Evidence map›Paper›PMID 40561476›Full record

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

Corticospinal excitability is facilitated during coordinative action observation and motor imagery.

Ashika Chembila Valappil, Neža Grilc, Federico Castelli, Samantha Chye, David J Wright, Christopher J Tyler, Ryan Knight, Omar S Mian, Neale A Tillin, Adam M Bruton

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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Ashika Chembila ValappilSchool of Life and Health Sciences, Whitelands College, University of Roehampton, Holybourne Avenue, Roehampton, London SW15 4JD, United Kingdom.
Neža GrilcDepartment of Sport, Health and Exercise Sciences, Brunel University of London, Uxbridge UB8 3PH, United Kingdom.
Federico CastelliSchool of Life and Health Sciences, Whitelands College, University of Roehampton, Holybourne Avenue, Roehampton, London SW15 4JD, United Kingdom.
Samantha ChyeSchool of Life and Health Sciences, Whitelands College, University of Roehampton, Holybourne Avenue, Roehampton, London SW15 4JD, United Kingdom.
David J WrightSchool of Psychology, Manchester Metropolitan University, Manchester M15 6BX, United Kingdom.
Christopher J TylerSchool of Life and Health Sciences, Whitelands College, University of Roehampton, Holybourne Avenue, Roehampton, London SW15 4JD, United Kingdom.
Ryan KnightSchool of Life and Health Sciences, Whitelands College, University of Roehampton, Holybourne Avenue, Roehampton, London SW15 4JD, United Kingdom.
Omar S MianSchool of Life and Health Sciences, Whitelands College, University of Roehampton, Holybourne Avenue, Roehampton, London SW15 4JD, United Kingdom.
Neale A TillinSchool of Life and Health Sciences, Whitelands College, University of Roehampton, Holybourne Avenue, Roehampton, London SW15 4JD, United Kingdom.
Adam M BrutonSchool of Life and Health Sciences, Whitelands College, University of Roehampton, Holybourne Avenue, Roehampton, London SW15 4JD, United Kingdom.ORCID 0000-0001-7775-7499

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Combined action observation and motor imagery (AOMI) facilitates corticospinal excitability (CSE). This study used single-pulse transcranial magnetic stimulation (TMS) to explore changes in CSE for coordinative AOMI, where the observed and imagined actions are related but not identical, for a single-leg sit-to-stand (SL-STS) movement. Twenty-one healthy adults completed two testing sessions including baseline (BL), action observation (AO), and motor imagery (MI) control conditions, and three experimental conditions where they observed a slow-paced SL-STS while simultaneously imagining a slow- (AOMIHICO), medium- (AOMIMOCO), or fast-paced (AOMILOCO) SL-STS. A TMS pulse was delivered to the right leg representation of the left primary motor cortex at three stimulation timepoints aligned with peak electromyography (EMG) activity of the knee extensor muscle group for the fast- (T1), medium- (T2), and slow-paced (T3) SL-STS during each condition. Motor evoked potential (MEP) amplitudes were recorded from the knee extensor muscle group as a marker of CSE for all stimulation timepoints and conditions. A main effect for experimental condition was reported for all stimulation timepoints. MEP amplitudes were significantly greater for AOMIHICO at T1 and T3, and AOMIMOCO and AOMILOCO at all stimulation timepoints, when compared with control conditions. This study provides neurophysiological evidence supporting the use of coordinative AOMI.

Indexed as

Evoked Potentials, MotorImaginationMotor CortexPsychomotor PerformancePyramidal TractsAdultElectromyographyFemaleHumansMaleMovementMuscle, SkeletalTranscranial Magnetic StimulationYoung Adultdual-action simulation hypothesismotor evoked potentialmovement simulationtranscranial magnetic stimulationvisual guidance hypothesis

Identifiers

PMID40561476
PMCPMC12192430

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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.