Cortical Excitability

6

Review clinical trials related to Cortical Excitability. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Frequency-Dependent Effects of Transcranial Photobiomodulation With Same Peak Irradiance on Cortical Excitability and Fine Motor Performance

This study investigates the frequency-dependent neuromodulatory effects of transcranial photobiomodulation (tPBM) over the primary motor cortex (M1) on cortical excitability and fine motor performance in healthy young adults. Using a randomized, double-blind, sham-controlled, 5-arm crossover design, 20 healthy participants will undergo five experimental conditions separated by a mandatory 7-day washout period: Continuous Wave (CW), 10 Hz pulsed tPBM, 40 Hz pulsed tPBM, 100 Hz pulsed tPBM, and a Sham control. To isolate pulse frequency while holding peak intensity constant, all active interventions will utilize an identical peak irradiance, with pulsed modes operating at a 50% duty cycle (delivering 50% of the cumulative energy dose relative to CW). Primary outcomes include corticospinal excitability measured via single- and paired-pulse Transcranial Magnetic Stimulation (TMS), alongside fine motor speed and dexterity assessed via a computerized finger-tapping task.

Participants needed: 20
Trial details
Phase: Phase 1Age: 18-35Biological sex: AllType: InterventionalSponsor: Hospital de Clinicas de Porto AlegreUpdated: Aug 7, 2026Locations: 1
Eligibility criteria

Voluntary Participation: Participants who are clear of their cognitive faculties... [+2]

Use of any continuous psychotropic medication within the past 12 months. [+6]

Status: Not yet recruiting

Frequency-Dependent Effects of Transcranial Photobiomodulation on Cortical Excitability

This study aims to investigate the frequency-dependent effects of near-infrared (NIR) transcranial photobiomodulation (tPBM) on human cortical excitability and fine motor performance. A cohort of 20 healthy adult volunteers (aged 18-35 years) will participate in a randomized, double-blind, sham-controlled, single-center study utilizing a within-subject, five-arm crossover design. Each participant will undergo five distinct experimental conditions separated by a strict washout period: active Continuous Wave (CW) tPBM, active pulsed tPBM at three neural oscillation frequencies (10 Hz, 40 Hz, and 100 Hz), and an inactive Sham comparator. All interventions will be delivered using a clinical-grade near-infrared device. To isolate the specific effects of pulse frequency from overall energy delivery, the total energy dose (cumulative Joules) and total exposure time will be held perfectly constant across all active arms. The pulsed conditions will keeps the average irradiance and cumulative fluence identical to the continuous wave mode. Cortical excitability will be assessed via single- and paired-pulse Transcranial Magnetic Stimulation (TMS) protocols over the primary motor cortex (M1). Fine motor performance will be quantified using a smartphone-based Finger Tapping Test (FTT). Safety and systemic parameters will be tracked using the Systematic Assessment for Treatment Emergent Events - Systematic Inquiry (SAFTEE-SI) and vital signs. The central hypothesis is that distinct modulation frequencies will differentially influence corticospinal excitability and motor execution, independent of the total energy delivered.

Participants needed: 20
Trial details
Phase: Phase 1Age: 18-35Biological sex: AllType: InterventionalSponsor: Hospital de Clinicas de Porto AlegreUpdated: Jul 28, 2026Locations: 1
Eligibility criteria

Voluntary Participation: Participants who are clear of their cognitive faculties... [+2]

Use of any continuous psychotropic medication within the past 12 months. [+6]

Status: Not yet recruiting

Assessing the Effects of Hormones on Noninvasive Transcranial Stimulation

This study is investigating how two types of non-invasive brain stimulation, transcranial electrical stimulation (TES) and transcranial magnetic stimulation (TMS), affect brain activity, and whether combining them produces stronger or more consistent effects than either one used alone. The motivation for this comes from the observation that TMS, which is FDA-approved for treating depression, tends to work less well in postmenopausal women because lower estrogen levels reduce the brain's ability to respond to stimulation. The research team believes that pairing TMS with TES, which targets a different set of brain cells, may be able to overcome this hormonal barrier and make stimulation more effective. Participants will come into the lab for up to 24 visits over 8 months, beginning with an initial visit to establish the right stimulation settings, followed by a series of stimulation sessions in which brain activity is measured before and after receiving either TES, TMS, or both together. For female participants, sessions will be scheduled at specific points in the menstrual cycle to capture the natural monthly rise and fall of estrogen, while male participants will be scheduled on a comparable fixed interval as a comparison group. The insights gained from this study could directly inform the development of better, more reliable brain stimulation treatments for women with depression.

Participants needed: 25
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Carnegie Mellon UniversityUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Age between 18 and 40 years old [+1]

Allergies to henna [+7]

Status: Recruiting

rTMS Induced Reduction in M1 Excitability

When learning a new skill, much of the improvement comes from small alterations the brain makes with each repetition during practice, but this isn't the only time that improvements are made during the learning process. Individuals also get better at the motor skills during the time between practices, through a process called "consolidation." It is known that an area of the brain called the primary motor cortex is involved in learning during active practice, but the investigators want to study if the primary motor cortex is important for consolidation. The investigators will examine how lowering the activity in this brain region affects your ability to consolidate learning to play a song on the videogame Guitar Hero.

Participants needed: 32
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Indiana UniversityUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Between ages 18 and 45 years old (to avoid any changes in the developing brain,... [+3]

Currently prescribed and taking stimulant medication (Adderall, Ritalin, Vyvanse... [+3]

Status: Recruiting

Dual-task Training Combined With tDCS on Cognitive-motor Performance and Brain Activity in Stroke Patients

The purpose of this study is to evaluate tDCS combined with cognitive-motor training on dual-task interference during dual-task walking, dual-task foot pedaling and the corresponding alterations of brain activity.

Participants needed: 72
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: The Hong Kong Polytechnic UniversityUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

a diagnosis of stroke, stroke onset of more than 6 months, [+5]

neurological disorders, gait-precluding pain or comorbidity, [+6]

Status: Not yet recruiting

Cortical Excitability and Role of Non Invasive Brain Stimulation in ADHD and AUTISM

This double-blind, randomized, sham-controlled clinical trial will evaluate the effects of repetitive transcranial magnetic stimulation (rTMS) on children and adolescents with attention-deficit/hyperactivity disorder (ADHD) or autism spectrum disorder (ASD) and matched healthy controls. Participants aged 6-19 years will be assigned to active or sham rTMS protocols targeting the dorsolateral prefrontal cortex over 3 weeks, with assessment of changes in disorder-specific symptoms and cortical excitability. The study aims to determine the safety, feasibility, and preliminary efficacy of rTMS as a non-invasive neuromodulation approach in pediatric neurodevelopmental disorders.

Participants needed: 80
Trial details
Age: 6-19Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: Jan 2, 2026
Eligibility criteria

Age 6-19 years. [+4]

Epilepsy or seizure history. [+3]