このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Acute Effects of Accelerated Transcranial Direct Current Stimulation on Leg Muscle Strength in Physically Inactive College Students (ACC-tDCS)

2026年10月29日 更新者:Beijing Sport University

Effects of Accelerated Transcranial Direct Current Stimulation on Lower Limb Muscle Strength in Adults: a Randomized, Single-Blind, Sham-Controlled Trial in Physically Inactive College Students

The goal of this clinical trial is to learn whether accelerated transcranial direct current stimulation (tDCS), in which two sessions of stimulation are delivered within a single day, can immediately improve leg muscle strength in physically inactive college students. tDCS is a non-invasive technique that applies a weak, constant electrical current through electrodes on the scalp to change the excitability of the brain area under the electrode. In this study, stimulation targets the leg area of the primary motor cortex.

The main questions it aims to answer are:

  • Does a single application of accelerated tDCS or single-session tDCS improve maximal strength, explosive strength and muscular endurance of the knee muscles more than sham stimulation?
  • Does dividing stimulation into two 10-minute sessions separated by 3 or 20 minutes produce larger immediate effects than one 10-minute or one 20-minute session?

Researchers will compare five groups: two accelerated tDCS groups (two 10-minute sessions separated by 3 or 20 minutes), two single-session tDCS groups (one 10-minute or one 20-minute session) and a sham stimulation group.

Participants will:

  • Attend one laboratory visit
  • Complete isokinetic strength tests of the knee flexors and extensors of both legs before stimulation
  • Receive the assigned stimulation protocol while sitting at rest
  • Repeat the same strength tests immediately after stimulation and report any sensations or discomfort related to stimulation

調査の概要

詳細な説明

Background: Muscle strength comprises maximal strength, explosive strength and muscular endurance. Anodal tDCS over the primary motor cortex (M1) can increase motor cortical excitability, and several studies have reported improvements in muscle strength after single sessions. Neurophysiological studies show that a second session of anodal tDCS delivered within the after-effect period of the first (for example after 3 or 20 minutes) prolongs the increase in cortical excitability, whereas longer intervals do not. Protocols that deliver two or more sessions within one day are termed accelerated tDCS. Accelerated protocols have been applied in cognitive and clinical research, but their effects on muscle strength have not been examined.

Objective: To compare the acute effects of accelerated and single-session anodal tDCS over M1 on maximal strength, explosive strength and muscular endurance of the lower limbs in physically inactive college students.

Design: Single-center, randomized, single-blind, sham-controlled, five-arm parallel-group trial conducted at Beijing Sport University, Beijing, China. The protocol was approved by the Sports Science Experiment Ethics Committee of Beijing Sport University (No. 2025391H), and all participants provide written informed consent.

Participants: Seventy-five physically inactive college students aged 18 to 25 years (15 per group). Physical inactivity is defined as fewer than three sessions per week of moderate-intensity exercise lasting at least 30 minutes during the previous 3 months.

Randomization and blinding: Randomization is stratified by sex. A researcher not involved in testing or stimulation generates separate random number sequences for men and women in SPSS 27.0 and allocates participants of each sex to the five groups. Participants are blinded to the stimulation condition, and the researchers who collect and analyze the data are not involved in group allocation.

Interventions: tDCS is delivered with a dual-channel stimulator (TCS-E2, Shenzhen Yingchi Technology Co., Ltd., Shenzhen, China) through saline-soaked sponge electrodes (35 cm2, 5 x 7 cm). The anode is placed over Cz (leg area of M1), located according to the international 10-20 system and confirmed with a positioning cap, and the cathode over Fpz. Active stimulation is delivered at 1 mA. The five groups are: (1) two 10-minute sessions separated by 3 minutes; (2) two 10-minute sessions separated by 20 minutes; (3) one 10-minute session; (4) one 20-minute session; (5) sham stimulation, in which current is ramped up over 15 seconds and down over 15 seconds and the electrodes remain in place for 10 minutes (n = 8) or 20 minutes (n = 7). Participants remain seated at rest during stimulation.

Procedures: At a single laboratory visit, participants complete a 3-minute warm-up on the isokinetic dynamometer and the baseline test (T0). After a 10-minute rest, the assigned stimulation protocol is administered, and the same tests are repeated immediately after stimulation (T1), followed by a cool-down. Tests are performed on a Biodex System 4 Pro dynamometer in reciprocal concentric mode for the knee flexors and extensors of both legs, with the right leg tested first, in the order maximal strength, explosive strength and muscular endurance. Participants are asked to avoid strenuous exercise, sleep deprivation, alcohol, caffeine and related medications for 24 hours before testing. Sensations and adverse effects are recorded after the intervention with a transcranial electrical stimulation sensation questionnaire.

