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Not yet recruitingNCT07089056Updated Jul 30, 2025

Effects of Transcranial Direct Current Stimulation After Short-term Immobilization on Motor Learning and Hand Function in Healthy Young Adults

An interventional study of transcranial direct current stimulation and sham transcranial direct current stimulation in Transcranial Direct Current Stimulation, sponsored by Beijing Sport University. Not yet recruiting. Open to participants aged 18 Years to 25 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-30.

Sponsored by Beijing Sport University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 25 Years
Sex
All
01

Study summary

The purpose of the study is to investigate the effects of short-term braking on the motor learning and fine motor skills of healthy adults, and to analyze whether transcranial direct current stimulation can alleviate the effects of braking on motor learning and fine motor skills.

Read the detailed description

The purpose of the study is to investigate the effects of 16-hour short-term immobilization on the motor learning and fine motor skills of healthy adults, and to analyze whether transcranial direct current stimulation intervention can alleviate the effects of immobilization on motor learning and fine motor skills.

02

Conditions studied

  • Transcranial Direct Current Stimulation

Keywords

  • Transcranial direct current stimulation
  • immobilization
  • motor learning
03

In context

Lead sponsor

Beijing Sport University is the lead sponsor of 51 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • (1) age between 18 and 25 years;
  • (2) normal or corrected-to-normal vision;
  • (3) right-handedness.

Exclusion criteria

Exclusion Criteria:

  • (1) with history of pregnancy, cardiovascular disease, other physical impairments or illnesses;
  • (2) with personal or family history of mental illness;
  • (3) implanting any internal or external medical devices;
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Immobilization and Transcranial Direct Current Stimulation

    The participants' right hands will be immobilized for 16 hours, and they will receive 20 minutes of transcranial direct current stimulation before the immobilization period ends.

    Device: sham transcranial direct current stimulation · Procedure: immobilization

  • Experimental
    Immobilization and Sham Transcranial Direct Current Stimulation

    The participants' right hands will be immobilized for 16 hours, and they will receive 20 minutes of transcranial direct current stimulation before the immobilization period ends.

    Procedure: transcranial direct current stimulation · Procedure: immobilization

  • No intervention
    Blank control group

Interventions

  • Proceduretranscranial direct current stimulation

    The intervention will be conducted using a battery-powered stimulator (TCS-E2000, Shenzhen Yingchi Technology Co., Ltd) through a pair of saline-soaked sponge electrodes (5 cm × 5 cm).The stimulation intensity will be set at 2 mA. The stimulation will last for 20 minutes, with a 10 s fade-in period at the start and a 10-s fade-out period at the end of stimulation. The anodal electrode will be placed over the primary motor cortex (M1), and the reference electrode will be positioned at the center of the forehead.

  • Devicesham transcranial direct current stimulation

    The intervention will be conducted using a battery-powered stimulator (TCS-E2000, Shenzhen Yingchi Technology Co., Ltd) through a pair of saline-soaked sponge electrodes (5 cm × 5 cm).The stimulation intensity will be set at 2 mA. The anodal electrode will be placed over the primary motor cortex (M1), and the reference electrode will be positioned at the center of the forehead for 20 minutes. However, there will be current only during the first 10 seconds and the last 10 seconds.

  • Procedureimmobilization

    The researchers will use an upper limb fixation splint to fix the right upper limb of the participants, with the elbow joint flexed at 90 degrees, to ensure that all movements of the wrist, metacarpophalangeal joints, proximal interphalangeal joints, and interphalangeal joints are completely restricted. To avoid discomfort caused by the splint, soft bandages will be wrapped around the hand, and the splint will be adjusted to fit the shape of the hand. Ensure that the fingertips are visible to ensure good blood circulation. The subjects need to wear the upper limb fixation splint for 16 hours. Instruct the subjects to minimize movement and use of the right upper limb as much as possible. During the immobilization process, pay attention to checking if the participants have numbness or other discomfort, as well as whether the blood flow is good. If any adverse symptoms occur, the immobilization will be immediately terminated.

06

What researchers measure

Primary outcomes

  1. Sequence Reaction Time Task

    The participants will sit in front of the laptop and placed their four right fingers on the four keys on the keyboard. In this task, a white circle appears above one of four horizontally arranged white squares on the computer screen with black background. Participans will be instructed to press the proper button on the response pad (buttons H, J, K, L) using the corresponding finger of the right hand (index finger for button H, middle finger for button J, ring finger for button K, and small finger for button L) when the white circle appeared at the left side, middle-left side, middle-right side, or right side of the computer screen, respectively. Each session consists of eight blocks, with each block comprising 120 trials.

    Time frame: Baseline; after one week

Secondary outcomes

  1. Purdue Pegboard Test

    The Purdue Pegboard (model 32020; Lafayette Instrument Co., Lafayette,Indiana) performed the tests. The nail jacks were arranged in two parallel columns, and the nail, washer, and collar were placed in the four cups at the top of the plate before the experiment began. Subjects will be prompted to begin the test by using a nail to jack first with their right hand, then with their left hand, and finally with both hands simultaneously. Each segment was 30 s in duration, and the number of nails transferred by the participant was recorded. Finally, participants will assemble a nail, a washer, a collar and a washer on top of it, starting with their right hand in 1 minute. Each of the above sections was repeated three times to obtain an average score.

    Time frame: Baseline; after one week

  2. Reach and grasp action test

    The reach and grasp test included two parts: the fine grasp test and the gross grasp test. In the fine grip test, participants will be instructed to grasp a pencil with the tips of their thumb and index finger, and in the coarse grip test, they are instructed to grasp a tennis ball with their entire hand. Participants will seat in front of a table, and the tester placed the objects on the marked points. Participants began and ended the grasp task at the same location (30cm from the marker), and all performed the same posture (index finger in contact with thumb). Participants will complete the grasp task 15 times at their own pace. Infrared motion capture system will be used to record 3D kinematic data during the reaching and grasping movements.

    Time frame: Baseline; after one week

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07089056
Lead sponsor
Beijing Sport University
Responsible party
Sponsor
First posted
Jul 28, 2025
Start date
Jul 21, 2025 (estimated)
Primary completion
Sep 15, 2025 (estimated)
Completion
Oct 1, 2025 (estimated)
Last update
Jul 30, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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