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Primed vs Unprimed Facilitatory and Depressive Paired Associative Stimulation

Primed vs Unprimed Facilitatory and Depressive Paired Associative Stimulation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02619643
Enrollment
32
Registered
2015-12-02
Start date
2015-12-31
Completion date
2017-12-31
Last updated
2019-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

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.

Interventions

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
DEVICE_FEASIBILITY
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline peak-to-peak amplitude of motor evoked potentialImmediately before and within 60 minutes following interventionSingle-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.
Change from baseline resting motor thresholdImmediately before and within 60 minutes following interventionSingle-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.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026