Evidence map›Paper›PMID 41324586›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2025

Learning with others: teacher-learner brain synchrony depends on mutual gaze and joint attention.

Sara De Felice, Francesco Di Ciò, Danny Tompkins, Uzair Hakim, Paola Pinti, Gabriella Vigliocco, Antonia F de C Hamilton

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Behavioral similarity likely drives interbrain neural synchrony.Proceedings of the National Academy of Sciences of the United States of America · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Sara De FeliceDepartment of Psychology, University of Cambridge, Old Cavendish Building, Rayleigh Wing, Free School Lane, CB2 3RF, Cambridge, United Kingdom.ORCID 0000-0003-3065-3363
Francesco Di CiòInstitute of Cognitive Neuroscience, University College London, 17 Queen Square, WC1N 3AZ, London, United Kingdom.
Danny TompkinsInstitute of Cognitive Neuroscience, University College London, 17 Queen Square, WC1N 3AZ, London, United Kingdom.
Uzair HakimDepartment of Medical Physics and Biomedical Engineering, University College London, Malet Place Engineering, Gower St, WC1E 6BT, London, United Kingdom.
Paola PintiCentre for Brain and Cognitive Development, Department of Psychological Sciences, Birbeck, University of London, Henry Wellcome Building, 32 Torrington Square, WC1E 7JL, London, United Kingdom.
Gabriella ViglioccoPsychology and Language Science, University College London, 26 Bedford Way, WC1H 0AP, London, United Kingdom.
Antonia F de C HamiltonInstitute of Cognitive Neuroscience, University College London, 17 Queen Square, WC1N 3AZ, London, United Kingdom.

Funding

ESRC ES/P000592/1European Research Council Advanced Grant 743035Leverhulme DS-2017-026Royal Society Wolfson Research Merit Award WRM\R3\170016UCL Centre for Doctoral Training in Intelligent, Integrated Imaging in Healthcase EP/S021930/1Wellcome TrustWellcome Trust 212979/Z/18/Z
6 · The paper itself

Abstract

Successful learning often emerges through social interaction: what are the neural and behavioral systems that support this process? This ecological, multimodal study combines functional near-infrared spectroscopy hyperscanning with detailed behavioral and physiological measures in 27 unconstrained social learning interactions. Learning was supported by teacher-learner interbrain synchrony (interpersonal neural synchrony), over regions important for mutual understanding (temporoparietal junction) and communicative coordination (ventral premotor cortex). Joint attention and mutual gaze modulated the interpersonal neural synchrony-learning association in oppositive ways, motivating a dual-process model: during knowledge-building phases, learning is supported by informational uptake dynamic, with high joint attention, low interpersonal neural synchrony in regions for mutual understanding (temporoparietal junction) and coordination (right ventral premotor cortex), and high interpersonal neural synchrony in language-related areas (left ventral premotor cortex). In contrast, during moments of mutual grounding, learning is supported by high mutual gaze and high interpersonal neural synchrony over temporoparietal junction. Cross-brain general linear modeling revealed asymmetric neural dependencies linked to speaking and teaching roles in the left-hemisphere language network. These effects remained after controlling for nodding, gaze, and breathing, indicating that interpersonal neural synchrony reflects true social-cognitive alignment beyond sensorimotor coupling. Taken together, this study shows that successful learning arises from coordinated and nonlinear brain-body dynamics and positions interpersonal neural synchrony as a marker of mutual prediction during communicative social interaction.

Indexed as

AttentionBrainFixation, OcularInterpersonal RelationsLearningSocial InteractionAdultBrain MappingFemaleHumansMaleSpectroscopy, Near-InfraredYoung Adultbrain synchronyhyperscanningjoint attentionrelational neurosciencesocial learning

Identifiers

PMID41324586
PMCPMC12667270

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.