Outcomes: Peak torque at 60 degrees per second (maximal strength), average power at 180 degrees per second (explosive strength) and work fatigue during 20 repetitions at 180 degrees per second (muscular endurance) of the right and left knee flexors and extensors.

Sample size: An a priori calculation in G*Power 3.1 for a repeated-measures analysis of variance (effect size f = 0.35, alpha = 0.05, power = 0.80) indicated a minimum of 66 participants. Seventy-five participants (15 per group) are recruited to allow for dropout.

Statistical analysis: Change scores (T1 minus T0) are compared among the five groups with one-way analysis of variance, followed by least significant difference post hoc tests when the omnibus test is significant. Partial eta-squared and Cohen's d are reported as effect sizes. Welch's analysis of variance is used when variances are unequal, and a sensitivity analysis excluding extreme values (beyond three times the interquartile range) is performed. All randomized participants are included in the analysis, and the significance level is set at 0.05.

研究の種類

介入

入学 (実際)

75

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100084
        • Beijing Sport University

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~25年 (大人)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Aged 18 to 25 years
  • College student
  • Physically inactive, defined as fewer than three sessions per week of moderate-intensity exercise lasting at least 30 minutes during the previous 3 months
  • Normal or corrected-to-normal vision, without color blindness, color weakness or dyslexia
  • Able to refrain from strenuous exercise, sleep deprivation, and alcohol, caffeine and related medications for 24 hours before testing
  • Willing to provide written informed consent

Exclusion Criteria:

  • Personal or family history of epilepsy, stroke or other neurological or psychiatric disorders
  • Implanted medical devices or metal implants remaining from surgery
  • Pregnancy
  • Any other contraindication to transcranial direct current stimulation
  • Participation in any other brain stimulation study during the study period

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:基礎科学
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:Accelerated tDCS, 3-minute interval

Two 10-minute sessions of anodal tDCS at 1 mA over the leg area of the primary motor cortex (anode over Cz, cathode over Fpz), separated by a 3-minute interval and delivered once at a single laboratory visit (n = 15).

Anodal transcranial direct current stimulation delivered as two 10-minute sessions at 1 mA within one visit, with an inter-session interval of 3 or 20 minutes according to the assigned arm. Stimulation is delivered with a dual-channel stimulator (TCS-E2, Shenzhen Yingchi Technology Co., Ltd., China) through saline-soaked sponge electrodes (35 cm2), with the anode over Cz and the cathode over Fpz.

他の名前:
  • Accelerated transcranial direct current stimulation; TCS-E2 stimulator
実験的:Accelerated tDCS, 20-minute interval

Two 10-minute sessions of anodal tDCS at 1 mA over the leg area of the primary motor cortex (anode over Cz, cathode over Fpz), separated by a 20-minute interval and delivered once at a single laboratory visit (n = 15).

Anodal transcranial direct current stimulation delivered as two 10-minute sessions at 1 mA within one visit, with an inter-session interval of 3 or 20 minutes according to the assigned arm. Stimulation is delivered with a dual-channel stimulator (TCS-E2, Shenzhen Yingchi Technology Co., Ltd., China) through saline-soaked sponge electrodes (35 cm2), with the anode over Cz and the cathode over Fpz.

他の名前:
  • Accelerated transcranial direct current stimulation; TCS-E2 stimulator
アクティブコンパレータ:Single-session tDCS, 10 minutes

One continuous 10-minute session of anodal tDCS at 1 mA over the leg area of the primary motor cortex (anode over Cz, cathode over Fpz), delivered once at a single laboratory visit (n = 15).

Anodal transcranial direct current stimulation at 1 mA delivered as one continuous session lasting 10 or 20 minutes according to the assigned arm, using the same stimulator, electrodes and montage as the accelerated protocols.

他の名前:
  • Transcranial direct current stimulation; TCS-E2 stimulator
アクティブコンパレータ:Single-session tDCS, 20 minutes

One continuous 20-minute session of anodal tDCS at 1 mA over the leg area of the primary motor cortex (anode over Cz, cathode over Fpz), delivered once at a single laboratory visit (n = 15).

