Europe PMC

This website requires cookies, and the limited processing of your personal data in order to function. By using the site you are agreeing to this as outlined in our privacy notice and cookie policy.

Abstract 


Some studies showed that a single session of transcranial direct current stimulation (tDCS) has the potential of modulating motor performance in healthy and athletes. To our knowledge, previously published systematic reviews have neither comprehensively investigated the effects of tDCS on athletic performance in both physical and psychological parameters nor investigated the effects of tDCS on high-level athletes. We examined all available research testing a single session of tDCS on strength, endurance, sport-specific performance, emotional states and cognitive performance for better application in competition and pre-competition trainings of national- or international-level athletes. A systematic search was conducted in PubMed, Web of Science, EBSCO, Embase, and Scopus up until to June 2023. Studies were eligible when participants had sports experience at a minimum of state and national level competitions, underwent a single session of tDCS without additional interventions, and received either sham tDCS or no interventions in the control groups. A total of 20 experimental studies (224 participants) were included from 18 articles. The results showed that a single tDCS session improved both physical and psychological parameters in 12 out of the 18 studies. Of these, six refer to the application of tDCS on the motor system (motor cortex, premotor cortex, cerebellum), five on dorsolateral prefrontal cortex and two on temporal cortex. The most sensitive to tDCS are strength, endurance, and emotional states, improved in 67%, 75%, and 75% of studies, respectively. Less than half of the studies showed improvement in sport-specific tasks (40%) and cognitive performance (33%). We suggest that tDCS is an effective tool that can be applied to competition and pre-competition training to improve athletic performance in national- or international-level athletes. Further research would explore various parameters (type of sports, brain regions, stimulation protocol, athlete level, and test tasks) and neural mechanistic studies in improving efficacy of tDCS interventions. Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022326989, identifier CRD42022326989.

Free full text 


Logo of frontphysiolLink to Publisher's site
Front Physiol. 2024; 15: 1365530.
Published online 2024 Jun 19. https://doi.org/10.3389/fphys.2024.1365530
PMCID: PMC11220198
PMID: 38962069

Does a single session of transcranial direct current stimulation enhance both physical and psychological performance in national- or international-level athletes? A systematic review

Ying Yu, , , , , 1 , 2 Xinbi Zhang, , , , 1 , 2 Michael A. Nitsche, , 3 , 4 Carmelo M. Vicario, , , , 5 and Fengxue Qi, , , , , corresponding author 1 , 2 ,*

Associated Data

Data Availability Statement

Abstract

Some studies showed that a single session of transcranial direct current stimulation (tDCS) has the potential of modulating motor performance in healthy and athletes. To our knowledge, previously published systematic reviews have neither comprehensively investigated the effects of tDCS on athletic performance in both physical and psychological parameters nor investigated the effects of tDCS on high-level athletes. We examined all available research testing a single session of tDCS on strength, endurance, sport-specific performance, emotional states and cognitive performance for better application in competition and pre-competition trainings of national- or international-level athletes. A systematic search was conducted in PubMed, Web of Science, EBSCO, Embase, and Scopus up until to June 2023. Studies were eligible when participants had sports experience at a minimum of state and national level competitions, underwent a single session of tDCS without additional interventions, and received either sham tDCS or no interventions in the control groups. A total of 20 experimental studies (224 participants) were included from 18 articles. The results showed that a single tDCS session improved both physical and psychological parameters in 12 out of the 18 studies. Of these, six refer to the application of tDCS on the motor system (motor cortex, premotor cortex, cerebellum), five on dorsolateral prefrontal cortex and two on temporal cortex. The most sensitive to tDCS are strength, endurance, and emotional states, improved in 67%, 75%, and 75% of studies, respectively. Less than half of the studies showed improvement in sport-specific tasks (40%) and cognitive performance (33%). We suggest that tDCS is an effective tool that can be applied to competition and pre-competition training to improve athletic performance in national- or international-level athletes. Further research would explore various parameters (type of sports, brain regions, stimulation protocol, athlete level, and test tasks) and neural mechanistic studies in improving efficacy of tDCS interventions.

Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022326989, identifier CRD42022326989.

Keywords: high-level athletes, physical performance, psychological performance, noninvasive brain stimulation, efficacy

1 Introduction

Athletes undergo systematic training over a long time to improve their athletic performance and achieve superior athletic results in competition. Athletic performance is multifactorial, including both physical and psychological aspects. It requires the development of not only muscular endurance, explosive power, motor coordination and quick and accurate strategic thinking (Colzato et al., 2016), but also stable emotional states and cognitive performance (Hagan et al., 2017). Athletes are often willing to apply top-tier training techniques to enhance athletic performance. Numerous studies have revealed that the brain is crucial for improving athletic performance beyond muscles, heart and lung (Noakes, 2011).

Transcranial direct current stimulation (tDCS) is a non-invasive brain stimulation technique that applies a constant weak direct electrical current using two or more electrodes placed on the scalp to facilitate or inhibit neural activity and/or excitability (Nitsche et al., 2003b). Classically, the effects of tDCS are polarity-dependent in that anodal tDCS (a-tDCS) enhances cortical excitability by subthreshold depolarization of the neural resting membrane potential, and cathodal tDCS (c-tDCS) reduces cortical excitability through hyperpolarization of the neural resting membrane potential (Nitsche and Paulus, 2000; Liebetanz et al., 2002; Stagg and Nitsche, 2011). The after-effects of tDCS last for up to 120 min, or longer, and have been linked to long-term potentiation or long-term depression (Nitsche and Paulus, 2001; Polania et al., 2012; Jamil et al., 2017). Besides, some studies showed that tDCS is an effective method for inducing sustained and widespread changes in regional neural activity and functional connectivity (Lang et al., 2005; Polania et al., 2012). tDCS is widely used in basic research, neuropsychiatric and neurological disorders to modulate cortical excitability, reorganize neuroplasticity, and improve motor performance (Fregni et al., 2006; Angius et al., 2017; Gold and Ciorciari, 2021; Yang et al., 2021; Hou et al., 2022). Therefore, it has attracted the attention of sports scientists. There have been substantial studies showing that tDCS applied over the primary motor cortex (M1), temporal cortex (TC), cerebellum (CB), premotor cortex (PMC) and dorsolateral prefrontal cortex (DLPFC) enhances crucial aspects of motor performance, including muscular strength (Maezawa et al., 2020; Vieira et al., 2020), endurance (Lattari et al., 2016; Ciccone et al., 2019), cognitive control (Wiegand et al., 2019), dynamic balance (Kaminski et al., 2016; Yosephi et al., 2018), and reaction speed (Denis et al., 2019) in healthy people and lower-level athletes.

The effects of tDCS on strength and endurance are more researched, but the results are mixed. The review of Holgado et al. (2019) reported a-tDCS had a small but positive effect on exercise performance, but the effects were not significantly moderated by type of outcome, electrode placement, muscles involved, number of sessions, or intensity and duration of the stimulation. A previous systematic review and meta-analysis reported a-tDCS leads to small and moderate effects on strength (maximal voluntary contraction) and endurance (time to task failure) in healthy young and old adults (Alix-Fages et al., 2019). The review of Machado et al. (2019) reported that a-tDCS but not c-tDCS over M1 improved exercise performance in cycling only in healthy adults. The review of Shyamali Kaushalya et al. (2021) reported that a-tDCS enhance running and cycling time in time to exhaustion tasks but no improved in endurance time trial or sprint tasks in healthy people. The review of Chinzara et al. (2022) reported that tDCS has the potential to be used as an ergogenic aid in physical endurance, muscular strength, and visuomotor skills in healthy adults. This controversy in reviews might be attributed to different brain region targets, stimulation protocols, test tasks, and motor abilities in participants.

Some studies showed that tDCS effectively improves sport-specific performance, such as golf putting (Zhu et al., 2015) and basketball performance (shooting precision, specific dribbling, and agility) in healthy people (Veldema et al., 2021). A recent systematic review and meta-analysis reported that a single anodal tDCS session can enhance sport-specific motor performance in healthy adult athletes who have been regularly participating in organized sports for at least 2 years (Maudrich et al., 2022). However, some studies yielded inconsistent results (Valenzuela et al., 2019; Penna et al., 2021; Moreira et al., 2022). Achieving high-level of athletic performance is often believed to demand a minimum of a decade or 10,000 h of practice, based on the time dedicated to practicing a task (Ericsson KA and Tesch-Römer, 1993). According to McKay et al. (McKay et al., 2022) ‘s classification of sports levels, athletes above tier 3 (Highly Trained/National Level, Elite/International Level and World Class) in studies could provide reliable performance outcomes and suited to both laboratory- and field-based research. The brains of high-level athletes have different characteristics compared with the general population and lower-level athletes (Nakata et al., 2010), such as higher neural excitability (Wright et al., 2010; Callan and Naito, 2014; Monda et al., 2017) and specific neural responses during exercise (Del Percio et al., 2010; Casanova et al., 2013; Ermutlu et al., 2015). Whether a single session of tDCS can apply to competition and pre-competition training in national- or international-level athletes remains uncertain. More importantly, psychological parameters such as emotional state and cognitive performance are important for athletic performance under intense conditions (Hagan et al., 2017; Valenzuela et al., 2019; Fortes et al., 2022). Emotional state had proven a relationship with athletic performance and change of sporting success (Zandi and Rad, 2013; Brandt et al., 2017). Cognitive performance such as inhibitory control, visual search and decision-making are crucial for accuracy and consistency of movements, as well as efficiently processing the surrounding information to adopt the correct action in a given situation (Chiu et al., 2017). Yet previous review studies focused only on the effects of tDCS on motor and sport-specific performance in healthy people and athletes of all levels, with less attention paid to cognitive performance and emotional states. Whether a single session of tDCS improved athletic performance in high-level athletes and in what aspects it is effective is still inconclusive. Therefore, we carried out a systematic review to comprehensively analyze the effects of a single session of tDCS on athletic performance in strength, endurance, sport-specific performance, emotional states and cognitive performance in national- or international-level athletes, in order to improve the efficacy of tDCS on high-level athletes.

2 Methods

A systematic literature review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (Liberati et al., 2009). Details of the review protocol were registered on PROSPERO on April 2022 (CRD42022326989). A meta-analysis was not conducted due to high measurement and methodological heterogeneity in the selected studies.

2.1 Literature search

The literature search was performed until June 2023 by two independent researchers (Y.Y., Z.X.B.) using the PubMed, Web of Science, EBSCO, Embase, and Scopus databases, and the keywords (“tDCS” OR “transcranial Direct Current Stimulation”) AND (“athlete” OR “player” OR “sport” OR “athletic performance” OR “psychological performance” OR “physical performance” OR “cognitive performance” OR “cognitive function”). Additional relevant studies were also scanned in the references of the retrieved literature to broaden the search.

