Actively Recruiting
Repetitive Transcranial Magnetic Stimulation Primed Self-controlled Practice on Motor Learning
Led by National Taiwan University Hospital · Updated on 2025-09-29
72
Participants Needed
1
Research Sites
173 weeks
Total Duration
On this page
Sponsors
N
National Taiwan University Hospital
Lead Sponsor
N
National Science and Technology Council, Taiwan
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to investigate the additive effects of combining self-controlled practice with repetitive transcranial magnetic stimulation (rTMS) pretreatment on motivation enhancement and motor learning performance in healthy young adults. According to the "Optimizing Performance Through Intrinsic Motivation and Attention for Learning" (OPTIMAL) theory, numerous studies have demonstrated that providing learners with autonomy during practice can facilitate intrinsic motivation and motor learning. However, self-controlled practice alone may have limited effects, and further interventions may be required to amplify learning outcomes. In recent years, non-invasive brain stimulation techniques-particularly high-frequency (facilitatory) rTMS applied to the dorsolateral prefrontal cortex (DLPFC)-have been shown to enhance motivational drive and explicit learning performance by strengthening the connectivity of the DLPFC-midbrain dopamine pathway. For example, 10 Hz high-frequency stimulation can significantly improve learners' accuracy and motivation. Interestingly, several sequence learning studies have found that low-frequency (inhibitory) rTMS, when used as a priming intervention, can instead enhance implicit procedural learning. This effect may occur because inhibiting the lateral prefrontal cortex reduces its top-down suppression of implicit learning systems, thereby releasing procedural learning potential. Based on the theory of metaplasticity, applying facilitatory or inhibitory stimulation beforehand can alter the threshold of synaptic plasticity, thus influencing subsequent learning outcomes. Therefore, this study designed two DLPFC pretreatments-facilitatory and inhibitory-and combined them with self-controlled practice to systematically examine the interaction between different stimulation protocols on motivation and motor learning. This cross-sectional experiment plans to recruit 72 healthy participants aged 20 or older, randomly assigned to one of six groups: (1) facilitatory rTMS + self-controlled practice, (2) facilitatory rTMS + yoked control, (3) inhibitory rTMS + self-controlled practice, (4) inhibitory rTMS + yoked control, (5) sham rTMS + self-controlled practice, and (6) sham rTMS + yoked control. The experiment will last for seven days. On Day 1, participants will complete baseline testing, followed by facilitatory rTMS, inhibitory rTMS, or sham stimulation over the DLPFC. Immediately afterward, they will engage in a trajectory-tracking learning task (manipulating a joystick to reproduce a sine-wave pattern). After practice, participants will complete a motivation assessment. During the trajectory-tracking task, the self-controlled group can choose when to receive feedback to adjust their learning, whereas the yoked control group will receive feedback at time points matched to their paired counterpart. On Day 2, participants will again receive the assigned rTMS (facilitatory, inhibitory, or sham), complete the trajectory-tracking task, and undergo a motivation assessment. After a five-minute rest, they will perform retention and transfer tests, followed by TMS measurement of cortical excitability. On Day 7, participants will return to the laboratory to complete another retention and transfer test, along with cortical excitability measurement via TMS. The primary behavioral outcomes are the root mean square error (RMSE) and error estimation (EE) in the trajectory-tracking task. Motivation will be assessed using the Intrinsic Motivation Inventory (IMI). As there have been no prior studies combining DLPFC rTMS pretreatment with practice autonomy, the results of this experimental design are expected to provide new insights and references for enhancing motor learning ability in healthy adults.
CONDITIONS
Official Title
Repetitive Transcranial Magnetic Stimulation Primed Self-controlled Practice on Motor Learning
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy adults aged 18-35 years
- Right-handed according to Edinburgh Handedness Inventory
- Normal or corrected-to-normal vision and hearing
- Eligible for non-invasive brain stimulation with no contraindications to TMS
- Able to understand study procedures and provide written informed consent in Chinese
- Willing to comply with all study visits and tasks including TBS/rTMS and motor practice
- For yoked pairing: able to be matched to a counterpart participant for practice parameters
You will not qualify if you...
- History of epilepsy, seizures, or unexplained fainting; family history of epilepsy in first-degree relatives
- Presence of intracranial metal or implanted medical devices such as cochlear implants, deep brain stimulators, or aneurysm clips; non-removable metallic objects in head or neck
- Cardiac pacemaker or other implanted electronic devices
- Current or past major neurological or psychiatric disorders including stroke, traumatic brain injury, multiple sclerosis, major depression, bipolar disorder, or schizophrenia
- Current use of medications that lower seizure threshold or affect cortical excitability, unstable psychotropic regimens
- Active migraine with aura or chronic severe headaches
- Pregnancy, planning pregnancy during participation, or breastfeeding if site policy excludes
- Substance or alcohol use disorder within past 12 months; positive alcohol or drug screen on visit days
- Sleep deprivation less than 5 hours the day before stimulation or excessive caffeine intake (more than 400 mg) within 6 hours before stimulation
- Skin conditions or open wounds at stimulation or electrode sites
- Prior extensive training on the specific motor task used in the study
- Concurrent participation in another interventional study or brain stimulation received within past 3 months
- Any condition judged by investigators to make participation unsafe or data unreliable
AI-Screening
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Trial Site Locations
Total: 1 location
1
National Taiwan University Hospital
Taipei, Taiwan, 100
Actively Recruiting
Research Team
M
Min Tse Lee, bachelor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
6
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