- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06861517
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
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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.
Sponsor
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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