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Clinical Trials/NCT02619643
NCT02619643
Completed
Not Applicable

Primed vs Unprimed Facilitatory and Depressive Paired Associative Stimulation

University of Minnesota0 sites32 target enrollmentDecember 2015
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
University of Minnesota
Enrollment
32
Primary Endpoint
Change from baseline resting motor threshold
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Following brain injury (e.g. stroke), application of non-invasive brain stimulation may improve rehabilitative efforts. However, the most effective method of non-invasive brain stimulation is unknown. Paired associative stimulation (PAS) is a method of non-invasive brain stimulation that pairs an electrical peripheral nerve stimulus with a magnetic stimulus to the head. This method can be applied in a manner that increases (facilitates) or decreases (depresses) excitability within the brain. Furthermore, applying two consecutive PAS sessions within minutes of each other (called primed PAS) may augment changes in excitability more than a single PAS session alone.

Thus, the purpose of this study is to compare the effect of a double PAS session (primed PAS) to the effect of a single PAS session (unprimed PAS) and a sham PAS session in healthy individuals.

Registry
clinicaltrials.gov
Start Date
December 2015
End Date
December 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • ≥ 18 and ≤ 30 years of age
  • Elicitable motor evoked potential from the motor cortex contralateral to the dominant hand
  • Elicitable N20 sensory evoked potential

Exclusion Criteria

  • History of neurological disease
  • Seizure within the past 2 years
  • Currently taking epileptogenic medication
  • Peripheral neuropathy
  • Cognitive impairment and/or major psychiatric disorder
  • Metal in the head (dental permitted)
  • Pacemaker or other indwelling devices
  • Pregnancy

Outcomes

Primary Outcomes

Change from baseline resting motor threshold

Time Frame: Immediately before and within 60 minutes following intervention

Single-pulse TMS will be used to evoke a motor response that is recorded using electromyography (EMG). The lowest stimulator output needed to elicit a consistent response will be recorded.

Change from baseline peak-to-peak amplitude of motor evoked potential

Time Frame: Immediately before and within 60 minutes following intervention

Single-pulse TMS will be used to evoke a motor response that is recorded using electromyography (EMG). The peak-to-peak amplitude of the EMG response will be measured.

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