2.2 Study inclusion and exclusion criteria

Studies were included according to the “participants, intervention, comparator, outcomes, study design” inclusion criteria: 1) healthy athletes in highly trained/national level and elite/international level (McKay et al., 2022); 2) intervention consisting of a single tDCS session; 3) sham tDCS or no interventions as control groups; 4) inclusion of all detailed test results; and 5) randomized controlled trials with crossover or parallel group designs.

The exclusion criteria were: 1) no specification of the level of athletes; 2) other interventions during the experiment; and 3) non-English language, review papers, conference abstracts, study protocols, and papers without relevant experimental data.

2.3 Study selection and risk-of-bias assessment

The literature screening was conducted independently by two researchers based on the inclusion and exclusion criteria. A third researcher was consulted in case of disagreement. The Cochrane Risk of Bias assessment tool assessed bias in the included studies (Habay et al., 2021). Quality assessment included random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, incomplete outcome data bias, selective reporting, and other biases. Each component was rated as having a “high”, “low”, or “unclear” risk of bias. The Review Manager 5.4.1 software (Cochrane Collaboration, Oxford, UK) was used.

3 Results

3.1 Search results

A total of 589 articles (PubMed, 208; Web of Science, 92; EBSCO, 87; Embase, 70; Scopus, 130; other sources, 2) were found in the systematic literature search. After the removal of duplicate articles, 330 articles were screened based on their title and abstract, of which 266 articles were excluded. After full-text assessment, 47 records were excluded. Finally, 18 articles were eligible for the systematic review. The literature search process is shown in Figure 1.

3.2 Quality and risk-of-bias assessment

The overall quality of the included studies was high, with all studies using a randomized controlled experimental design. However, 12 of the included studies showed an unclear risk of selection bias, due to unclear random sequence generation in 10 articles and unclear allocation concealment in six articles. One study showed an unclear risk with respect to blinding of outcome assessment. Four studies showed an unclear risk of other biases. The risk-of-bias graphs and a summary are presented in Figure 2.

An external file that holds a picture, illustration, etc.
Object name is fphys-15-1365530-g002.jpg

Quality and risk-of-bias assessment. Risk of bias graph (A): review authors’ judgments about each risk of bias item presented as percentages across all included studies; and risk of bias summary (B): review authors’ judgments about each risk of bias item for each included study.

3.3 Study characteristics and result synthesis

An overview of literature characteristics is given in Table 1. All studies used crossover designs with a sham condition as a comparator. In total, 224 athletes were included in 18 studies, with 156 men (69.64%) and 68 women (30.36%). The mean age of the participants ranged from 16.10 ± 0.90 years (Vargas et al., 2018) to 33.00 ± 9.00 years (Okano et al., 2015). The average age of the subjects in one study conducted by Liang et al. (2022) was unknown. All studies used sham tDCS as a control condition. The studies covered handball, soccer, shooting, swimming, basketball, gymnastic, volleyball, triathlon, rowing, taekwondo, archery, and cycling. All subjects had sports experience at least state- and national-level competitions. All experimental groups used a-tDCS, while two studies used both, anodal/cathodal stimulation (Mehrsafar et al., 2020; Salehi et al., 2022). With the exception of eight studies applying a cephalic montage of the return electrode, all examined studies applied an extracephalic montage of the return electrode. Regarding the tDCS application protocol, all studies opted for the offline modality (testing after stimulation), with five studies including also the online stimulation modality (testing during stimulation) (Hazime et al., 2017; Vargas et al., 2018; Fortes et al., 2022; Moreira et al., 2022; Anoushiravani et al., 2023). Three studies out of 18 studies did not measure side effects of the tDCS intervention. None of the studies reported any adverse effects or injuries after the intervention and the common sensations were itching and tingling. The basic characteristics of the literature are shown in Tables 1, ,22.

TABLE 1

Characteristics of the studies.

ReferencesSportsGenderAgeSports experienceTimingModelDesign
Okano et al. (2015) Cycling10M33.00 ± 9.00Nation levelOfflinea-tDCSCrossover
Hazime et al. (2017) Handball8F19.65 ± 2.55State and national competitionsOnline/Offlinea-tDCSCrossover
Mesquita et al. (2019a) Taekwondo12M7F19.00 ± 3.00Nation levelOfflinea-tDCSCrossover
Vargas et al. (2018) Soccer20F16.10 ± 0.90State and national competitionsOnline/Offlinea-tDCSCrossover
Valenzuela et al. (2019) Triathlon8M22.00 ± 2.00International competitionsOfflinea-tDCSCrossover
Mesquita et al. (2020) Taekwondo8M4F19.00National or international tournamentsOfflinea-tDCSCrossover
Mehrsafar et al. (2020) Archery12M26.51 ± 2.31National levelOfflinea/c-tDCSCrossover
Moreira et al. (2021) Soccer12M19.00 ± 1.00Professional Football Club PlayersOfflinea-tDCSCrossover
Pollastri et al. (2021) Cycling8M20.00 ± 1.50International competitionsOfflinea-tDCSCrossover
Machado et al. (2021) Cycling, Rowing12M29.40 ± 7.30State, national or world-class competitionsOfflinea-tDCSCrossover
Salehi et al. (2022) Swimming15M23.00 ± 1.00State and national competitionsOfflinea/c-tDCSCrossover
Penna et al. (2021) Swimming10M30.00 ± 6.00National levelOfflinea-tDCSCrossover
Liang et al. (2022) Rowing8FNRNational levelOfflinea-tDCSCrossover
Park et al. (2022) Volleyball13F21.92 ± 2.81Professional Volleyball Club PlayersOfflinea-tDCSCrossover
Moreira et al. (2022) Basketball8F25.00 ± 8.00Professional Basketball PlayersOnline/Offlinea-tDCSCrossover
Gallo et al. (2022) Cycling12M21.3 ± 4.30Nation levelOfflinea-tDCSCrossover
Fortes et al. (2022a) Basketball20M24.77 ± 4.2National levelOnline/Offlinea-tDCSCrossover
Anoushiravani et al. (2023) Gymnastic17M21.05 ± 2.04National competitionsOnline/Offlinea-tDCSCrossover

Abbreviations: M = male; F = female; NR, not reported; a-tDCS, anodal tDCS; c-tDCS, cathodal tDCS.

TABLE 2

Overview of studies investigating a single session of transcranial direct current stimulation for improving athletic performance in elite athletes.

ReferencesStimulus(S) Reference(R)Electrode size [cm2]Intensity [mA]Duration [mins]IndicatorsMain outcomes
Strength
Hazime et al.S:M1 (C3 or C4) R:IOCS = R = 352.020MVICa-tDCS improved MVIC of shoulder rotator
Vargas et al.S:M1 (C3 or C4) R:COCS = R = 352.020MVICa-tDCS improved MVIC of external and internal knee extensor
Mesquita et al.S:Bilateral M1 (C3, C4) R:ISS = 35 R = 251.515CMJNo significant difference in CMJ
Park et al.S:M1 (Cz) R:M1 (C5, C6)S = R = 282.0201RM, CMJNo significant difference in CMJ, bench-press and back-squat 1 RM
Anoushiravani et al.S: Bilateral PMC R: COCS = R = 352.020BJT, MVICa-tDCS improved BJT, MVIC of all upper body muscles
S: Bilateral CB R: COCS = R = 352.020a-tDCS improved MVIC of right deltoid and trapezius, left biceps and pectoralis muscle
Endurance
Okano et al.S:Left TC (T3) R:COCS = R = 352.020MITa-tDCS improved PPO
Pollastri et al.S:Bilateral DLPFC (F3, F4) R:Fp1, F7, C3, Fp2, F8, C4S = R = 3.141.52015 km TTa-tDCS improved PPO and total time
Machado et al.S:M1 (Cz, C1, C2) R:C3, C4, FC1, FC2, P1, P2NR2.420TTE at 80% PPONo significant difference
S:M1 (Cz) R: Occipital protuberanceS = 36 R = 352.020
Gallo et al.S:Bilateral DLPFC (F3, F4) R:Fp1, F7, C3, Fp2, F8, C4S = R = 3.141.5202 km TTa-tDCS improved total time
Sport-specific performance
Salehi et al.S:Left DLPFC (F3) R:COC (Fp2)S = R = 352.02050-m swimming testa-tDCS improved total time
Valenzuela et al.S:M1 (C3) R:COC (Fp2)S = R = 252.020800-m swimming testNo significant difference
Penna et al.S:Left TC (T3) R:ISS = R = 352.030800-m swimming testNo significant difference
Moreira et al.S:Left DLPFC (F3) R:Right DLPFC (F4)S = R = 352.020Shooting taskNo significant difference
Liang et al.S:M1 (Cz) R:C5, C6S = R = 242.2205 km rowingNo significant difference in speed and power
Mesquita et al.S:Bilateral M1 (C3, C4) R:ISS = 35 R = 251.515FSKTa-tDCS worsens the total number of kicks
Park et al.S:M1 (Cz) R:C5, C6S = R = 282.020Spike taska-tDCS improved spike speed
Mesquita et al.S:Bilateral M1 (C3, C4) R:ISS = 35 R = 251.515PSTTNo significant difference in kicking frequency
Anoushiravani et al.S: Bilateral PMC R: COCS = R = 352.020BHST, SLHT,DLCT, ASFT,SRT,DPBTa-tDCS improved SLHT, BHST, DPBT
S: Bilateral CB R: COCS = R = 352.020a-tDCS improved SLHT
Emotional state
Valenzuela et al.S:M1 (C3) R:COC (Fp2)S = R = 252.020BMSa-tDCS improved vigor
Mehrsafar et al.S:Left DLPFC (F3) R:Right DLPFC (F4)S = R = 252.020BMS, CSAI-2a-tDCS improved vigor, decreased tension, fatigue and anxiety
Moreira et al.S:Left DLPFC (F3) R:Right DLPFC (F4)S = R = 352.020WBQa-tDCS improved total score
Machado et al.S:M1 (Cz, C1, C2) R:C3, C4, FC1, FC2, P1, P2NR2.420BMSNo significant difference in total score
S:M1 (Cz) R: Occipital protuberanceS = 36 R = 352.020
Cognitive performance
Moreira et al.S:Left DLPFC (F3) R:Right DLPFC (F4)S = R = 352.020Stroop taskNo significant difference in RT and accuracy
Gallo et al.S:Bilateral DLPFC (F3, F4) R:Fp1, F7, C3, Fp2, F8, C4S = R = 3.141.520Stroop taskNo significant difference in RT and accuracy
Fortes et al.S:Middle TC (CP5) R:Visual cortex (Oz)S = R = 252.030Visuomotor task Decision-makinga-tDCS improved RT and accuracy in decision-making, and RT in visuomotor task

The effects of tDCS on improving athletic performance were categorized into strength, endurance, sport-specific performance, emotional states, and cognitive performance. Abbreviations: a-tDCS, anodal tDCS; FSKT, frequency speed of kick test; PSTT, progressive specific taekwondo test; MVIC, maximal voluntary isometric contraction; CMJ, countermovement jump; TTE, time to exhausted test; MIT, maximal incremental test; TT, time trail; PPO, peak power output; 1RM, 1 repetition maximum; BJT, broad jump test; SLHT, straddle lift to handstand test; DLCT, double legs circle test; BHST, back hang scale test; ASFT, active shoulder flexibility test; SRT, sit and reach test; DPBT, dips on parallel bars test; WBQ, Wellbeing Questionnaire; BMS, brunel mood scale; CSAI-2, competitive state anxiety inventory second edition; RT, reaction time; cm2 = square centimeter; mA = milliamps; mins, minutes; M1 = primary motor cortex; DLPFC, dorsolateral prefrontal cortex; TC, temporal cortex; PMC, premotor cortex; CB, cerebellum; COC, contralateral orbitofrontal cortex; IOC, ipsilateral orbitofrontal cortex; IS, ipsilateral shoulder; S = stimulating electrode; R = reference electrode; NR, not reported; F = female; M = male.

