Dissociating neural correlates of action monitoring and metacognition of agency
Open accessAbstract
Judgments of agency refer to people's self-reflective assessments concerning their own control: their assessments of the extent to which they themselves are responsible for an action. These self-reflective metacognitive judgments can be distinguished from action monitoring, which involves the detection of the divergence (or lack of divergence) between observed states and expected states. Presumably, people form judgments of agency by metacognitively reflecting on the output of their action monitoring and then consciously inferring the extent to which they caused the action in question. Although a number of previous imaging studies have been directed at action monitoring, none have assessed judgments of agency as a potentially separate process. The present fMRI study used an agency paradigm that not only allowed us to examine the brain activity associated with action monitoring but that also enabled us to investigate those regions associated with metacognition of agency. Regarding action monitoring, we found that being “out of control” during the task (i.e., detection of a discrepancy between observed and expected states) was associated with increased brain activity in the right TPJ, whereas being “in control” was associated with increased activity in the pre-SMA, rostral cingulate zone, and dorsal striatum (regions linked to self-initiated action). In contrast, when participants made self-reflective metacognitive judgments about the extent of their own control (i.e., judgments of agency) compared with when they made judgments that were not about control (i.e., judgments of performance), increased activity was observed in the anterior PFC, a region associated with self-reflective processing. These results indicate that action monitoring is dissociable from people's conscious self-attributions of control.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The judgment of agency has been linked with activation in the anterior prefrontal cortex, the orbitofrontal cortex, and the fronto-median cortex.
“The judgment of agency has been linked with activation in the anterior prefrontal cortex, the orbitofrontal cortex, the fronto-median cortex (Spengler et al., 2009; Miele et al., 2011; Zito et al., 2020), indicating that this process requires high-order, conceptual mechanisms.”
From The Forward Model: A Unifying Theory for the Role of the Cerebellum in Motor Control and Sense of Agency (2021) · cites this paper as Miele et al., 2011
The fMRI Results (p. 11) report greater activation in the left anterior prefrontal cortex and a right orbitofrontal cluster during judgments of agency than during judgments of performance. The discussion (p. 14) describes these areas as cortical midline structures, but does not report a separate finding of fronto-median cortex activation for agency judgments. (LLM, conf=0.86)
Experimental — accuracy not yet measuredThe DLPFC is associated with metacognition, conscious judgments about the self, and action-selection processes.
“and it was associated with metacognition (Dienes & Perner, 2007), conscious judgments about the self (Miele et al., 2011) and action-selection processes (Haggard, 2017; Perri et al., 2016, 2017).”
From Alteration of hypnotic experience following transcranial electrical stimulation of the left prefrontal cortex (2023) · cites this paper as Miele et al., 2011
The Introduction (p. 3) and “Metacognitive Judgments of Agency: Self-reflective Processing” (p. 14) associate self-reflective judgments with anterior PFC and orbitofrontal cortex activity, but do not establish the claimed association with the DLPFC. The citing sentence attributes metacognition and action-selection processes to other sources, so those are not assessed here. (LLM, conf=0.85)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Meeting of minds: the medial frontal cortex and social cognition
Amodio, D. M., & Frith, C. D. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1884 · Cited by 3,782 · see citing works
Self-referential processing in our brain—A meta-analysis of imaging studies on the self
Northoff, G., Heinzel, A., de Greck, M., Bermpohl, F., Dobrowolny, H., & Panksepp, J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.002 · Cited by 2,792 · see citing works
Dissociable Medial Prefrontal Contributions to Judgments of Similar and Dissimilar Others
Mitchell, J. P., Macrae, C. N., & Banaji, M. R. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.040 · Cited by 1,023 · see citing works
Self-citationDavid, N., Bewernick, B. H., Cohen, M. X., Newen, A., Lux, S., Fink, G. R., Shah, N. J., & Vogeley, K. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2006.18.6.898 · Cited by 252 · see citing works
Evaluating the consistency and specificity of neuroimaging data using meta-analysis
Wager, T. D., Lindquist, M. A., Nichols, T. E., Kober, H., & Van Snellenberg, J. X. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.10.061 · Cited by 242 · see citing works
Self-citationSense of control depends on fluency of action selection, not motor performance
Chambon, V., & Haggard, P. (2012) · Cognition · doi:10.1016/j.cognition.2012.07.011 · Cited by 173 · see citing works
Flagged first, then by citations
Research works printed but not linked: 13
- Blakemore, S. J., Frith, C. D., & Wolpert, D. M. (1999). Spatiotemporal prediction modulates the perception of self-produced stimuli. Journal of Cognitive Neuroscience, 11, 551 -559.
