Non-Invasive Brain-Computer Interface for Virtual Object Control

NCT ID: NCT02071485

Last Updated: 2018-01-18

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

Total Enrollment

205 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-03-31

Study Completion Date

2018-01-08

Brief Summary

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

A brain-computer interface (BCI) is a system that provides a separate output pathway for neurological signals whereby they can be interpreted to determine the user's intended cognitive action. Utilizing EEG-based sensorimotor rhythms (SMRs) generated in the motor cortex has allowed subjects to control virtual computer cursors in up to three dimensions by simply imagining the movement of a specified body part. Nevertheless, the scalp EEG signals are smeared by the volume conduction effect and measurement noise. The overall hypothesis of this study is that EEG-based virtual object control may help reveal optimal motor imagination tasks best used in a BCI.

The PI's hypotheses include: (1) The use of advanced signal processing techniques will better reveal characteristics of EEG signals that represent the underlying motor cognitive function of the subject; (2) BCI systems based on SMR generated using motor imaginations will allow effective control of a virtual object in real time; (3) EEG imaging techniques will provide insight into the areas of cortical activation during a motor imagery task that can be utilized to increase the spatial resolution of non-invasive BCI's.

Detailed Description

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

The goal of the present study is to explore advanced signal processing techniques that will better reveal characteristics of EEG signals that represent the underlying motor cognitive function of the subject, and conduct experiments to better control an virtual object on the computer screen including a cursor or a helicopter.

The primary objective of this study is to test the above hypotheses (1) and (2) in a healthy subject population.This study will determine the ability of subjects with full cognitive function to control a non-invasive brain-computer interface by imagining a particular movement. Using non-invasive methods, we will investigate the neural processes that occur during the motor imagination tasks associated with controlling a virtual object. Using a variety of motor imaginations, we will determine which tasks are best used for BCI control by quantitative means of BCI performance and neurological dynamic system analysis.

Subjects for this study will be healthy, English speaking adult volunteers (18-64 years old) with no history of mental illness, neurological deficit, or traumatic brain injury.

Conditions

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

Individuality

Study Design

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

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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

No treatment

Subjects in this study will receive no treatment and rather will only be trained in using the motor imagination-based BCI system

No interventions assigned to this group

Eligibility Criteria

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

Inclusion Criteria

* Between the age of 18 and 64

Exclusion Criteria

* History of traumatic brain injury/brain lesion, neurological deficit or neurodegenerative disorder
Minimum Eligible Age

18 Years

Maximum Eligible Age

64 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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

University of Minnesota

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.

Bin He, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Minnesota

Locations

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

Nils Hasselmo Hall at the University of Minnesota - Twin Cities campus

Minneapolis, Minnesota, United States

Site Status

Countries

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

United States

Other Identifiers

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

1312M46726

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

Feasibility of Stimulating the Visual Cortex in Blind
NCT02747589 ACTIVE_NOT_RECRUITING NA