These studies contained five stimulation regions: M1 (44.44%), DLPFC (33.33%), PMC (5.5%), CB (5.5%), and TC (16.67%). Five studies used bilateral anodal stimulation protocols (Mesquita et al., 2019b; Mesquita et al., 2020; Pollastri et al., 2021; Gallo et al., 2022; Anoushiravani et al., 2023), and the remaining studies used unilateral stimulation. Three studies used high-definition tDCS (HD-tDCS), and the other studies used a conventional tDCS setup using two electrodes (anode and cathode). Regarding the HD-tDCS setups, two used two sets of 3 × 1 electrodes (i.e., one anode and three cathodes) with 3.14-cm2 circular electrodes (Pollastri et al., 2021; Gallo et al., 2022), and Machado et al. (Machado et al., 2021) adopted a 6 × 3 (i.e., three anodes and six cathodes) ring configuration. Studies used stimulation durations of 15–30 min. The current intensity was 1.5 mA (Pollastri et al., 2021), 2.0 mA (Okano et al., 2015; Hazime et al., 2017; Vargas et al., 2018; Valenzuela et al., 2019; Mesquita et al., 2020; Machado et al., 2021; Penna et al., 2021; Moreira et al., 2022; Park et al., 2022; Salehi et al., 2022; Anoushiravani et al., 2023), 2.2 mA (Liang et al., 2022), and 2.4 mA (Machado et al., 2021). The electrode size varied between 3.14 cm2 and 36 cm2. The electrode size for HD-tDCS in the study by Machado et al. (2021) was not reported. The stimulation times, sites, and current intensities are shown in Figure 3.

An external file that holds a picture, illustration, etc.
Object name is fphys-15-1365530-g003.jpg

Visualization of stimulated time, site, current intensity and performance in the analyzed studies. The color bars represent athletic performance involved in analyzed studies.

The effects of tDCS on improving athletic performance were categorized into the following domains: strength (5 studies), endurance (4 studies), sport-specific performance (9 studies), emotional states (4 studies), and cognitive performance (3 studies).

Regarding muscle strength measurements, five studies used maximal voluntary isometric contraction (MVIC), the countermovement jump test (CMJ), broad jump test (BJT), and one-repetition maximum loads to measure the effects of tDCS in soccer, handball, taekwondo, gymnastic, and volleyball athletes (Hazime et al., 2017; Vargas et al., 2018; Mesquita et al., 2019a; Park et al., 2022; Anoushiravani et al., 2023). Among them, three studies (60%) found improvements. Vargas et al. (2018) and Hazime et al. (2017) found that 2-mA a-tDCS (0.0571 mA/cm2) over M1 (electrodes C3 or C4; International 10–20 System) for 20 min improved the MVIC of knee extensors in soccer players and external and internal shoulder rotators in handball players during stimulation, these effects lasted for 60 min. Anoushiravani et al. (2023) reported that 2-mA a-tDCS (0.0571 mA/cm2) improved BJT performance and MVIC of all tested upper body muscles when applied over the PMC for 20 min, and MVIC of the right deltoid and trapezius, and left biceps and pectoralis muscles when applied over the CB for 20 min. Park et al. (2022) reported no significant improvements of CMJ performance, bench press performance, and back squat one-repetition maximum loads in volleyball players by 2-mA a-tDCS (0.0714 mA/cm2) over M1 (Cz) for 20 min. Mesquita et al. (2019a) found that 1.5-mA a-tDCS (0.0428 mA/cm2) for 15 min applied over M1 bilaterally (C3 and C4) did not have significant improving effects on CMJ performance in taekwondo athletes.

Regarding endurance performance, four studies used peak power output (PPO) and the time in time-to-exhaustion test (TTE), time trial test (TT), or maximal incremental test (MIT) to assess the effects of tDCS in cyclists and rowers (Okano et al., 2015; Machado et al., 2021; Pollastri et al., 2021; Gallo et al., 2022). Among these studies, three (75%) reported positive influences. Okano et al. (Okano et al., 2015) showed that 2-mA a-tDCS (0.0571 mA/cm2) applied over the left TC (T3) for 20 min increased PPO in the MIT in cyclists. Gallo et al. and Pollastri et al. applied 1.5-mA HD-tDCS (0.238 mA/cm2) over the bilateral DLPFC (F3 and F4) for 20 min, and this stimulation protocol improved total time in 2-km TT, PPO and total time in 15-km PPO in cyclists compared with sham stimulation (Pollastri et al., 2021; Gallo et al., 2022). Machado et al. (2021) however report that neither 2.4-mA HD-tDCS over the M1 (Cz, C1, and C2) for 20 min nor 2-mA conventional a-tDCS over M1 (Cz) for 20 min affected total time in TTE at 80% PPO in cyclists and rowers compared with sham stimulation. The authors did not report the electrode sizes used for HD-tDCS, and the stimulus and reference electrode current densities were 0.055 mA/cm2 and 0.0571 mA/cm2, respectively, for conventional tDCS.

Regarding sport-specific performance, the test parameters in the nine studies included swimming speed (50 m and 800 m), 5 km rowing, basketball shooting accuracy, volleyball spike performance, gymnastic performance, the Progressive Specific Taekwondo Test, and the Taekwondo frequency speed of kick test (Mesquita et al., 2019b; Valenzuela et al., 2019; Mesquita et al., 2020; Penna et al., 2021; Liang et al., 2022; Moreira et al., 2022; Park et al., 2022; Salehi et al., 2022). Among them, only three studies reported positive effects of tDCS. Salehi et al. (2022) reported that 2-mA a-tDCS (0.0571 mA/cm2) applied over the left DLPFC (F3) for 20 min improved 50-m swimming speed in professional swimmers. Moreira et al. (2022) used identical tDCS parameters and found however no effects on shooting accuracy in basketball players. Moreover, neither Valenzuela et al.nor Penna et al. found improvements in the 800-m swimming test using 2-mA a-tDCS over M1 (C3) for 20 min and left TC (T3) for 30 min (Valenzuela et al., 2019; Penna et al., 2021). Park et al. (2022) showed that 2-mA a-tDCS (0.0714 mA/cm2) over M1 (Cz) for 20 min improved volleyball spike speed and consistency compared with sham stimulation. Mesquita et al. (2019b; 2020) reported that 1.5-mA a-tDCS over the bilateral M1 (C3 and C4) for 15 min did not improve performance of the Progressive Specific Taekwondo Test and worsened performance on the frequency speed of kick test in taekwondo athletes. Similarly, Liang et al. (2022) showed that 2.2-mA a-tDCS over M1 (Cz) for 20 min did not increase 5-km rowing speed. Anoushiravani et al. (2023) reported that 2-mA a-tDCS over the PMC for 20 min improved performance on the straddle lift to handstand test, back hang scale test, and dips on parallel bars test and that 2-mA a-tDCS over the CB for 20 min improved straddle lift to handstand test performance in gymnastic athletes.

Four studies investigated the effects of tDCS on emotional states, with testing parameters including the Brunel Mood Scale, Competitive State Anxiety Inventory Second Edition, and Well-Being Questionnaire in archers, soccer players, triathletes, cyclists, and rowers (Valenzuela et al., 2019; Mehrsafar et al., 2020; Machado et al., 2021; Moreira et al., 2021). Among these studies, three reported positive results. Mehrsafar et al. found that 2-mA (0.08 mA/cm2) a-tDCS over the left DLPFC (F3) for 20 min improved vigor and reduced tension and anxiety in archers (Mehrsafar et al., 2020). Moreira et al. (2021) used the same tDCS parameters and found that a-tDCS (0.0571 mA/cm2) improved wellbeing in soccer players after a match. Still, there were inconsistent results regarding the effects of tDCS applied over the M1 on emotional states. Valenzuela et al. (2019) showed that 2-mA a-tDCS over the M1 (C3) for 20 min improved the vigor of triathletes compared with sham stimulation. Machado et al. (2021) found that neither HD-tDCS nor conventional a-tDCS over M1 improved Brunel Mood Scale scores in cyclists and rowers.

Three studies investigated the effects of tDCS on cognitive performance using reaction time (RT) and accuracy in the Stroop task (Okano et al., 2015; Penna et al., 2021), visuomotor skill and decision-making task (Fortes et al., 2022) in basketball players and cyclists. Among them, one study reported positive results. Fortes et al. (2022) found that 2 mA a-tDCS (0.08 mA/cm2) over the middle TC (CP5) for 30 min improved RT and accuracy in visuomotor skills as well as RT in decision-making in basketball players. Moreira et al. (2022) did not find improvements in Stroop task RT and accuracy in basketball players using 2-mA a-tDCS over the left DLPFC (F3) for 20 min. Moreover, Gallo et al. (2022) showed that 1.5-mA HD-tDCS over the bilateral DLPFC (F3 and F4) for 20 min did not improve Stroop task RT and accuracy in cyclists.