- Franck, N., Farrer, C., Georgieff, N., Marie-Cardine, M., Dalery, J., d ' Amato, T., et al. (2001). Defective recognition of one ' s own actions in patients with schizophrenia. American Journal of Psychiatry, 158, 454 -459.
- Hohwy, J., & Frith, C. (2004). Can neuroscience explain consciousness? Journal of Consciousness Studies, 11, 180 -198.
- Kable, J. W., & Chatterjee, A. (2006). Specificity of action representations in the lateral occipitotemporal cortex. Journal of Cognitive Neuroscience, 18, 1498 -1517.
- Lorch, R., & Myers, J. (1990). Regression analyses of repeated measures data in cognitive research. Journal of Experimental Psychology: Learning, Memory, and Cognition, 16, 149 -157.
- Metcalfe, J., & Greene, M. J. (2007). Metacognition of agency. Journal of Experimental Psychology: General, 136, 184 -199.
- Mulliken, G. H., Musallam, S., & Andersen, R. A. (2008). Forward estimation of movement state in posterior parietal cortex. Proceedings of the National Academy of Sciences, U.S.A., 105, 8170 -8177.
- Pacherie, E. (in press). Sense of agency: Many facets, multiple sources. In H. S. Terrace & J. Metcalfe (Eds.), Agency and joint attention . Oxford, UK: Oxford University Press.
- Powell, L. J., Macrae, C. N., Cloutier, J., Metcalfe, J., & Mitchell, J. P. (2009). Dissociable neural substrates for agentic versus conceptual representations of self. Journal of Cognitive Neuroscience, 22, 2186 -2197.
- Schmitz, T. W., & Johnson, S. C. (2007). Relevance to self: A brief review and framework of neural systems underlying appraisal. Neuroscience & Biobehavioral Reviews, 31, 585 -596.
- van der Meer, L., Costafreda, S., Aleman, A., & David, A. (2010). Self-reflection and the brain: A theoretical review and metaanalysis of neuroimaging studies with implications for schizophrenia. Neuroscience & Biobehavioral Reviews, 34, 935 -946.
- Wegner, D. M. (2002). The illusion of conscious will . Cambridge, MA: MIT Press.
- Wegner, D. M., Sparrow, B., & Winerman, L. (2004). Vicarious agency: Experiencing control over the movements of others. Journal of Personality and Social Psychology, 86, 838 -848.
