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NCT Number: NCT07831512

Effect of Transcranial Direct Current Stimulation on Flywheel Resistance Training

Transcranial direct current stimulation (tDCS) has been investigated as an ergogenic strategy; however, its acute effects on muscle power-especially when combined with flywheel resistance training (FRT)-have not yet been explored. The aim of this study is to investigate the acute effects of anodal, cathodal, and sham tDCS on muscle power and neuromuscular variables during flywheel squat exercise. This is a randomized, double-blind, placebo-controlled, crossover clinical trial; 22 physically active men aged 18 to 35 years with strength training experience will be recruited. Volunteers will complete a minimum of three familiarization sessions and three experimental sessions, during which they will undergo anodal, cathodal, or sham tDCS conditions (2 mA, 20 min) in random order, with a minimum 48-hour interval between sessions. Following each stimulation, they will perform four sets of 1+8 repetitions of the flywheel squat. Concentric and eccentric power, the eccentric/concentric ratio, electromyographic activation (RMS, median and peak frequency), and subjective ratings of perceived exertion and discomfort will be analyzed. A repeated-measures ANOVA (3 conditions × 4 sets × 3 periods) will be performed, with Bonferroni post-hoc testing and a significance level of p < 0.05 for all analyses.

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Key information

Age range

18 year–40 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male sex,
  • Age 18-40 years,
  • Performance of barbell squats with a load > 1.5 times body mass (BM),
  • No current use or use within the last 6 months of ergogenic aids,
  • No history of muscle and/or ligament injuries in the last six months,
  • Absence of skin conditions that could be affected by tDCS,
  • Absence of unstable medical conditions,
  • No metallic objects near the electrodes.

Exclusion criteria

  • Failure to complete any stage of the study,
  • Injury during the intervention,
  • Reports of unbearable discomfort.

Treatment and study plan

tDCS-a

Other

For anodic stimulation (tDCS-a), the anode (positive electrode) will be positioned over the left M1 (point C3 of the international 10-20 system) (Figure 2), while the cathode will be placed over the contralateral deltoid.

tDCS-c

Other

In cathodal stimulation (tDCS-c), the polarity is reversed: the cathode is positioned at C3 and the anode on the contralateral deltoid.

Sham - tDCS

Other

For the placebo condition (sham-tDCS), the electrodes will be placed in the same position as in the anodal condition, but the stimulator will be turned off after 30 seconds. This procedure, considered ineffective for inducing cortical changes, allows subjects to feel only the initial tingling sensation, ensuring participant blinding regarding the type of intervention received.

Primary outcomes

  1. Muscular power

    Time frame: 2 weeks, with 3 visits to the laboratory

    Measured by a rotary encoder

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Sponsors and collaborators

Lead sponsor

Federal University of Vicosa

Other

Collaborators

  • Conselho Nacional de Desenvolvimento Científico e Tecnológico

Registry information

Official study title

Acute Effect of Transcranial Direct Current Stimulation on Power During Flywheel Squatting: a Randomized, Placebo-controlled, Crossover Clinical Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Sep 21, 2026
Registry last updated
Sep 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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