4 Discussion

In the present study, we performed a systematic review of the literature on the effects of a single session of tDCS in national- or international-level athletes. Numerous studies and reviews have investigated the effects of tDCS on exercise performance such as strength and endurance in individuals with motor impairments and in healthy individuals (Alix-Fages et al., 2019; Holgado et al., 2019; Morya et al., 2019; Patel et al., 2019; Chinzara et al., 2022; Marinus et al., 2022), but the number of studies on athletes, particularly national- or international-level athletes, is limited. A recent systematic review and meta-analysis investigated a single anodal tDCS session on sport-specific motor performance in athletes participating regularly for at least 2 years (Maudrich et al., 2022). As far as we know, no reviews study has comprehensively investigated the effects of tDCS on athletic performance in both physical and psychological parameters in high-level athletes. Our studies included high-level athletes at tiers 3 (highly trained/national level) and four (international level), based on a recently proposed participant classification framework (McKay et al., 2022). Therefore, we examined 18 studies, involving 224 subjects in 12 sports disciplines. Our analysis showed that a single session of 1.5–2.4-mA tDCS with a duration of 15–30 min resulted in heterogeneous outcomes. The most sensitive to tDCS are strength (improvement in 67% of studies), endurance (improvement in 75% of studies), and emotional states (improvement in 75% of studies). It is interesting to note that the positive effects of tDCS on performance are significantly reduced in the case of sport-specific tasks (40% of studies) and cognitive performance (33% of studies). This suggests that tDCS is a promising tool to improve sportive performance but that it is more effective in no task specific aspects of athletic performance. More importantly, this is the first systematic review to analyze the effects of tDCS on emotional states and cognitive performance in high-level athletes. Emotional state and cognitive performance are crucial for athletic performance under intense conditions. Our analysis showed that tDCS can modulate emotional states, such as improving vigor and decreasing tension, fatigue, and anxiety, as well as cognitive performance, such as improving reaction time and accuracy in decision-making. However, research on the effects of tDCS on emotional states and cognitive performance is relatively sparse. Both of these are key focus points for future research.

tDCS applied to specific brain regions can induce particular neuromodulatory processes (Machado et al., 2021). Through complex networks and systems, several brain areas regulate or promote athletic performance, including the M1, PMC, CB, DLPFC and TC. M1 plays a crucial role in athletic performance, however results with tDCS applied over M1 were inconsistent (Edwards et al., 2017; Machado et al., 2019; Shyamali Kaushalya et al., 2021). Machado et al. (2019) reported that a-tDCS over M1 improved exercise performance in cycling only in healthy adults. Among the seven studies applying tDCS over M1, four showed improvements in muscle strength, sport-specific performance, and emotional states. Regarding muscle strength performance, two studies showed that a-tDCS (2 mA, 20 min) over M1 (C3 or C4) increased the MVIC in handball and football athletes (Hazime et al., 2017; Vargas et al., 2018). tDCS over M1 can enhance corticospinal excitability to alter motor unit firing and muscle recruitment strategies (Krishnan et al., 2014; Dutta et al., 2015; Polania et al., 2018). Regarding sport-specific performance, Park et al. (2022) showed improved volleyball spike speed and consistency using a-tDCS (2 mA, 20 min) over M1. Spike performance is closely related to coordination patterns and muscle synergies of the entire body (Wagner et al., 2014). Veldema et al. (2021) reported that 1-mA a-tDCS over M1 for 20 min improved basketball shooting performance in healthy sports students. This implies that tDCS may have positive effects on specific motor coordination in high-level athletes. In addition, tDCS over M1 may potentially increase explosive force (Lu et al., 2021), as shown for volleyball spike speed. Regarding emotional states, Valenzuela et al. (2019) used 2-mA a-tDCS for 20 min over the M1 and improved vigor in triathletes. A previous study found that tDCS over M1 (C3) improved mood in patients with fibromyalgia, which may be related to elevated serum beta-endorphin levels (Khedr et al., 2017). tDCS has been observed to alter activation and functional connectivity of the region under the anode. Additionally, the conventional method using two large sponge pad electrodes was found to affect the functional connectivity of other cortical and deep brain regions, particularly in the DLPFC (van den Heuvel and Sporns, 2013; To et al., 2018; Piretti et al., 2022). The activation of the DLPFC has been linked to improvements in mood states (Ligeza et al., 2021). Hence, tDCS applied over the M1 likely alter activation and functional connectivity of the DLPFC, potentially causing the observed augmentations in mood after tDCS.

Some studies however report no difference in neuromuscular or sport-specific performance between M1-tDCS and sham stimulation (Mesquita et al., 2019b; Valenzuela et al., 2019; Machado et al., 2021; Liang et al., 2022; Park et al., 2022), suggesting that tDCS over the M1 may not affect sport-specific movement patterns in high-level athletes in each case, and that facilitation of cortical excitability does not always induce improvements in athletic performance in high-level athletes. The brains of high-level athletes show specific neural responses during exercise compared to the general population and non-elite athletes (Del Percio et al., 2010; Nakata et al., 2010; Wright et al., 2010; Casanova et al., 2013; Callan and Naito, 2014; Ermutlu et al., 2015; Monda et al., 2017). Long-term training may develop specialized neural networks that implement the automatic execution of movements and reduce neural activity in high-level athletes (Xu et al., 2016; Guo et al., 2017). These findings are in line with the “neural efficiency” hypothesis, which suggests more efficient cortical functions in more skilled individuals, requiring less cortical activation (Del Percio et al., 2008; Babiloni et al., 2010; Dunst et al., 2014). On the other hand, high-level athletes showed higher baseline levels of neural excitability and brain-derived neurotrophic factor concentration compared to healthy non-athletes (Al-Khelaifi et al., 2018; Donati et al., 2021). Although the exact mechanisms underlying these effects have not been clarified in detail, some studies have shown that tDCS can affect neural excitability and neural plasticity through reducing gamma-aminobutyric acid inhibition and increasing brain-derived neurotrophic factor levels (Liebetanz et al., 2002; Nitsche et al., 2003a; Frazer et al., 2016). Thus, tDCS may not affect on neural excitability and plasticity in high-level athletes. Mesquita et al. (2019b) reported that 1.5-mA a-tDCS over the bilateral M1 for 15 min did not enhance kick frequency in 19 black-belt taekwondo athletes and reduced the total number of kicks compared to a control group. This implied that bilateral M1 stimulation worse performance than unilateral stimulation. This discrepancy may be explained by current flow direction. A recent study reported that corticospinal excitability was decreased after a-tDCS over bilateral M1 in healthy adults (Behrangrad et al., 2022). Studies investigating the effects of tDCS on neural excitability in athletes are scarce. Future research should focus on neural mechanistic studies to elucidate the impact of various protocols and target brain areas of tDCS on high-level athletes.

The PMC forms an important node in frontoparietal networks and contributes to specification of movement parameters (Kantak et al., 2012). One study found that 2-mA a-tDCS over the PMC for 20 min improved MVIC of all upper body muscles and gymnastic performance in gymnastic athletes (Anoushiravani et al., 2023). A recent study showed that a-tDCS over PMC improved functional connectivity within PMC and between PMC and M1, and enhanced motor performance after stroke (Unger et al., 2023). This implies that PMC activation via tDCS could enhance motor network activity and premotor-motor functional connectivity, and result in performance improvements. Further, the CB is an important node in motor control and coordination of complex movements (Jacobs and Horak, 2007). One study found that 2-mA a-tDCS over the CB for 20 min improved MVIC of the right deltoid and trapezius and left biceps and pectoralis muscles and straddle lift to handstand test in gymnastic athletes (Anoushiravani et al., 2023). Kenville et al. (2020) showed that 2-mA tDCS over CB for 20 min improved MVIC during isometric barbell squats in healthy individuals. Studies showed enhanced connectivity in fronto-parietal-cerebellar networks and motor cortex-cerebellar networks following motor adaptation in healthy subjects (Sami and Miall, 2013; Vahdat et al., 2014). tDCS over CB has potential benefits for motor tasks and improves locomotor performance, and tDCS can increase postural control by affecting connections between the CB and M1 and influencing the function of the vermis (Celnik, 2015). There are inhibitory interactions between the CB and M1, which may have limited the effects of tDCS over CB. According to the latest finding, a-tDCS over right CB increased cerebellar brain inhibition and reduced M1 excitability (Galea et al., 2009). Behrangrad et al. found that bilateral a-tDCS over the M1 + CB and bilateral a-tDCS over the CB significantly increased corticospinal excitability (Behrangrad et al., 2022). It seems that the stimulation protocol affects the effects of tDCS over CB on neural excitability and muscle strength enhancement and this should be investigated in future studies.

Five studies included in this review investigated the effects of tDCS applied over the DLPFC on endurance, emotional states, and cognitive performance. Regarding endurance, two studies reported that 1.5-mA HD-tDCS over the bilateral DLPFC (F3 andF4) for 20 min improved total time required for in 2-km TT, PPO and total time required for 15 km distance in cyclists compared with sham stimulation (Pollastri et al., 2021; Gallo et al., 2022). It was reported that 1.5-mA HD-tDCS over the bilateral DLPFC (F3 and F4) for 20 min delayed the increase in ratings of perceived exertion (RPE) during TT and lead to higher power output at the same RPE compared with sham stimulation (Pollastri et al., 2021). The main function of the DLPFC is executive control of behavior (Miller and Cohen, 2001), a-tDCS over DLPFC demonstrated an increase in resting functional connectivity within networks including the DLPFC (Keeser et al., 2011) and increased coupling between the left and right DLPFC and the left sensorimotor cortex (Stagg et al., 2013). A recent study showed that 2-mA a-tDCS over the left DLPFC for 30 min delayed TTE, reduced the heart rate and RPE, and improved Stroop task performance in healthy individuals (Angius et al., 2019). tDCS over the left DLPFC enhances endurance performance, improves inhibitory control, and reduces the perception of effort by enhancing neural activity (Maeoka et al., 2012). Regarding emotional states, Moreira et al. (2021) reported that 2-mA a-tDCS over the left DLPFC for 20 min improved wellbeing scores in soccer players in real competition. Mehrsafar et al. (2020) found that a-tDCS enhanced vigor and reduced tension and pre-competition anxiety in archers. The activation of the prefrontal cortex has been associated with improvements in mood states (Ligeza et al., 2021; Park et al., 2021). It reported that tDCS over left DLPFC promote the descending pain inhibitory system by enhancing neural activity (Maeoka et al., 2012). However, two studies found that tDCS over DLPFC did not improve Stroop task performance in basketball players and cyclists (Gallo et al., 2022; Moreira et al., 2022). The Stroop paradigm is a valid indicator of inhibitory function. Inhibitory control is associated with the exclusion of irrelevant information or behavioral distractions and avoiding errors (Engle, 2016), affecting anticipation and decision-making during competition (Wood et al., 2016). Athletes demonstrate significantly higher cognitive performance than the general population (Nakamoto and Mori, 2008; Post et al., 2009; Irwin et al., 2011; Smith et al., 2016; Andrade et al., 2020). The “neural efficiency” hypothesis proposes that high-level athletes have lower brain activation during simple tasks and only show higher brain activation when performing difficult tasks (Del Percio et al., 2010). Simple cognitive tasks (e.g., Stroop task) may have a “ceiling effect” that does not effectively reflect the effects of tDCS. Besides, laboratory tests lack high levels of ecological validity, which may complicate detection of the effects of tDCS in high-level athletes (Machado et al., 2021). Efficacy of stimulation may also depend on number of sessions. A previous study reported that a-tDCS (2 mA, 20 min) over the left DLPFC over ten consecutive days improved attention and memory in professional athletes (Borducchi et al., 2016). This implies that a single tDCS session may be insufficient to enhance cognitive performance in high-level athletes. Further research should explore the effects of tDCS on cognitive performance in high-level athletes using multi-session and sport-specific cognitive tasks.

