NCT06262425

Brief Summary

The purpose of this study is to compare the effectiveness of different repetitive Transcranial Magnetic Stimulation protocols for enhancing motor learning in healthy peolple.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 20, 2023

Completed
1 month until next milestone

Study Start

First participant enrolled

January 20, 2024

Completed
27 days until next milestone

First Posted

Study publicly available on registry

February 16, 2024

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2025

Completed
Last Updated

September 2, 2025

Status Verified

August 1, 2025

Enrollment Period

1.5 years

First QC Date

December 20, 2023

Last Update Submit

August 25, 2025

Conditions

Keywords

Transcranial magnetic stimulationMotor learningSomatosensory cortexMotor function

Outcome Measures

Primary Outcomes (1)

  • Change in accuracy

    Accuracy in associating one letter of the keyboard with a letter from the Phoenician alphabet presented in the screen. It will be measured by using the software PsychoPy, that has been used in other studies for measuring motor learning in an indirect way.

    Change from Baseline to 5 days and 10 days in accuracy

Secondary Outcomes (2)

  • Change in reaction time speed

    Change from Baseline to 5 days and 10 days in reaction time speed

  • Change in pegs placed in 30 seconds

    Change from Baseline to 5 days and 10 days in days placed in 30 seconds

Study Arms (3)

repetitive Transcranial Magnetic Stimulation over primary somatosensory cortex

EXPERIMENTAL

Participants in the experimental group will receive 5 weekly sessions of repetitive Transcranial Magnetic Stimulation (rTMS) for two weeks. An excitatory stimulation over the primary somatosensory area corresponding to the dominant hand will be applied. For this purpose, the motor area will be localized and a coil will be placed 2 cm posterior to it. An isolated pulse will be applied to the motor area to ensure that the coil is not placed over the motor area using 110% of the motor resting threshold. After this, 22 trains of 10 Hz at an intensity of 90% of the motor resting threshold will be applied for 4 seconds, with a rest between series of 10 seconds (a total of 880 pulses). After the stimulation, participants will train with the Forced Response training program for a total of 500 correct repetitions and the Purdue Pegboard Test with 4 repetitions for right hand, left hand and both hands.

Device: repetitive Transcranial Magnetic Stimulation over primary somatosensory cortex

repetitive Transcranial Magnetic Stimulation over primary motor cortex

ACTIVE COMPARATOR

Participants in the active comparator group will receive 5 weekly sessions of repetitive Transcranial Magnetic Stimulation (rTMS) for two weeks. An excitatory stimulation over the primary motor cortex corresponding to the dominant hand will be applied. For this purpose, the motor area will be localized, and an isolated pulse will be applied to the motor area to ensure that the coil is placed over the motor area using 100% of the motor resting threshold. After this, 22 trains of 10 Hz at an intensity of 90% of the motor resting threshold will be applied for 4 seconds, with a rest between series of 10 seconds (a total of 880 pulses). After the stimulation, participants will train with the Forced Response training program for a total of 500 correct repetitions and the Purdue Pegboard Test with 4 repetitions for right hand, left hand and both hands.

Device: repetitive Transcranial Magnetic Stimulation over primary motor cortex

Sham repetitive transcranial magnetic stimulation

SHAM COMPARATOR

Participants in the sham group will receive 5 weekly sessions of sham repetitive Transcranial Magnetic Stimulation (rTMS) for two weeks.To achieve the placebo, the localization of the area to be stimulated will be carried out but the coil will be placed in a vertical position so the current will not go through the skull and the patient will just feel the vibration, communicating to the participant that it is likely that during the stimulation process he/she will not feel anything. After the sham stimulation, participants will train with the Forced Response training program for a total of 500 correct repetitions and the Purdue Pegboard Test with 4 repetitions for right hand, left hand and both hands.

Device: sham repetitive Transcranial Magnetic Stimulation

Interventions

It will be applyed a magnetic field over the Somatosensory cortex of the patient that pretends to hiperexcite the membrans of the neurons inthis area to enhance motor learning

repetitive Transcranial Magnetic Stimulation over primary somatosensory cortex

It will be applyed a magnetic field over the primary motor cortex of the patient that pretends to hiperexcite the membrans of the neurons inthis area to enhance motor learning

repetitive Transcranial Magnetic Stimulation over primary motor cortex

It will be applied a sham stimulation with the same protocol that pretends to create the illusion of being stimulated

Sham repetitive transcranial magnetic stimulation

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Older than 18 years old and younger than 65

You may not qualify if:

  • Presenting any neurological pathology
  • Pain during the study
  • Any contraindications to rTMS, such as metal implants, history of epileptic seizures or taking medication that lowers the seizure threshold

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Neuron

Madrid, Madrid, 28045, Spain

Location

Study Officials

  • Alfredo Lerín Calvo, PhD student

    Neuron, Spain

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 20, 2023

First Posted

February 16, 2024

Study Start

January 20, 2024

Primary Completion

July 15, 2025

Study Completion

July 15, 2025

Last Updated

September 2, 2025

Record last verified: 2025-08

Locations