Frontiers in Neurology (Jul 2024)

Brain-computer interface on wrist training with or without neurofeedback in subacute stroke: a study protocol for a double-blinded, randomized control pilot trial

  • Myeong Sun Kim,
  • Myeong Sun Kim,
  • Hyunju Park,
  • Hyunju Park,
  • Ilho Kwon,
  • Ilho Kwon,
  • Kwang-Ok An,
  • Joon-Ho Shin,
  • Joon-Ho Shin

DOI
https://doi.org/10.3389/fneur.2024.1376782
Journal volume & issue
Vol. 15

Abstract

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BackgroundAfter a stroke, damage to the part of the brain that controls movement results in the loss of motor function. Brain-computer interface (BCI)-based stroke rehabilitation involves patients imagining movement without physically moving while the system measures the perceptual-motor rhythm in the motor cortex. Visual feedback through virtual reality and functional electrical stimulation is provided simultaneously. The superiority of real BCI over sham BCI in the subacute phase of stroke remains unclear. Therefore, we aim to compare the effects of real and sham BCI on motor function and brain activity among patients with subacute stroke with weak wrist extensor strength.MethodsThis is a double-blinded randomized controlled trial. Patients with stroke will be categorized into real BCI and sham BCI groups. The BCI task involves wrist extension for 60 min/day, 5 times/week for 4 weeks. Twenty sessions will be conducted. The evaluation will be conducted four times, as follows: before the intervention, 2 weeks after the start of the intervention, immediately after the intervention, and 4 weeks after the intervention. The assessments include a clinical evaluation, electroencephalography, and electromyography using motor-evoked potentials.DiscussionPatients will be categorized into two groups, as follows: those who will be receiving neurofeedback and those who will not receive this feedback during the BCI rehabilitation training. We will examine the importance of motor imaging feedback, and the effect of patients’ continuous participation in the training rather than their being passive.Clinical Trial Registration: KCT0008589.

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