Another brain region that plays an essential role in athletic performance regulation is the TC. Two studies included in this review investigated the effects of tDCS applied over the TC on endurance and cognitive function. Regarding endurance, one study found that 2-mA a-tDCS over the left TC for 20 min increased PPO in the MIT in cyclists. The TC is an important part of the central autonomic network, which is involved in higher-order control of autonomic cardiovascular functions (Dono et al., 2020). tDCS over the TC can furthermore increase neural excitability of the insular cortex (Montenegro et al., 2011). The insular cortex is a major contributor to awareness of the body and subjective feelings related to athletes’ perceptions of physical exertion during exercise and is responsible for cardiac autonomic control (Okano et al., 2015; Penna et al., 2021). It has been speculated that a-tDCS over the TC may increase parasympathetic modulation or decrease sympathetic modulation of the autonomic nervous system thereby improving endurance performance (Okano et al., 2015). Regarding cognitive function, one study reported that 2-mA a-tDCS over the middle TC for 20 min improved visuomotor and basketball decision-making skills in basketball players under mental fatigue (Fortes et al., 2022). Previous studies have also demonstrated an association of the TC with perception (e.g., visual search) in exercise (Brascamp et al., 2010; Qiu et al., 2019; Jedidi et al., 2021). Makris and Urgesi. (2015) showed that repetitive transcranial magnetic stimulation over the superior temporal sulcus decreased action anticipation in soccer players. The TC is a node in the action–observation network (Avenanti et al., 2013). tDCS over the TC may activate action-observation network and improve perceptual-cognitive skills in high-level athletes.

The presently reviewed studies contained 14 different electrode placement protocols with eight different reference electrode positions. Holgado et al. (2019) reported the effects of tDCS on exercise performance were not significantly moderated by type of outcome, electrode placement, muscles involved, number of sessions, or intensity and duration of the stimulation. Differences in electrode placement and stimulation protocols also contributed to mixed results. Anoushiravani et al. reported that tDCS over PMC have better effects in improving strength and sport-specific performance of gymnastic athletes in comparison with tDCS over CB (Anoushiravani et al., 2023). Some studies showed that tDCS over DLPFC and M1 yielded inconsistent results in the same swimming test (Valenzuela et al., 2019; Salehi et al., 2022). Athletic performance is influenced by a variety of abilities modulated by different brain regions, and few studies have examined the effects of stimulating different brain regions on identical athletic performance. Kamali et al. (2019) use a two channel a-tDCS, one anode electrode over M1 (Cz, C1 and C2) and one over TC (T3) for 13 min, and found improvements in one-repetition maximum loads in experienced bodybuilders. A recent study reported that corticospinal excitability was significantly higher following tDCS over M1 and DLPFC than M1 (Vaseghi et al., 2015). This implied that dual-site stimulation may have better effects. The effects of different stimulation protocols and dual-site stimulation on high-level athletes should be investigated in future studies.

5 Conclusion

A single session of 1.5–2.4-mA tDCS with a duration of 15–30 min improved strength, endurance, sport-specific performance, emotional states, and cognitive performance in national- or international-level athletes in 12 out of the 18 studies. Of these, six refer to the application of tDCS on the motor system (M1, PMC, CB), five on DLPFC and two on TC. Of all the variables examined in our review, the most sensitive to tDCS are strength (improvement in 67% of studies), endurance (improvement in 75% of studies), and emotional states (improvement in 75% of studies). It is interesting to note that the positive effects of tDCS on performance are significantly reduced in the case of sport-specific tasks (40% of studies) and cognitive performance (33% of studies). This suggests that tDCS is a promising tool to improve sportive performance but that it is more effective in no task specific aspects of athletic performance.

In conclusion, our work suggests that a single tDCS session can apply to competition and pre-competition training to improve athletic performance including both physical and psychological aspects of national- or international-level athletes. Given the relevance of tDCS as a tool to improve athletic performance, further studies focusing on various parameters (type of sports, brain regions, stimulation protocol, athlete level and test tasks) and neural mechanistic studies are needed to improve efficacy of tDCS interventions.

Funding Statement

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. The authors gratefully acknowledge funding support from Humanities and Social Sciences Research Funds of the Ministry of Education of China (22YJCZH136), the Fundamental Research Funds for the Central Universities (2022QN013) and the Research Foundation for Advanced Talents of Beijing Sport University.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.

Author contributions

YY: Investigation, Software, Visualization, Writing–original draft. XZ: Resources, Software, Writing–original draft. MN: Writing–review and editing. CV: Writing–review and editing. FQ: Conceptualization, Funding acquisition, Resources, Supervision, Writing–review and editing.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

