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Performance Enhancement and Non-Invasive Brain Stimulation

Performance Enhancement and Non-Invasive Brain Stimulation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02498574
Enrollment
121
Registered
2015-07-15
Start date
2016-08-31
Completion date
2018-08-31
Last updated
2019-08-02

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

Conditions

Brain Stimulation, Executive Function, Motor Activity

Brief summary

A promising form of enhancing brain function non-invasively involves stimulating the brain using weak magnetic or electric currents. This method is becoming increasingly popular in both clinical and commercial circles; a number of portable, at-home devices are available on the commercial market for personal use. In this study, the investigators aim to determine factors associated with the enhancement of cognitive and motor learning following transcranial direct-current stimulation in healthy young adults. Understanding how participants respond to brain stimulation is critical to maximizing the effectiveness of stimulation and determining its potential as a performance-enhancing aid for mental tasks. Future developments of this study may also inform the capacity of brain stimulation to act as non-drug alternative to treatment for cognitive decline.

Detailed description

This study involves a single session of anodal tDCS, applied over the motor cortex, while performing a task of motor dexterity. Pre and post stimulation evaluations will assess any effects of the stimulation on motor and cognitive performance.

Interventions

DEVICETranscranial Direct Current Stimulation

Non-invasive brain stimulation applied to the surface of the scalp

BEHAVIORALWorking Memory Training

Cognitively challenging game played concurrently with transcranial direct-current stimulation

Sponsors

Bruyère Health Research Institute.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants must be in good health, * between 18-35 years of age * with no prior history of neurological diseases such as multiple sclerosis, Parkinson's disease, stroke with paralysis.

Exclusion criteria

* Participants with cardiac stimulators (pace-makers) and those with metal implants in the skull will be excluded. * Pregnant women will also be excluded. Participants will be required to fill out a brief health questionnaire to ensure that they have no conditions that would prevent brain stimulation.

Design outcomes

Primary

MeasureTime frameDescription
Change in ratings on cognitive training surveyBaseline, Post-test following 20-minute stimulation periodThis survey aims to assess participant perceptions on brain stimulation, and includes a series of related questions, rated on a scale of 1-7.
Change in cognitive performanceBaseline, Post-test following 20-minute stimulation periodWe will measure changes in cognitive performance on neuropsychological tests.
Change in game performanceBaseline, Post-test following 20-minute stimulation periodWe will measure changes in performance on a cognitively-challenging game performed concurrently with the non-invasive brain stimulation.
Change in motor performanceBaseline, Post-test following 20-minute stimulation periodWe will measure changes in motor performance on the Grooved Pegboard task.

Countries

Canada

Outcome results

None listed

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