Muscle StrengthACC-tDCSNCT07916207
Acute Effects of Accelerated Transcranial Direct Current Stimulation on Leg Muscle Strength in Physically Inactive College Students
A study testing Accelerated anodal tDCS and Single-session anodal tDCS in people with Muscle Strength and Sedentary Behaviors, run by Beijing Sport University at 1 site in China.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 to 25 yearsHealthy volunteers can take part
- Conditions the study is for
- Muscle Strength, Sedentary Behaviors
- What is being tested?
- Accelerated anodal tDCS and Single-session anodal tDCS
- Type of treatment
- Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 75 participants
- Where
- 1 siteChina
- Study dates
- 20 Oct 2025to 25 Dec 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 25 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
About this study
Official title: 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:
Read more
- 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
Read the detailed description
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.
- Conditions
- Muscle Strength, Sedentary Behaviors
- Being tested
- Accelerated anodal tDCS, Single-session anodal tDCS, Sham tDCS
- Keywords
- Transcranial Direct Current Stimulation, Accelerated Stimulation Protocol, Inter-Session Interval Primary, Primary Motor Cortex, Isokinetic Dynamometry, Explosive Strength, Muscular Endurance
- Medical subject headings
- Sedentary Behavior
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Accelerated anodal tDCSDevice
Also called Accelerated transcranial direct current stimulation; TCS-E2 stimulator
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.
Single-session anodal tDCSDevice
Also called Transcranial direct current stimulation; TCS-E2 stimulator
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.
Sham tDCSDevice
Also called Sham transcranial direct current stimulation
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.
| Study group | Role | What they receive |
|---|---|---|
| Accelerated tDCS, 3-minute interval | Experimental | 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). Receives: Device: Accelerated anodal tDCS |
| Accelerated tDCS, 20-minute interval | Experimental | 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). Receives: Device: Accelerated anodal tDCS |
| Single-session tDCS, 10 minutes | Active comparator | 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). Receives: Device: Single-session anodal tDCS |
| Single-session tDCS, 20 minutes | Active comparator | 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). Receives: Device: Single-session anodal tDCS |
| Sham tDCS | Sham comparator | 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). Receives: Device: Sham tDCS |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Peak Torque of the Knee Flexors and Extensors at 60 Degrees per Second
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.
Measured: 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
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.
Measured: 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
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.
Measured: Baseline (before stimulation) and immediately after the end of stimulation, on the single study day (Day 1)
Secondary outcomes (1)
Number of Participants With Stimulation-Related Adverse Effects
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.
Measured: Immediately after the end of stimulation, on the single study day (Day 1)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Nov 2026
- Study start20 Oct 2025
- Primary completion25 Dec 2025
- Study completion25 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Muscle StrengthStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Five-arm, parallel-group design. Participants are randomly allocated in a 1:1:1:1:1 ratio, with randomization stratified by sex.
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 75 participants (actual)
Sponsor and investigators
- Lead sponsor
- Beijing Sport University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Rihua Liu, Master's Degree, Principal investigator, Beijing Sport UniversityFengxue Qi, doctoral degree, Study director, Beijing Sport University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07916207
- Sponsor's protocol ID
- 2025391H
- Other IDs
- 2026075
- Acronym
- ACC-tDCS
- Status last verified
- Oct 2026
- First submitted
- 29 Oct 2026
- Last updated
- 4 Nov 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: De-identified individual participant data underlying the results reported in the publication, including demographic characteristics and isokinetic strength outcomes, will be shared.
Study at a glance
From the registry record, last updated by the sponsor on 4 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- 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
- ClinicalTrials.gov ID
- NCT07916207
- Acronym / sponsor ID
- ACC-tDCS / 2025391H
- Conditions
- Muscle Strength, Sedentary Behaviors
- Keywords
- Transcranial Direct Current Stimulation, Accelerated Stimulation Protocol, Inter-Session Interval Primary, Primary Motor Cortex, Isokinetic Dynamometry, Explosive Strength, Muscular Endurance
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 75 participants (actual)
- Lead sponsor
- Beijing Sport UniversityUniversity, hospital or other
- Study start
- 20 Oct 2025 (actual)
- Primary completion
- 25 Dec 2025 (actual)
- Study completion
- 25 Dec 2025 (actual)
- First posted
- 4 Nov 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
Detailed description
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.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 5
- Model description
- Five-arm, parallel-group design. Participants are randomly allocated in a 1:1:1:1:1 ratio, with randomization stratified by sex.
| Arm | Type | Receives |
|---|---|---|
| Accelerated tDCS, 3-minute interval | Experimental | Device: Accelerated anodal tDCSTwo 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). |
| Accelerated tDCS, 20-minute interval | Experimental | Device: Accelerated anodal tDCSTwo 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). |
| Single-session tDCS, 10 minutes | Active comparator | Device: Single-session anodal tDCSOne 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). |
| Single-session tDCS, 20 minutes | Active comparator | Device: Single-session anodal tDCSOne 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). |
| Sham tDCS | Sham comparator | Device: Sham tDCSSame 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). |
Who may qualify
- Ages
- 18 to 25 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (5 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Accelerated anodal tDCSAlso: Accelerated transcranial direct current stimulation; TCS-E2 stimulatorAnodal 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. | Device | Accelerated tDCS, 20-minute interval, Accelerated tDCS, 3-minute interval |
| Single-session anodal tDCSAlso: Transcranial direct current stimulation; TCS-E2 stimulatorAnodal 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. | Device | Single-session tDCS, 10 minutes, Single-session tDCS, 20 minutes |
| Sham tDCSAlso: Sham transcranial direct current stimulationSham 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. | Device | Sham tDCS |
Primary outcome
Change in Peak Torque of the Knee Flexors and Extensors at 60 Degrees per Second
Time frame: 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.
Change in Average Power of the Knee Flexors and Extensors at 180 Degrees per Second
Time frame: 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.
Change in Work Fatigue of the Knee Flexors and Extensors at 180 Degrees per Second
Time frame: 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.
1 secondary outcome
Number of Participants With Stimulation-Related Adverse Effects
Time frame: Immediately after the end of stimulation, on the single study day (Day 1)
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Nov 2026.
- Individual participant dataSharing planned: Yes. De-identified individual participant data underlying the results reported in the publication, including demographic characteristics and isokinetic strength outcomes, will be shared.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Rihua Liu, Master's Degree principal investigator
Beijing Sport University
Fengxue Qi, doctoral degree study director
Beijing Sport University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Accelerated anodal tDCS and Single-session anodal tDCS in people with Muscle Strength and Sedentary Behaviors, run by Beijing Sport University at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Peak Torque of the Knee Flexors and Extensors at 60 Degrees per Second (time frame: Baseline (before stimulation) and immediately after the end of stimulation, on the single study day (Day 1)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Nov 2026.