  • Alix-Fages C., Romero-Arenas S., Castro-Alonso M., Colomer-Poveda D., Rio-Rodriguez D., Jerez-Martinez A., et al. (2019). Short-term effects of anodal transcranial direct current stimulation on endurance and maximal force production: a systematic review and meta-analysis. J. Clin. Med. 8 (4), 536. 10.3390/jcm8040536 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Al-Khelaifi F., Diboun I., Donati F., Botre F., Alsayrafi M., Georgakopoulos C., et al. (2018). A pilot study comparing the metabolic profiles of elite-level athletes from different sporting disciplines. Sports Medicine-Open 4, 2. 10.1186/s40798-017-0114-z [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Andrade D. C., Manzo O., Beltran A. R., Alvarez C., Del Rio R., Toledo C., et al. (2020). Kinematic and neuromuscular measures of intensity during plyometric jumps. J. Strength Cond. Res. 34 (12), 3395–3402. 10.1519/JSC.0000000000002143 [Abstract] [CrossRef] [Google Scholar]
  • Angius L., Hopker J., Mauger A. R. (2017). The ergogenic effects of transcranial direct current stimulation on exercise performance. Front. Physiology 8, 90. 10.3389/fphys.2017.00090 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Angius L., Santarnecchi E., Pascual-Leone A., Marcora S. M. (2019). Transcranial direct current stimulation over the left dorsolateral prefrontal cortex improves inhibitory control and endurance performance in healthy individuals. Neuroscience 419, 34–45. 10.1016/j.neuroscience.2019.08.052 [Abstract] [CrossRef] [Google Scholar]
  • Anoushiravani S., Alizadehgoradel J., Iranpour A., Yousefi Bilehsavar O., Pouresmali A., Nitsche M. A., et al. (2023). The impact of bilateral anodal transcranial direct current stimulation of the premotor and cerebellar cortices on physiological and performance parameters of gymnastic athletes: a randomized, cross-over, sham-controlled study. Sci. Rep. 13 (1), 10611. 10.1038/s41598-023-37843-1 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Avenanti A., Annella L., Candidi M., Urgesi C., Aglioti S. M. (2013). Compensatory plasticity in the action observation network: virtual lesions of STS enhance anticipatory simulation of seen actions. Cereb. Cortex 23 (3), 570–580. 10.1093/cercor/bhs040 [Abstract] [CrossRef] [Google Scholar]
  • Babiloni C., Marzano N., Infarinato F., Iacoboni M., Rizza G., Aschieri P., et al. (2010). Neural efficiency" of experts' brain during judgment of actions: a high-resolution EEG study in elite and amateur karate athletes. Behav. Brain Res. 207 (2), 466–475. 10.1016/j.bbr.2009.10.034 [Abstract] [CrossRef] [Google Scholar]
  • Behrangrad S., Zoghi M., Kidgell D., Mansouri F., Jaberzadeh S. (2022). The effects of concurrent bilateral anodal tDCS of primary motor cortex and cerebellum on corticospinal excitability: a randomized, double-blind sham-controlled study. Brain Struct. Funct. 227 (7), 2395–2408. 10.1007/s00429-022-02533-7 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Borducchi D. M., Gomes J. S., Akiba H., Cordeiro Q., Borducchi J. H., Valentin L. S., et al. (2016). Transcranial direct current stimulation effects on athletes' cognitive performance: an exploratory proof of concept trial. Front. Psychiatry 7, 183. 10.3389/fpsyt.2016.00183 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Brandt R., Bevilacqua G. G., Andrade A. (2017). Perceived sleep quality, mood states, and their relationship with performance among Brazilian elite athletes during a competitive period. J. Strength Cond. Res. 31 (4), 1033–1039. 10.1519/JSC.0000000000001551 [Abstract] [CrossRef] [Google Scholar]
  • Brascamp J. W., Kanai R., Walsh V., van Ee R. (2010). Human middle temporal cortex, perceptual bias, and perceptual memory for ambiguous three-dimensional motion. J. Neurosci. 30 (2), 760–766. 10.1523/jneurosci.4171-09.2010 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Callan D. E., Naito E. (2014). Neural processes distinguishing elite from expert and novice athletes. Cognitive Behav. Neurology 27 (4), 183–188. 10.1097/WNN.0000000000000043 [Abstract] [CrossRef] [Google Scholar]
  • Casanova F., Garganta J., Silva G., Alves A., Oliveira J., Williams A. M. (2013). Effects of prolonged intermittent exercise on perceptual-cognitive processes. Med. Sci. Sports Exerc 45 (8), 1610–1617. 10.1249/MSS.0b013e31828b2ce9 [Abstract] [CrossRef] [Google Scholar]
  • Celnik P. (2015). Understanding and modulating motor learning with cerebellar stimulation. Cerebellum 14 (2), 171–174. 10.1007/s12311-014-0607-y [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Chinzara T. T., Buckingham G., Harris D. J. (2022). Transcranial direct current stimulation and sporting performance: a systematic review and meta-analysis of transcranial direct current stimulation effects on physical endurance, muscular strength and visuomotor skills. Eur. J. Neurosci. 55 (2), 468–486. 10.1111/ejn.15540 [Abstract] [CrossRef] [Google Scholar]
  • Chiu C. N., Chen C. Y., Muggleton N. G. (2017). Sport, time pressure, and cognitive performance. Prog. Brain Res. 234, 85–99. 10.1016/bs.pbr.2017.06.007 [Abstract] [CrossRef] [Google Scholar]
  • Ciccone A. B., Deckert J. A., Schlabs C. R., Tilden M. J., Herda T. J., Gallagher P. M., et al. (2019). Transcranial direct current stimulation of the temporal lobe does not affect high-intensity work capacity. J. Strength Cond. Res. 33 (8), 2074–2086. 10.1519/JSC.0000000000002561 [Abstract] [CrossRef] [Google Scholar]
  • Colzato L. S., Nitsche M. A., Kibele A. (2016). Noninvasive brain stimulation and neural entrainment enhance athletic performance—a review. J. Cognitive Enhanc. 1 (1), 73–79. 10.1007/s41465-016-0003-2 [CrossRef] [Google Scholar]
  • Del Percio C., Infarinato F., Iacoboni M., Marzano N., Soricelli A., Aschieri P., et al. (2010). Movement-related desynchronization of alpha rhythms is lower in athletes than non-athletes: a high-resolution EEG study. Clin. Neurophysiol. 121 (4), 482–491. 10.1016/j.clinph.2009.12.004 [Abstract] [CrossRef] [Google Scholar]
  • Del Percio C., Rossini P. M., Marzano N., Iacoboni M., Infarinato F., Aschieri P., et al. (2008). Is there a "neural efficiency" in athletes? A high-resolution EEG study. Neuroimage 42 (4), 1544–1553. 10.1016/j.neuroimage.2008.05.061 [Abstract] [CrossRef] [Google Scholar]
  • Denis G., Zory R., Radel R. (2019). Testing the role of cognitive inhibition in physical endurance using high-definition transcranial direct current stimulation over the prefrontal cortex. Hum. Mov. Sci. 67, 102507. 10.1016/j.humov.2019.102507 [Abstract] [CrossRef] [Google Scholar]
  • Donati F., Sian V., Biasini G. M., de la Torre X., Folchitto F., Botre F. (2021). Serum levels of brain-derived neurotrophic factor and other neurotrophins in elite athletes: potential markers of the use of transcranial direct current stimulation in sport. Front. Sports Act. Living 3, 619573. 10.3389/fspor.2021.619573 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Dono F., Evangelista G., Frazzini V., Vollono C., Carrarini C., Russo M., et al. (2020). Interictal heart rate variability analysis reveals lateralization of cardiac autonomic control in temporal lobe epilepsy. Front. Neurol. 11, 842. 10.3389/fneur.2020.00842 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Dunst B., Benedek M., Jauk E., Bergner S., Koschutnig K., Sommer M., et al. (2014). Neural efficiency as a function of task demands. Intelligence 42 (100), 22–30. 10.1016/j.intell.2013.09.005 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Dutta A., Krishnan C., Kantak S. S., Ranganathan R., Nitsche M. A. (2015). Recurrence quantification analysis of surface electromyogram supports alterations in motor unit recruitment strategies by anodal transcranial direct current stimulation. Restor. Neurol. Neurosci. 33 (5), 663–669. 10.3233/RNN-140469 [Abstract] [CrossRef] [Google Scholar]
  • Edwards D. J., Cortes M., Wortman-Jutt S., Putrino D., Bikson M., Thickbroom G., et al. (2017). Transcranial direct current stimulation and sports performance. Front. Hum. Neurosci. 11, 243. 10.3389/fnhum.2017.00243 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Engle R. W. (2016). Working memory capacity as executive attention. Curr. Dir. Psychol. Sci. 11 (1), 19–23. 10.1111/1467-8721.00160 [CrossRef] [Google Scholar]
  • Ericsson Ka K. R., Tesch-Römer C., Tesch-Römer C. (1993). The role of deliberate practice in the acquisition of expert performance. Psychol. Rev. 100 (3), 363–406. 10.1037/0033-295X.100.3.363 [CrossRef] [Google Scholar]
  • Ermutlu N., Yucesir I., Eskikurt G., Temel T., Isoglu-Alkac U. (2015). Brain electrical activities of dancers and fast ball sports athletes are different. Cogn. Neurodyn 9 (2), 257–263. 10.1007/s11571-014-9320-2 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Fortes L. d.S., Faro H., de Lima-Junior D., Albuquerque M. R., Caputo Ferreira M. E. (2022a). Non-invasive brain stimulation over the orbital prefrontal cortex maintains endurance performance in mentally fatigued swimmers. Physiology Behav. 250, 113783. 10.1016/j.physbeh.2022.113783 [Abstract] [CrossRef] [Google Scholar]
  • Fortes L. S., Ferreira M. E. C., Faro H., Penna E. M., Almeida S. S. (2022b). Brain stimulation over the motion-sensitive midtemporal area reduces deleterious effects of mental fatigue on perceptual-cognitive skills in basketball players. J. Sport and Exerc. Psychol. 44 (4), 272–285. 10.1123/jsep.2021-0281 [Abstract] [CrossRef] [Google Scholar]
  • Frazer A., Williams J., Spittles M., Rantalainen T., Kidgell D. (2016). Anodal transcranial direct current stimulation of the motor cortex increases cortical voluntary activation and neural plasticity. Muscle Nerve 54 (5), 903–913. 10.1002/mus.25143 [Abstract] [CrossRef] [Google Scholar]
  • Fregni F., Boggio P. S., Nitsche M. A., Rigonatti S. P., Pascual-Leone A. (2006). Cognitive effects of repeated sessions of transcranial direct current stimulation in patients with depression. Depress Anxiety 23 (8), 482–484. 10.1002/da.20201 [Abstract] [CrossRef] [Google Scholar]
  • Galea J. M., Jayaram G., Ajagbe L., Celnik P. (2009). Modulation of cerebellar excitability by polarity-specific noninvasive direct current stimulation. J. Neurosci. 29 (28), 9115–9122. 10.1523/JNEUROSCI.2184-09.2009 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Gallo G., Geda E., Codella R., Faelli E., Panasci M., Ranieri L. E., et al. (2022). Effects of bilateral dorsolateral prefrontal cortex high-definition transcranial direct-current stimulation on physiological and performance responses at severe-intensity exercise domain in elite road cyclists. Int. J. Sports Physiol. Perform. 17 (7), 1085–1093. 10.1123/ijspp.2022-0019 [Abstract] [CrossRef] [Google Scholar]
  • Gold J., Ciorciari J. (2021). Impacts of transcranial direct current stimulation on the action observation network and sports anticipation task. J. Sport and Exerc. Psychol. 43 (4), 310–322. 10.1123/jsep.2020-0109 [Abstract] [CrossRef] [Google Scholar]
  • Guo Z., Li A., Yu L. (2017). Neural efficiency" of athletes' brain during visuo-spatial task: an fMRI study on table tennis players. Front. Behav. Neurosci. 11, 72. 10.3389/fnbeh.2017.00072 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Habay J., Van Cutsem J., Verschueren J., De Bock S., Proost M., De Wachter J., et al. (2021). Mental fatigue and sport-specific psychomotor performance: a systematic review. Sports Med. 51 (7), 1527–1548. 10.1007/s40279-021-01429-6 [Abstract] [CrossRef] [Google Scholar]
  • Hagan J. E., Jr., Pollmann D., Schack T. (2017). Elite athletes' in-event competitive anxiety responses and psychological skills usage under differing conditions. Front. Psychol. 8, 2280. 10.3389/fpsyg.2017.02280 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Hazime F. A., Cunha R. A. d., Soliaman R. R., Romancini A. C. B., Pochini A. d.C., Ejnisman B., et al. (2017). ANODAL TRANSCRANIAL DIRECT CURRENT STIMULATION (TDCS) INCREASES ISOMETRIC STRENGTH OF SHOULDER ROTATORS MUSCLES IN HANDBALL PLAYERS. Int. J. Sports Phys. Ther. 12 (3), 402–407. [Europe PMC free article] [Abstract] [Google Scholar]
