Performance Enhancement and Non-Invasive Brain Stimulation

NCT ID: NCT02498574

Last Updated: 2019-08-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

121 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-08-31

Study Completion Date

2018-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Executive Function Motor Activity Brain Stimulation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group 1

Non-invasive brain stimulation protocol expected to improve performance, with cognitively challenging game

Group Type EXPERIMENTAL

Transcranial Direct Current Stimulation

Intervention Type DEVICE

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

Working Memory Training

Intervention Type BEHAVIORAL

Cognitively challenging game played concurrently with transcranial direct-current stimulation

Group 2

Non-invasive brain stimulation protocol not expected to improve performance, with cognitively challenging game

Group Type PLACEBO_COMPARATOR

Transcranial Direct Current Stimulation

Intervention Type DEVICE

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

Working Memory Training

Intervention Type BEHAVIORAL

Cognitively challenging game played concurrently with transcranial direct-current stimulation

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Transcranial Direct Current Stimulation

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

Intervention Type DEVICE

Working Memory Training

Cognitively challenging game played concurrently with transcranial direct-current stimulation

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Bruyère Health Research Institute.

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Sheida Rabipour, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Ottawa

Francois Tremblay, PT, PhD

Role: PRINCIPAL_INVESTIGATOR

Bruyere Continuing Care

Patrick SR Davidson, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Ottawa

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Bruyere Continuing Care

Ottawa, Ontario, Canada

Site Status

Bruyere Research Institute

Ottawa, Ontario, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

M16-15-015

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Effects of tDCS on Cognition in MCI: A RCT
NCT05584748 NOT_YET_RECRUITING NA