Anodal transcranial direct current stimulation at 1 mA delivered as one continuous session lasting 10 or 20 minutes according to the assigned arm, using the same stimulator, electrodes and montage as the accelerated protocols.

他の名前:
  • Transcranial direct current stimulation; TCS-E2 stimulator
偽コンパレータ:Sham tDCS

Same electrode montage as the active groups. Current is ramped up over 15 seconds and down over 15 seconds (30 seconds in total), and the electrodes remain in place for 10 minutes (n = 8) or 20 minutes (n = 7) to match the duration of the single-session protocols (n = 15).

Sham transcranial direct current stimulation using the same stimulator, electrodes and montage. The current is delivered for 30 seconds (15-second ramp-up and 15-second ramp-down) and then switched off while the electrodes remain in place.

他の名前:
  • 偽経頭蓋直流刺激

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in Peak Torque of the Knee Flexors and Extensors at 60 Degrees per Second
時間枠:Baseline (before stimulation) and immediately after the end of stimulation, on the single study day (Day 1)

Maximal strength is assessed as peak torque (newton-meters) during five consecutive maximal concentric knee flexion-extension cycles at an angular velocity of 60 degrees per second on an isokinetic dynamometer (Biodex System 4 Pro). The right and left knee flexors and extensors are assessed separately, with the right leg tested first. Change is calculated as the post-stimulation value minus the baseline value.

Baseline (before stimulation) and immediately after the end of stimulation, on the single study day (Day 1)
Change in Average Power of the Knee Flexors and Extensors at 180 Degrees per Second
時間枠:Baseline (before stimulation) and immediately after the end of stimulation, on the single study day (Day 1)

Explosive strength is assessed as average power (watts) during five consecutive knee flexion-extension cycles performed with maximal speed and effort at an angular velocity of 180 degrees per second on an isokinetic dynamometer (Biodex System 4 Pro). The right and left knee flexors and extensors are assessed separately. Change is calculated as the post-stimulation value minus the baseline value.

Baseline (before stimulation) and immediately after the end of stimulation, on the single study day (Day 1)
Change in Work Fatigue of the Knee Flexors and Extensors at 180 Degrees per Second
時間枠:Baseline (before stimulation) and immediately after the end of stimulation, on the single study day (Day 1)

Muscular endurance is assessed as work fatigue (percentage) during 20 consecutive knee flexion-extension cycles performed with maximal speed and effort at 180 degrees per second. Work fatigue = (1 - work in the last third of the repetitions / work in the first third) x 100. Higher values indicate greater fatigue. The right and left knee flexors and extensors are assessed separately. Change is calculated as the post-stimulation value minus the baseline value.

Baseline (before stimulation) and immediately after the end of stimulation, on the single study day (Day 1)

二次結果の測定

結果測定
メジャーの説明
時間枠
Number of Participants With Stimulation-Related Adverse Effects
時間枠:Immediately after the end of stimulation, on the single study day (Day 1)

Sensations and adverse effects related to stimulation (for example tingling, itching, burning sensation, headache and fatigue) are recorded with a transcranial electrical stimulation sensation questionnaire after the intervention. The number of participants reporting each adverse effect is summarized by group.

Immediately after the end of stimulation, on the single study day (Day 1)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Rihua Liu, Master's Degree、Beijing Sport University
  • スタディディレクター:Fengxue Qi, doctoral degree、Beijing Sport University

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2025年10月20日

一次修了 (実際)

2025年12月25日

研究の完了 (実際)

2025年12月25日

試験登録日

最初に提出

2026年10月29日

QC基準を満たした最初の提出物

2026年10月29日

最初の投稿 (実際)

2026年11月4日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月4日

QC基準を満たした最後の更新が送信されました

2026年10月29日

最終確認日

2026年10月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 2025391H
  • 2026075 (その他の助成金/資金番号:Fundamental Research Funds for the Central Universities (Beijing Sport University Graduate Innovative Research Project))

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

De-identified individual participant data underlying the results reported in the publication, including demographic characteristics and isokinetic strength outcomes, will be shared.

IPD 共有時間枠

Beginning after publication of the main results.

IPD 共有アクセス基準

Data will be available from the corresponding author (Fengxue Qi, fengxue.qi@hotmail.com) upon reasonable request for non-commercial research purposes, subject to approval of the request and a data use agreement.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する