  • Holgado D., Vadillo M. A., Sanabria D. (2019). The effects of transcranial direct current stimulation on objective and subjective indexes of exercise performance: a systematic review and meta-analysis. Brain Stimul. 12 (2), 242–250. 10.1016/j.brs.2018.12.002 [Abstract] [CrossRef] [Google Scholar]
  • Hou J., Nitsche M. A., Yi L., Kong Z., Qi F. (2022). Effects of transcranial direct current stimulation over the primary motor cortex in improving postural stability in healthy young adults. Biol. (Basel) 11 (9), 1370. 10.3390/biology11091370 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Irwin C., Desbrow B., Ellis A., O'Keeffe B., Grant G., Leveritt M. (2011). Caffeine withdrawal and high-intensity endurance cycling performance. J. Sports Sci. 29 (5), 509–515. 10.1080/02640414.2010.541480 [Abstract] [CrossRef] [Google Scholar]
  • Jacobs J. V., Horak F. B. (2007). Cortical control of postural responses. J. Neural Transm. (Vienna) 114 (10), 1339–1348. 10.1007/s00702-007-0657-0 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Jamil A., Batsikadze G., Kuo H. I., Labruna L., Hasan A., Paulus W., et al. (2017). Systematic evaluation of the impact of stimulation intensity on neuroplastic after-effects induced by transcranial direct current stimulation. J. physiology 595 (4), 1273–1288. 10.1113/JP272738 [Abstract] [CrossRef] [Google Scholar]
  • Jedidi Z., Manard M., Balteau E., Degueldre C., Luxen A., Phillips C., et al. (2021). Incidental verbal semantic processing recruits the fronto-temporal semantic control network. Cereb. Cortex 31 (12), 5449–5459. 10.1093/cercor/bhab169 [Abstract] [CrossRef] [Google Scholar]
  • Kamali A. M., Saadi Z. K., Yahyavi S. S., Zarifkar A., Aligholi H., Nami M. (2019). Transcranial direct current stimulation to enhance athletic performance outcome in experienced bodybuilders. PLoS One 14 (8), e0220363. 10.1371/journal.pone.0220363 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Kaminski E., Steele C. J., Hoff M., Gundlach C., Rjosk V., Sehm B., et al. (2016). Transcranial direct current stimulation (tDCS) over primary motor cortex leg area promotes dynamic balance task performance. Clin. Neurophysiol. 127 (6), 2455–2462. 10.1016/j.clinph.2016.03.018 [Abstract] [CrossRef] [Google Scholar]
  • Kantak S. S., Stinear J. W., Buch E. R., Cohen L. G. (2012). Rewiring the brain: potential role of the premotor cortex in motor control, learning, and recovery of function following brain injury. Neurorehabil Neural Repair 26 (3), 282–292. 10.1177/1545968311420845 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Keeser D., Meindl T., Bor J., Palm U., Pogarell O., Mulert C., et al. (2011). Prefrontal transcranial direct current stimulation changes connectivity of resting-state networks during fMRI. J. Neurosci. 31 (43), 15284–15293. 10.1523/JNEUROSCI.0542-11.2011 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Kenville R., Maudrich T., Maudrich D., Villringer A., Ragert P. (2020). Cerebellar transcranial direct current stimulation improves maximum isometric force production during isometric barbell squats. Brain Sci. 10 (4), 235. 10.3390/brainsci10040235 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Khedr E. M., Omran E. A. H., Ismail N. M., El-Hammady D. H., Goma S. H., Kotb H., et al. (2017). Effects of transcranial direct current stimulation on pain, mood and serum endorphin level in the treatment of fibromyalgia: a double blinded, randomized clinical trial. Brain Stimul. 10 (5), 893–901. 10.1016/j.brs.2017.06.006 [Abstract] [CrossRef] [Google Scholar]
  • Krishnan C., Ranganathan R., Kantak S. S., Dhaher Y. Y., Rymer W. Z. (2014). Anodal transcranial direct current stimulation alters elbow flexor muscle recruitment strategies. Brain Stimul. 7 (3), 443–450. 10.1016/j.brs.2014.01.057 [Abstract] [CrossRef] [Google Scholar]
  • Lang N., Siebner H. R., Ward N. S., Lee L., Nitsche M. A., Paulus W., et al. (2005). How does transcranial DC stimulation of the primary motor cortex alter regional neuronal activity in the human brain? Eur. J. Neurosci. 22 (2), 495–504. 10.1111/j.1460-9568.2005.04233.x [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Lattari E., Andrade M. L., Filho A. S., Moura A. M., Neto G. M., Silva J. G., et al. (2016). Can transcranial direct current stimulation improve the resistance strength and decrease the rating perceived scale in recreational weight-training experience? J. Strength Cond. Res. 30 (12), 3381–3387. 10.1519/jsc.0000000000001457 [Abstract] [CrossRef] [Google Scholar]
  • Liang Z., Zhou J., Jiao F., Gin T., Wang X., Liu Y., et al. (2022). Effect of transcranial direct current stimulation on endurance performance in elite female rowers: a pilot, single-blinded study. Brain Sci. 12 (5), 541. 10.3390/brainsci12050541 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Liberati A., Altman D. G., Tetzlaff J., Mulrow C., Gotzsche P. C., Ioannidis J. P., et al. (2009). The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. J. Clin. Epidemiol. 62 (10), e1–e34. 10.1016/j.jclinepi.2009.06.006 [Abstract] [CrossRef] [Google Scholar]
  • Liebetanz D., Nitsche M. A., Tergau F., Paulus W. (2002). Pharmacological approach to the mechanisms of transcranial DC-stimulation-induced after-effects of human motor cortex excitability. Brain 125, 2238–2247. 10.1093/brain/awf238 [Abstract] [CrossRef] [Google Scholar]
  • Ligeza T. S., Nowak I., Maciejczyk M., Szygula Z., Wyczesany M. (2021). Acute aerobic exercise enhances cortical connectivity between structures involved in shaping mood and improves self-reported mood: an EEG effective-connectivity study in young male adults. Int. J. Psychophysiol. 162, 22–33. 10.1016/j.ijpsycho.2021.01.016 [Abstract] [CrossRef] [Google Scholar]
  • Lu P. P., Hanson N. J., Wen L., Guo F., Tian X. Y. (2021). Transcranial direct current stimulation enhances muscle strength of non-dominant knee in healthy young males. Front. Physiology 12, 788719. 10.3389/fphys.2021.788719 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Machado D. G. D., Bikson M., Datta A., Caparelli-Daquer E., Unal G., Baptista A. F., et al. (2021). Acute effect of high-definition and conventional tDCS on exercise performance and psychophysiological responses in endurance athletes: a randomized controlled trial. Sci. Rep. 11 (1), 15. 10.1038/s41598-021-92670-6 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Machado D. G. D. S., Unal G., Andrade S. M., Moreira A., Altimari L. R., Brunoni A. R., et al. (2019a). Effect of transcranial direct current stimulation on exercise performance: a systematic review and meta-analysis. Brain Stimul. 12 (3), 593–605. 10.1016/j.brs.2018.12.227 [Abstract] [CrossRef] [Google Scholar]
  • Machado S., Jansen P., Almeida V., Veldema J. (2019b). Is tDCS an adjunct ergogenic resource for improving muscular strength and endurance performance? A systematic review. Front. Psychol. 10, 1127. 10.3389/fpsyg.2019.01127 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Maeoka H., Matsuo A., Hiyamizu M., Morioka S., Ando H. (2012). Influence of transcranial direct current stimulation of the dorsolateral prefrontal cortex on pain related emotions: a study using electroencephalographic power spectrum analysis. Neurosci. Lett. 512 (1), 12–16. 10.1016/j.neulet.2012.01.037 [Abstract] [CrossRef] [Google Scholar]
  • Maezawa H., Vicario C. M., Kuo M.-F., Hirata M., Mima T., Nitsche M. A. (2020). Effects of bilateral anodal transcranial direct current stimulation over the tongue primary motor cortex on cortical excitability of the tongue and tongue motor functions. Brain Stimul. 13 (1), 270–272. 10.1016/j.brs.2019.10.005 [Abstract] [CrossRef] [Google Scholar]
  • Makris S., Urgesi C. (2015). Neural underpinnings of superior action prediction abilities in soccer players. Soc. Cognitive Affect. Neurosci. 10 (3), 342–351. 10.1093/scan/nsu052 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Marinus N., Van Hoornweder S., Aarts M., Vanbilsen J., Hansen D., Meesen R. (2022). The influence of a single transcranial direct current stimulation session on physical fitness in healthy subjects: a systematic review. Exp. Brain Res. 241 (1), 31–47. 10.1007/s00221-022-06494-5 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Maudrich T., Ragert P., Perrey S., Kenville R. (2022). Single-session anodal transcranial direct current stimulation to enhance sport-specific performance in athletes: a systematic review and meta-analysis. Brain Stimul. 15 (6), 1517–1529. 10.1016/j.brs.2022.11.007 [Abstract] [CrossRef] [Google Scholar]
  • McKay A. K. A., Stellingwerff T., Smith E. S., Martin D. T., Mujika I., Goosey-Tolfrey V. L., et al. (2022). Defining training and performance caliber: a participant classification framework. Int. J. Sports Physiol. Perform. 17 (2), 317–331. 10.1123/ijspp.2021-0451 [Abstract] [CrossRef] [Google Scholar]
  • Mehrsafar A. H., Rosa M. A. S., Zadeh A. M., Gazerani P. (2020). A feasibility study of application and potential effects of a single session transcranial direct current stimulation (tDCS) on competitive anxiety, mood state, salivary levels of cortisol and alpha amylase in elite athletes under a real-world competition. Physiol. Behav. 227, 113173. 10.1016/j.physbeh.2020.113173 [Abstract] [CrossRef] [Google Scholar]
  • Mesquita P. H. C., Franchini E., Romano-Silva M. A., Lage G. M., Albuquerque M. R. (2020). Transcranial direct current stimulation: No effect on aerobic performance, heart rate, or rating of perceived exertion in a progressive taekwondo-specific test. Int. J. Sports Physiology Perform. 15 (7), 958–963. 10.1123/ijspp.2019-0410 [Abstract] [CrossRef] [Google Scholar]
  • Mesquita P. H. C., Lage G. M., Franchini E., Romano-Silva M. A., Albuquerque M. R. (2019a). Bi-hemispheric anodal transcranial direct current stimulation worsens taekwondo-related performance. Hum. Mov. Sci. 66, 578–586. 10.1016/j.humov.2019.06.003 [Abstract] [CrossRef] [Google Scholar]
  • Mesquita P. H. C., Lage G. M., Franchini E., Romano-Silva M. A., Albuquerque M. R. (2019b). Bi-hemispheric anodal transcranial direct current stimulation worsens taekwondo-related performance. Hum. Mov. Sci. 66, 578–586. 10.1016/j.humov.2019.06.003 [Abstract] [CrossRef] [Google Scholar]
  • Miller E. K., Cohen J. D. (2001). An integrative theory of prefrontal cortex function. Annu. Rev. Neurosci. 24, 167–202. 10.1146/annurev.neuro.24.1.167 [Abstract] [CrossRef] [Google Scholar]
  • Monda V., Valenzano A., Moscatelli F., Salerno M., Sessa F., Triggiani A. I., et al. (2017). Primary motor cortex excitability in karate athletes: a transcranial magnetic stimulation study. Front. Physiol. 8, 695. 10.3389/fphys.2017.00695 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Montenegro R. A., Farinatti Pde T., Fontes E. B., Soares P. P., Cunha F. A., Gurgel J. L., et al. (2011). Transcranial direct current stimulation influences the cardiac autonomic nervous control. Neurosci. Lett. 497 (1), 32–36. 10.1016/j.neulet.2011.04.019 [Abstract] [CrossRef] [Google Scholar]
  • Moreira A., Machado D., Moscaleski L., Bikson M., Unal G., Bradley P. S., et al. (2021). Effect of tDCS on well-being and autonomic function in professional male players after official soccer matches. Physiol. Behav. 233, 113351. 10.1016/j.physbeh.2021.113351 [Abstract] [CrossRef] [Google Scholar]
  • Moreira A., Moscaleski L., Machado D. G. D., Bikson M., Unal G., Bradley P. S., et al. (2022). Transcranial direct current stimulation during a prolonged cognitive task: the effect on cognitive and shooting performances in professional female basketball players. Ergonomics 66, 492–505. 10.1080/00140139.2022.2096262 [Abstract] [CrossRef] [Google Scholar]
  • Morya E., Monte-Silva K., Bikson M., Esmaeilpour Z., Biazoli C. E., Fonseca A., et al. (2019). Beyond the target area: an integrative view of tDCS-induced motor cortex modulation in patients and athletes. J. Neuroengineering Rehabilitation 16 (1), 141. 10.1186/s12984-019-0581-1 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Nakamoto H., Mori S. (2008). Effects of stimulus-response compatibility in mediating expert performance in baseball players. Brain Res. 1189, 179–188. 10.1016/j.brainres.2007.10.096 [Abstract] [CrossRef] [Google Scholar]