Cited by
Sorted by citations
An Interoceptive Predictive Coding Model of Conscious Presence
Seth, A. K., Suzuki, K., & Critchley, H. D. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00395 · Cited by 950 · see citing works
“The right angular gyrus of the inferior parietal cortex, and more generally the temporo-parietal-junction, are associated specifically with awareness of the discrepancy between intended and actual movements (Farrer et al., 2008; Miele et al., 2011) and have been implicated in multisensory integration underlying extero…”
BackgroundSmallwood, J. (2013) · Psychological Bulletin · doi:10.1037/a0030010 · Cited by 564 · see citing works
The role of metacognition in human social interactions
Frith, C. D. (2012) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2012.0123 · Cited by 407 · see citing works
Metacognition: computation, biology and function
Fleming, S. M., Dolan, R. J., & Frith, C. D. (2012) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2012.0021 · Cited by 344 · see citing works
The inferior parietal lobule and temporoparietal junction: A network perspective
Igelström, K. M., & Graziano, M. S. A. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.01.001 · Cited by 367 · see citing works
Anatomical coupling between distinct metacognitive systems for memory and visual perception
McCurdy, L. Y., Maniscalco, B., Metcalfe, J., Liu, K. Y., de Lange, F. P., & Lau, H. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1890-12.2013 · Cited by 299 · see citing works
Self-citationNeural responses to heartbeats in the default network encode the self in spontaneous thoughts
Babo-Rebelo, M., Richter, C. G., & Tallon-Baudry, C. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0262-16.2016 · Cited by 207 · see citing works
Sense of control depends on fluency of action selection, not motor performance
Chambon, V., & Haggard, P. (2012) · Cognition · doi:10.1016/j.cognition.2012.07.011 · Cited by 173 · see citing works
Hypnosis and top-down regulation of consciousness
Terhune, D. B., Cleeremans, A., Raz, A., & Lynn, S. J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.02.002 · Cited by 183 · see citing works
Welniarz, Q., Worbe, Y., & Gallea, C. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.644059 · Cited by 125 · see citing works
Neural correlates of sense of agency in motor control: a neuroimaging meta-analysis
Zito, G. A., Wiest, R., & Aybek, S. (2020) · PLOS ONE · doi:10.1371/journal.pone.0234321 · Cited by 79 · see citing works
Metacognition of agency is reduced in high hypnotic suggestibility
Terhune, D. B., & Hedman, L. R. A. (2017) · Cognition · doi:10.1016/j.cognition.2017.06.026 · Cited by 50 · see citing works
Stager, L., Morriss, S., McKibben, L., Grant, M., Szaflarski, J. P., & Fobian, A. D. (2022) · Seizure · doi:10.1016/j.seizure.2022.03.021 · Cited by 21 · see citing works
Perri, R. L., & Di Filippo, G. (2023) · International Journal of Clinical and Health Psychology · doi:10.1016/j.ijchp.2022.100346 · Cited by 21 · see citing works
Effects of explaining a science lesson to others or to oneself: A cognitive neuroscience approach
Zhu, W., Wang, F., Mayer, R. E., & Liu, T. (2024) · Learning and Instruction · doi:10.1016/j.learninstruc.2024.101897 · Cited by 17 · see citing works
Stager, L., Mueller, C., Morriss, S., Szaflarski, J. P., & Fobian, A. D. (2023) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2023.109143 · Cited by 9 · see citing works
A systematic review and meta-analysis on the neural correlates of bodily self-consciousness
Brunello, N., Diana, L., Sritharan, J., Glisic, M., Nef, T., Verma, R. K., & Zito, G. A. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106420 · Cited by 1 · see citing works
- Authors
- Miele, D. B., Wager, T. D., Mitchell, J. P., & Metcalfe, J.
- Affiliations
- Columbia University (US)
- University of Colorado System (US)
- Harvard University (US)
- Venue
- Journal of Cognitive Neuroscience
- Publisher
- MIT Press
- Published
- 2011-11-01
- Volume
- 23
- Issue
- 11
- Pages
- 3620-3636
- ISSN
- 0898-929X (ISSN-L)
- 1530-8898
- OpenAlex
- W2144001056
- Cited by
- 120
- References
- 6
- Citations by year
- 2026: 5 · 2025: 7 · 2024: 8 · 2023: 7 · 2022: 11 · 2021: 7 · 2020: 4 · 2019: 6 · 2018: 1 · 2017: 8 · 2016: 15 · 2015: 7 · 2014: 12 · 2013: 10 · 2012: 9
- FWCI
- 5.34
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Journal of Cognitive Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Columbia Academic Commons (Columbia University)
- Funders
- James S. McDonnell Foundation (220020166)
- University College London
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Free Will and Agency
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Keywords
- action monitoring, perceived control, right temporoparietal junction, pre-supplementary motor area, dorsal striatum, anterior prefrontal cortex, self-initiated action, discrepancy detection
- MeSH terms
- Adolescent, Adult, Analysis of Variance, Brain, Brain Mapping, Cognition, Female, Humans, Image Processing, Computer-Assisted, Judgment, Magnetic Resonance Imaging, Male, Movement, Neuropsychological Tests, Oxygen, Pain Measurement, Reaction Time, Meta-Analysis as Topic, Young Adult
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review