stimulation with movement, showed greater efficacy compared to unpaired taVNS.
Background Implanted vagus nerve stimulation (VNS), when synchronized with post-stroke motor rehabilitation improves conventional motor rehabilitation training. A non-invasive VNS method known as transcutaneous auricular vagus nerves stimulation (taVNS) has emerged, which may mimic the effects of implanted VNS. Objective To determine whether taVNS paired with motor rehabilitation improves post-stroke motor function, and whether synchronization with movement and amount of stimulation is critical to outcomes. Methods We developed a closed-loop taVNS system for motor rehabilitation called motor activated auricular vagus nerve stimulation (MAAVNS) and conducted a randomized, double-blind, pilot trial investigating the use of MAAVNS to improve upper limb function in 20 stroke survivors. Participants attended 12 rehabilitation sessions over 4-weeks, and were assigned to a group that received either MAAVNS or active unpaired taVNS concurrently with task-specific training. Motor assessments were conducted at baseline, and weekly during rehabilitation training. Stimulation pulses were counted for both groups. Results A total of 16 individuals completed the trial, and both MAAVNS (n = 9) and unpaired taVNS (n = 7) demonstrated improved Fugl-Meyer Assessment upper extremity scores (Mean +/- SEM, MAAVNS: 5.00 +/- 1.02, unpaired taVNS: 3.14 +/- 0.63). MAAVNS demonstrated greater effect size (Cohen's d = 0.63) compared to unpaired taVNS (Cohen's d = 0.30). Furthermore, MAAVNS participants received significantly fewer stimulation pulses (Mean +/- SEM, MAAVNS: 36 070 +/- 3205) than the fixed 45 000 pulses unpaired taVNS participants received (P < .05). Conclusion This trial suggests stimulation timing likely matters, and that pairing taVNS with movements may be superior to an unpaired approach. Additionally, MAAVNS effect size is comparable to that of the implanted VNS approach.

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