  • Nakata H., Yoshie M., Miura A., Kudo K. (2010). Characteristics of the athletes' brain: evidence from neurophysiology and neuroimaging. Brain Res. Rev. 62 (2), 197–211. 10.1016/j.brainresrev.2009.11.006 [Abstract] [CrossRef] [Google Scholar]
  • Nitsche M. A., Fricke K., Henschke U., Schlitterlau A., Liebetanz D., Lang N., et al. (2003a). Pharmacological modulation of cortical excitability shifts induced by transcranial direct current stimulation in humans. J. Physiol. 553 (Pt 1), 293–301. 10.1113/jphysiol.2003.049916 [Abstract] [CrossRef] [Google Scholar]
  • Nitsche M. A., Paulus W. (2000). Excitability changes induced in the human motor cortex by weak transcranial direct current stimulation. J. Physiol. 527 (Pt 3), 633–639. 10.1111/j.1469-7793.2000.t01-1-00633.x [Abstract] [CrossRef] [Google Scholar]
  • Nitsche M. A., Paulus W. (2001). Sustained excitability elevations induced by transcranial DC motor cortex stimulation in humans. Neurology 57 (10), 1899–1901. 10.1212/wnl.57.10.1899 [Abstract] [CrossRef] [Google Scholar]
  • Nitsche M. A., Schauenburg A., Lang N., Liebetanz D., Exner C., Paulus W., et al. (2003b). Facilitation of implicit motor learning by weak transcranial direct current stimulation of the primary motor cortex in the human. J. Cogn. Neurosci. 15 (4), 619–626. 10.1162/089892903321662994 [Abstract] [CrossRef] [Google Scholar]
  • Noakes T. D. (2011). Time to move beyond a brainless exercise physiology: the evidence for complex regulation of human exercise performance. Appl. Physiology Nutr. Metabolism 36 (1), 23–35. 10.1139/h10-082 [Abstract] [CrossRef] [Google Scholar]
  • Okano A. H., Fontes E. B., Montenegro R. A., Veras Farinatti P. d.T., Cyrino E. S., Li L. M., et al. (2015). Brain stimulation modulates the autonomic nervous system, rating of perceived exertion and performance during maximal exercise. Br. J. Sports Med. 49 (18), 1213–1218. 10.1136/bjsports-2012-091658 [Abstract] [CrossRef] [Google Scholar]
  • Park S. B., Han D. H., Hong J., Lee J. W. (2022). Transcranial direct current stimulation of motor cortex enhances spike performances of professional female volleyball players. J. Mot. Behav. 55, 18–30. 10.1080/00222895.2022.2090489 [Abstract] [CrossRef] [Google Scholar]
  • Park S. Y., Reinl M., Schott N. (2021). Effects of acute exercise at different intensities on fine motor-cognitive dual-task performance while walking: a functional near-infrared spectroscopy study. Eur. J. Neurosci. 54 (12), 8225–8248. 10.1111/ejn.15241 [Abstract] [CrossRef] [Google Scholar]
  • Patel R., Ashcroft J., Patel A., Ashrafian H., Woods A. J., Singh H., et al. (2019). The impact of transcranial direct current stimulation on upper-limb motor performance in healthy adults: a systematic review and meta-analysis. Front. Neurosci. 13, 1213. 10.3389/fnins.2019.01213 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Penna E. M., Filho E., Campos B. T., Ferreira R. M., Parma J. O., Lage G. M., et al. (2021). No effects of mental fatigue and cerebral stimulation on physical performance of master swimmers. Front. Psychol. 12, 656499. 10.3389/fpsyg.2021.656499 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Piretti L., Pappaianni E., Gobbo S., Rumiati R. I., Job R., Grecucci A. (2022). Dissociating the role of dACC and dlPFC for emotion appraisal and mood regulation using cathodal tDCS. Cogn. Affect Behav. Neurosci. 22 (2), 304–315. 10.3758/s13415-021-00952-3 [Abstract] [CrossRef] [Google Scholar]
  • Polania R., Nitsche M. A., Ruff C. C. (2018). Studying and modifying brain function with non-invasive brain stimulation. Nat. Neurosci. 21 (2), 174–187. 10.1038/s41593-017-0054-4 [Abstract] [CrossRef] [Google Scholar]
  • Polania R., Paulus W., Nitsche M. A. (2012). Modulating cortico-striatal and thalamo-cortical functional connectivity with transcranial direct current stimulation. Hum. Brain Mapp. 33 (10), 2499–2508. 10.1002/hbm.21380 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Pollastri L., Gallo G., Zucca M., Filipas L., la Torre A., Riba U., et al. (2021). Bilateral dorsolateral prefrontal cortex high-definition transcranial direct-current stimulation improves time-trial performance in elite cyclists. Int. J. Sports Physiology Perform. 16 (2), 224–231. 10.1123/IJSPP.2019-0910 [Abstract] [CrossRef] [Google Scholar]
  • Post M., Steens A., Renken R., Maurits N. M., Zijdewind I. (2009). Voluntary activation and cortical activity during a sustained maximal contraction: an fMRI study. Hum. Brain Mapp. 30 (3), 1014–1027. 10.1002/hbm.20562 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Qiu F. H., Pi Y. L., Liu K., Zhu H., Li X. P., Zhang J., et al. (2019). Neural efficiency in basketball players is associated with bidirectional reductions in cortical activation and deactivation during multiple-object tracking task performance. Biol. Psychol. 144, 28–36. 10.1016/j.biopsycho.2019.03.008 [Abstract] [CrossRef] [Google Scholar]
  • Salehi E. N., Fard S. J., Jaberzadeh S., Zoghi M. (2022). Transcranial direct current stimulation reduces the negative impact of mental fatigue on swimming performance. J. Mot. Behav. 54 (3), 327–336. 10.1080/00222895.2021.1962238 [Abstract] [CrossRef] [Google Scholar]
  • Sami S., Miall R. C. (2013). Graph network analysis of immediate motor-learning induced changes in resting state BOLD. Front. Hum. Neurosci. 7, 166. 10.3389/fnhum.2013.00166 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Shyamali Kaushalya F., Romero-Arenas S., Garcia-Ramos A., Colomer-Poveda D., Marquez G. (2021). Acute effects of transcranial direct current stimulation on cycling and running performance. A systematic review and meta-analysis. Eur. J. Sport Sci. 22, 113–125. 10.1080/17461391.2020.1856933 [Abstract] [CrossRef] [Google Scholar]
  • Smith M. R., Zeuwts L., Lenoir M., Hens N., De Jong L. M., Coutts A. J. (2016). Mental fatigue impairs soccer-specific decision-making skill. J. Sports Sci. 34 (14), 1297–1304. 10.1080/02640414.2016.1156241 [Abstract] [CrossRef] [Google Scholar]
  • Stagg C. J., Lin R. L., Mezue M., Segerdahl A., Kong Y., Xie J., et al. (2013). Widespread modulation of cerebral perfusion induced during and after transcranial direct current stimulation applied to the left dorsolateral prefrontal cortex. J. Neurosci. 33 (28), 11425–11431. 10.1523/JNEUROSCI.3887-12.2013 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Stagg C. J., Nitsche M. A. (2011). Physiological basis of transcranial direct current stimulation. Neuroscientist 17 (1), 37–53. 10.1177/1073858410386614 [Abstract] [CrossRef] [Google Scholar]
  • To W. T., De Ridder D., Hart J., Jr., Vanneste S. (2018). Changing brain networks through non-invasive neuromodulation. Front. Hum. Neurosci. 12, 128. 10.3389/fnhum.2018.00128 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Unger R. H., Lowe M. J., Beall E. B., Bethoux F., Jones S. E., Machado A. G., et al. (2023). Stimulation of the premotor cortex enhances interhemispheric functional connectivity in association with upper limb motor recovery in moderate-to-severe chronic stroke. Brain Connect. 13, 453–463. 10.1089/brain.2022.0064 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Vahdat S., Darainy M., Ostry D. J. (2014). Structure of plasticity in human sensory and motor networks due to perceptual learning. J. Neurosci. 34 (7), 2451–2463. 10.1523/jneurosci.4291-13.2014 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Valenzuela P. L., Amo C., Sanchez-Martinez G., Torrontegi E., Vazquez-Carrion J., Montalvo Z., et al. (2019). Enhancement of mood but not performance in elite athletes with transcranial direct-current stimulation. Int. J. Sports Physiol. Perform. 14 (3), 310–316. 10.1123/ijspp.2018-0473 [Abstract] [CrossRef] [Google Scholar]
  • van den Heuvel M. P., Sporns O. (2013). Network hubs in the human brain. Trends Cogn. Sci. 17 (12), 683–696. 10.1016/j.tics.2013.09.012 [Abstract] [CrossRef] [Google Scholar]
  • Vargas V. Z., Baptista A. F., Pereira G. O. C., Pochini A. C., Ejnisman B., Santos M. B., et al. (2018). Modulation of isometric quadriceps strength in soccer players with transcrinal direct current stimulation: a crossover study. J. Strength Cond. Res. 32 (5), 1336–1341. 10.1519/jsc.0000000000001985 [Abstract] [CrossRef] [Google Scholar]
  • Vaseghi B., Zoghi M., Jaberzadeh S. (2015). The effects of anodal-tDCS on corticospinal excitability enhancement and its after-effects: conventional vs. unihemispheric concurrent dual-site stimulation. Front. Hum. Neurosci. 9, 533. 10.3389/fnhum.2015.00533 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Veldema J., Engelhardt A., Jansen P. (2021). Does anodal tDCS improve basketball performance? A randomized controlled trial. Eur. J. Sport Sci. 22, 126–135. 10.1080/17461391.2020.1862306 [Abstract] [CrossRef] [Google Scholar]
  • Vieira L. A. F., Lattari E., de Jesus Abreu M. A., Rodrigues G. M., Viana B., Machado S., et al. (2020). Transcranial direct current stimulation (tDCS) improves back-squat performance in intermediate resistance-training men. Res. Q. Exerc Sport 93, 210–218. 10.1080/02701367.2020.1815638 [Abstract] [CrossRef] [Google Scholar]
  • Wagner H., Pfusterschmied J., Tilp M., Landlinger J., von Duvillard S. P., Müller E. (2014). Upper-body kinematics in team-handball throw, tennis serve, and volleyball spike. Scand. J. Med. Sci. Sports 24 (2), 345–354. 10.1111/j.1600-0838.2012.01503.x [Abstract] [CrossRef] [Google Scholar]
  • Wiegand A., Sommer A., Nieratschker V., Plewnia C. (2019). Improvement of cognitive control and stabilization of affect by prefrontal transcranial direct current stimulation (tDCS). Sci. Rep. 9 (1), 6797. 10.1038/s41598-019-43234-2 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Wood G., Vine S. J., Wilson M. R. (2016). Working memory capacity, controlled attention and aiming performance under pressure. Psychol. Res. 80 (4), 510–517. 10.1007/s00426-015-0673-x [Abstract] [CrossRef] [Google Scholar]
  • Wright M. J., Bishop D. T., Jackson R. C., Abernethy B. (2010). Functional MRI reveals expert-novice differences during sport-related anticipation. Neuroreport 21 (2), 94–98. 10.1097/WNR.0b013e328333dff2 [Abstract] [CrossRef] [Google Scholar]
  • Xu H., Wang P., Ye Z., Di X., Xu G., Mo L., et al. (2016). The role of medial frontal cortex in action anticipation in professional badminton players. Front. Psychol. 7, 1817. 10.3389/fpsyg.2016.01817 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Yang D., Shin Y. I., Hong K. S. (2021). Systemic review on transcranial electrical stimulation parameters and EEG/fNIRS features for brain diseases. Front. Neurosci. 15, 629323. 10.3389/fnins.2021.629323 [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]
  • Yosephi M. H., Ehsani F., Zoghi M., Jaberzadeh S. (2018). Multi-session anodal tDCS enhances the effects of postural training on balance and postural stability in older adults with high fall risk: primary motor cortex versus cerebellar stimulation. Brain Stimul. 11 (6), 1239–1250. 10.1016/j.brs.2018.07.044 [Abstract] [CrossRef] [Google Scholar]
  • Zandi L., Rad L. S. (2013). A comparison of the mood state profiles of winning and losing female athletes. Eur. J. Exp. Biol. 3 (1), 424–428. [Google Scholar]
  • Zhu F. F., Yeung A. Y., Poolton J. M., Lee T. M., Leung G. K., Masters R. S. (2015). Cathodal transcranial direct current stimulation over left dorsolateral prefrontal cortex area promotes implicit motor learning in a golf putting task. Brain Stimul. 8 (4), 784–786. 10.1016/j.brs.2015.02.005 [Abstract] [CrossRef] [Google Scholar]

Articles from Frontiers in Physiology are provided here courtesy of Frontiers Media SA

Citations & impact 


Impact metrics

Jump to Citations

Article citations

Similar Articles 


To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation.