Developing and Optimizing Transcranial Magnetic Stimulation for Motor Rehabilitation

June 2, 2026 updated by: Elisa Kallioniemi
This study aims to evaluate three different transcranial magnetic stimulation protocols and their impact on motor system neurophysiology and skill learning.

Study Overview

Status

Withdrawn

Detailed Description

Transcranial magnetic stimulation (TMS) is a non-invasive brain stimulation method that induces long-term changes in connections between neuronal networks. This and the ability to activate the whole motor system allows the use of TMS to facilitate motor recovery. The motor system has different excitatory states associated with ongoing mu oscillation. Here, the investigators will monitor brain mu oscillations in real-time non-invasively using electroencephalography and modulate the function of the motor system. The investigators will test the impact of three different TMS protocols on motor system neurophysiology and skill learning. These data will provide novel understanding needed to improve TMS approaches for individuals requiring motor rehabilitation.

Study Type

Interventional

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 18-40 years old
  • Able to read, understand, and sign the informed consent in English
  • Right-handed

Exclusion Criteria:

  • A sensory or physical impairment
  • History of epilepsy or seizures in the family
  • Non-removable metal or electronics (e.g., a cochlear implant, cardiac pacemaker, or implanted electronic devices) in your head or body
  • A head injury with loss of consciousness
  • Diagnosis of psychiatric or neurological disorder
  • Skin defects or active infections on the scalp or hands
  • Pregnancy or breastfeeding

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Single-pulse TMS over the primary motor cortex
We will administer single-pulse TMS to the primary motor cortex while measuring motor responses and just before a skill-learning task.
Transcranial magnetic stimulation (TMS) is a non-invasive brain stimulation method that can induce long-term changes in connections between neuronal networks.
Experimental: Paired-pulse TMS over the primary motor cortex
We will administer paired-pulse TMS to the primary motor cortex while measuring motor responses and just before a skill-learning task.
Transcranial magnetic stimulation (TMS) is a non-invasive brain stimulation method that can induce long-term changes in connections between neuronal networks.
Sham Comparator: Sham TMS over the primary motor cortex
We will administer sham TMS to the primary motor cortex while measuring motor responses and before a skill-learning task.
Transcranial magnetic stimulation (TMS) is a non-invasive brain stimulation method that can induce long-term changes in connections between neuronal networks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effect of TMS on motor evoked potentials
Time Frame: Up to 1 second after TMS
Amplitude of the motor evoked potentials in millivolts.
Up to 1 second after TMS
Skill learning accuracy
Time Frame: Up to 12 minutes
Skill learning accuracy as the total number of correct responses.
Up to 12 minutes
Skill learning speed
Time Frame: Up to 12 minutes
Skill learning speed in seconds.
Up to 12 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Elisa Kallioniemi, Ph.D., New Jersey Institute of Technology

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

July 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

April 27, 2023

First Submitted That Met QC Criteria

May 6, 2023

First Posted (Actual)

May 16, 2023

Study Record Updates

Last Update Posted (Actual)

June 4, 2026

Last Update Submitted That Met QC Criteria

June 2, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • IRB_2303032088

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Preprocessed and anonymized data will be provided upon request to the faculty / research staff of recognized research, medical, and educational institutions for educational and scientific purposes.

IPD Sharing Time Frame

Data will be shared only upon request after the study has ended (within 6 months).

IPD Sharing Access Criteria

To receive access, the study investigators must be contacted via an institutional e-mail.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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