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Clinical Trials/NCT03304262
NCT03304262
Completed
Not Applicable

Metaplasticity in the Human Motor Cortex: Validation of an Experimental Design and Comparison of Motor Outcome Measure Sensitivity to Change

University of New Mexico1 site in 1 country13 target enrollmentJuly 18, 2017
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
University of New Mexico
Enrollment
13
Locations
1
Primary Endpoint
Percent Change in MEP Amplitude
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The overall objective is to validate the methodology of a metaplasticity experimental design by assessing change in motor excitability after administration of priming transcranial direct current stimulation (tDCS) followed by repetitive transcranial magnetic stimulation (rTMS) in healthy human participants.

Detailed Description

The overall objective is to validate the methodology of a metaplasticity experimental design by assessing change in motor excitability after administration of priming transcranial direct current stimulation (tDCS) followed by repetitive transcranial magnetic stimulation (rTMS) in healthy human participants. Our primary objective is to compare pre- and post-measures of cortical excitability before priming tDCS (anodal, cathodal or sham) \[M1\], directly after priming tDCS \[M2\], directly after inhibitory rTMS \[M3\], and 10 minutes after inhibitory rTMS \[M4\]. Our secondary objective is to evaluate the sensitivity of motor excitability outcome measures response to the noninvasive neurostimulation (e.g. rTMS and tDCS). We also aim to compare pre- and post- measures of cortical excitability after inhibitory and excitatory priming of the motor cortex, and to evaluate the sensitivity of motor outcome measures to changes in cortical plasticity.

Registry
clinicaltrials.gov
Start Date
July 18, 2017
End Date
March 31, 2018
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sarah Pirio Richardson

Assistant Professor of Neurology

University of New Mexico

Eligibility Criteria

Inclusion Criteria

  • Must be at least 18 years of age (all genders, races, ethnicity)
  • Must have no current psychiatric or neurologic issues
  • Must not have any conditions listed in exclusion criteria
  • Must be fluent in English

Exclusion Criteria

  • History of major psychiatric illness
  • Actively using neuropsychoactive medication
  • Legal or mental incompetency
  • Substance use disorder, abuse or dependence, with active use within the last three months
  • Significant medical or neurological illness
  • Prior neurosurgical illness
  • Prior neurosurgical procedure
  • History of seizure
  • History of ECT or TMS treatment within the past there months
  • Presence of a pacemaker, implanted medical pump or device, metal plate, or metal object in skull or eye (including shunts, dental implants, facial tattoos with metallic ink)

Outcomes

Primary Outcomes

Percent Change in MEP Amplitude

Time Frame: assessed and reported throughout study completion pre- and post- intervention approximately 30 minutes

Percent Change in MEP amplitude over the first dorsal interosseous (FDI) muscle of the right hand

Secondary Outcomes

  • Cortical Silent Period(tDCS + rTMS assessed and reported pre and post (approximately 10 minutes))
  • Simple Reaction Time(The final outcome will be percent change in the reaction time from pre- to post- intervention.)

Study Sites (1)

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