EEG-based Brain-computer Interface Database for Motor Rehabilitation

February 28, 2025 updated by: Jaime Alejandro Quiroga Forero

Deep Dictionaries for Feature Extraction in Context of Sparse Data for Electroencephalographic Signals from Brain-computer Interfaces

The human brain, as a processing center, controls bodily, cognitive, emotional and social functions, enabling perception, signal analysis and decision making. However, these functions can be affected by acquired brain injury (ABI), resulting from traumatic (blows to the head) or non-traumatic factors (tumors, strokes, infections, among others). Annually, about 55 million new cases of ABI are reported, with sequelae that can affect the quality of life of patients and their families. This scenario has driven research into tools to mitigate and recover lost capabilities. The Center for Rehabilitation Engineering and Neuromuscular and Sensory Research (CIRINS) of the Faculty of Engineering of the National University of Entre Ríos in Argentina has developed neuromuscular and sensory rehabilitation systems, with a focus on the innovation of motor rehabilitation tools using EEG-based brain-computer interfaces (BCI). These BCIs stand out for their economy and versatility, showing significant effects in the rehabilitation of motor functions. Challenges in BCI include signal complexity, artifacts, and inter-person variability, making it difficult to estimate user intent and extending calibration time. To mitigate these problems, strategies based on Deep Learning and dictionary learning have been proposed, which allow for sparse representations of data, being robust to noise and missing data, but with challenges in classification. The study proposes to develop a database of electroencephalographic signals applicable in the development of new algorithms for processing and feature extraction of this type of signals, contributing to the development of technology that supports rehabilitation processes.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Entre Ríos
      • Oro Verde, Entre Ríos, Argentina, 3100
        • Faculty of Engineering, National University of Entre Ríos

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Volunteers of legal age and under 60 years of age, of any gender and without a history of neurological diseases

Description

Inclusion Criteria:

  • Willingness and ability to fully understand the purpose and scope of the experiment and to comply with the experiment instructions.
  • Ability to easily distinguish visually the figures in the study.
  • Ability to perform tasks that demand sustained concentration.

Exclusion Criteria:

  • History of neurological diseases.
  • Suffering from any type of musculoskeletal disorder that limits the motor skills necessary for the experiment.
  • Having a significant hearing loss that prevents him/her from hearing the study instructions.
  • Pregnancy.
  • Lack of cooperation.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Healthly Volunteer

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sensory motor rhythms power bands
Time Frame: Day 1
The volunteer performs a movement task after a cue. A 32-channel EEG records signals following the 10-20 system and measures sensory-motor rhythm power bands.
Day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 2, 2024

Primary Completion (Actual)

December 1, 2024

Study Completion (Actual)

December 1, 2024

Study Registration Dates

First Submitted

February 24, 2025

First Submitted That Met QC Criteria

February 28, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 28, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • IS004678

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The study will focus on electroencephalography signals, therefore for now it is not considered relevant to include data from individual participants (IPD).

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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