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Decoupling simultaneous motor imagination and execution via orthogonal ECoG neural representations
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  • Published: 31 March 2026

Decoupling simultaneous motor imagination and execution via orthogonal ECoG neural representations

  • Leonardo Pollina  ORCID: orcid.org/0009-0007-8648-40911,
  • Lucas Struber  ORCID: orcid.org/0000-0002-3890-91002,
  • Valeria de Seta  ORCID: orcid.org/0000-0001-8796-87751,3,
  • Eleonora Russo  ORCID: orcid.org/0000-0002-6215-63054,
  • Serpil Karakas2,
  • Stephan Chabardes2,5,
  • Tetiana Aksenova2,
  • Guillaume Charvet  ORCID: orcid.org/0000-0003-4938-94192,
  • Solaiman Shokur  ORCID: orcid.org/0000-0003-2251-71421,4,6 na1 &
  • …
  • Silvestro Micera  ORCID: orcid.org/0000-0003-4396-82171,4,6 na1 

Nature Communications , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biomedical engineering
  • Neural decoding

Abstract

The brain coordinates multiple parallel motor programs, ensuring synergy and preventing interference during movements. Yet, performance often degrades when brain–machine interfaces are used during concurrent tasks or ongoing movements. We suggest that latent neural representations may represent a strategy to solve this issue. In this study, we addressed this question using neural signals from a tetraplegic individual with partial residual motor function, implanted with a wireless epidural electrocorticography (ECoG) device. By adapting dimensionality reduction techniques, we found that motor execution and motor imagery span partially overlapping subspaces in mesoscale neural signals, shaped by specific frequency band contributions. Despite substantial shared variance, we show that identifying orthogonal, condition-specific dimensions enables successful decoding of executed and imagined movements, even when performed simultaneously. These findings show that ECoG signals can expose separable neural subspaces, allowing executed and imagined actions to be harnessed independently and in concert. This opens a promising avenue to develop brain–machine interfaces that can simultaneously control multiple external devices or operate alongside natural movements.

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Data availability

All data supporting the findings of this study are available within the article and its supplementary files. Any additional requests for information can be directed to and will be fulfilled by the corresponding author. Source data are provided with this paper. The neural data (only bandpass filtered in [1,250] Hz as well as fully preprocessed) have been deposited in the Zenodo public database: https://doi.org/10.5281/zenodo.18703800. Source data are provided with this paper.

Code availability

The code supporting the analyses presented in this study is available in the public Zenodo database: https://doi.org/10.5281/zenodo.18317718.

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Acknowledgements

The authors sincerely thank the participant for his invaluable time, dedication, and commitment throughout the data collection process. We also extend our gratitude to the multidisciplinary technical and clinical teams at Clinatec (CEA-LETI and CHU-Grenoble Alpes) for their involvement in the BCI &Tetraplegia clinical trial (NCT02550522), which enabled the advancements presented in this work. Finally, we thank Vincent Auboiroux for his assistance in providing medical reconstruction images of the implant location. S.M. and E.R. were supported by the #NEXTGENERATIONEU (NGEU) and funded by the Ministry of University and Research (MUR), National Recovery and Resilience Plan (NRRP), project: MNESYS (PE0000006)—A Multiscale integrated approach to the study of the nervous system in health and disease (DN. 1553 11.10.2022). S.M. also received support from two additional NRRP projects: THE (IECS00000017)—Tuscany Health Ecosystem (DN. 1553 11.10.2022), and BRIEF (IR0000036) –Biorobotics Research and Innovation Engineering Facilities (DN. 103 17.06.2022). L.P., V.d.S., S.M., and S.S. were supported by the Bertarelli Foundation and the Swiss National Science Foundation (Grant Number 10003473). L.S., S.K., S.C., T.A., and G.C. were supported by the CEA (Recurrent Funding), the Carnot Institute CEA-Leti, the French Ministry of Health and Research (PHRC 15-124), and the Fonds de dotation Clinatec (and its sponsors Malakoff Humanis, Covéa and Klésia).

Author information

Author notes
  1. These authors contributed equally: Solaiman Shokur, Silvestro Micera.

Authors and Affiliations

  1. Translational Neural Engineering Laboratory, Neuro-X Institute, EPFL, Geneva, Switzerland

    Leonardo Pollina, Valeria de Seta, Solaiman Shokur & Silvestro Micera

  2. University Grenoble Alpes, CEA, LETI, Clinatec, Grenoble, France

    Lucas Struber, Serpil Karakas, Stephan Chabardes, Tetiana Aksenova & Guillaume Charvet

  3. Department of Clinical Neuroscience, Lausanne University Hospital, UNIL, Lausanne, Switzerland

    Valeria de Seta

  4. The BioRobotics Institute and Department of Excellence in Robotics and AI, Scuola Superiore Sant’Anna, Pontedera, Italy

    Eleonora Russo, Solaiman Shokur & Silvestro Micera

  5. University Grenoble Alpes, Grenoble University Hospital, Grenoble, France

    Stephan Chabardes

  6. Modular Implantable Neuroprostheses Laboratory, Università Vita-Salute San Raffaele and Scuola Superiore Sant’Anna, Milan, Italy

    Solaiman Shokur & Silvestro Micera

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  1. Leonardo Pollina
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Contributions

L.P., S.S., and S.M. conceptualized the study. L.P., S.S., S.M., L.S., S.K., T.A., S.C., and G.C. designed the task, implemented, and supervised the experimental setup. L.P., L.S., and V.d.S. collected the data. L.P., L.S., V.d.S., and E.R. analyzed the data. All authors participated in the interpretation of the results. L.P., S.S., and S.M. wrote the manuscript with input from all authors.

Corresponding author

Correspondence to Silvestro Micera.

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Pollina, L., Struber, L., de Seta, V. et al. Decoupling simultaneous motor imagination and execution via orthogonal ECoG neural representations. Nat Commun (2026). https://doi.org/10.1038/s41467-026-71234-0

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  • Received: 25 May 2025

  • Accepted: 13 March 2026

  • Published: 31 March 2026

  • DOI: https://doi.org/10.1038/s41467-026-71234-0

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