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Clinical Trials/NCT03481309
NCT03481309
Completed
N/A

Modulation of Motor Cortex Excitability by Transcranial Magnetic Stimulation and Transcranial Direct Current Stimulation

University of North Carolina, Chapel Hill1 site in 1 country19 target enrollmentAugust 24, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Motor Activity
Sponsor
University of North Carolina, Chapel Hill
Enrollment
19
Locations
1
Primary Endpoint
Changes in Motor-evoked Potentials Ratios
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Investigating modulation of motor cortex excitability by transcranial magnetic stimulation and transcranial direct current stimulation.

Detailed Description

Purpose of this pilot study is to modulate the motor cortex excitability by transcranial magnetic stimulation and transcranial direct current stimulation. Electromyography will be recorded on right abductor digiti minimi muscle to find the motor threshold and measure motor evoked potentials for each healthy participant. In addition, electroencephalography (EEG) data will be collected on the scalp with a high-density EEG net. Eighteen healthy participants will be in this study. Each participant will be seated in a reclining chair and applied non-invasive magnetic and electrical stimulations on the scalp. At baseline, the participant's resting motor threshold (RMT) will be estimated by adjusting the intensity of TMS applied on the left motor cortex to achieve motor-evoked potentials of about 50 uV with 10 TMS pulses at a rate of 0.25 Hz. Then a 3-condition, 3-session, 6-sequence randomized crossover experiment will be used to characterize and compare three versions of tDCS stimulation: anode, cathode, sham. Before and after a 10-min tDCS condition is applied, TMS pulses at 120% of RMT intensity will be applied for 10 minutes and TMS-evoked potential and motor-evoked potential amplitudes will be measured. Each session has at least 1-day gap to remove outlasting effects. We will also be collecting structural magnetic resonance imaging (sMRI) to target primary motor cortex precisely.

Registry
clinicaltrials.gov
Start Date
August 24, 2018
End Date
February 1, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Between the ages of 18 and 35
  • Right-handed
  • Capacity to understand all relevant risks and potential benefits of the study (informed consent)
  • Willing to comply with all study procedures and be available for the duration of the study
  • Speak and understand English

Exclusion Criteria

  • Prior concussion
  • Diagnosis of eating disorder (current or within the past 6 months)
  • Diagnosis of obsessive compulsive disorder (lifetime)
  • Attention-deficit/hyperactivity disorder (currently under treatment)
  • Neurological disorders and conditions, including, but not limited to:
  • History of epilepsy
  • Seizures (except childhood febrile seizures and electroconvulsive therapy-induced seizures)
  • History of stroke
  • Parkinson's disease
  • Multiple sclerosis

Outcomes

Primary Outcomes

Changes in Motor-evoked Potentials Ratios

Time Frame: right before and after 2mA tDCS stimulation for 10 minutes at each session

The investigators will record motor-evoked potentials and calculate changes in between before and after 2mA tDCS stimulation for 10 minutes.

Changes in TMS-evoked Potentials Ratios

Time Frame: right before and after 2mA tDCS stimulation for 10 minutes at each session

The investigators will record TMS-evoked potentials using EEG and calculate changes in between before and after 2mA tDCS stimulation for 10 minutes.

Secondary Outcomes

  • Changes in Resting-state EEG Dynamics Ratios(4 minutes recordings before and after each 2mA tDCS stimulation for 10 minutes at each session)

Study Sites (1)

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