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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03421405
Other study ID # NCI_NCClin_001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2, 2018
Est. completion date February 1, 2018

Study information

Verified date March 2021
Source NeuroCatch Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

EEG signals have been collected and studied since the early 1990's as a way of assessing brain function at a gross level. As early as the 1930's a derivative of the raw EEG signal - event-related potentials (ERPs) - have been computed. These scalp-recorded ERPs are the brains response to a stimulus of interest (e.g. a flashing checkerboard or an angry face). The timing and topographical location of ERP components lends insight into the timing and complexity of various cognitive processes. At NeuroCatch Inc., research is primarily focused on three ERP components: the N100, P300 and N400. To elicit the ERP components of interest in this study (N100, P300, N400), proprietary auditory stimulus sequences will be administered using the investigational device, the NeuroCatch Platform™. Each sequence consists of pure tones and word pairs to elicit the various components associated with different attention abilities (sensory processing, target detection & semantic processing). A secondary objective of the study will be to validate the auditory stimulus sequences tested. Understanding the degree to which these neurophysiological components fluctuate over time is crucial to our understanding of typical brain functioning. Research and medicine is moving away from behavioural responses to assess brain health (e.g. verbal responses, reaction time, etc.) and are moving toward more neuroimaging focused measures, such as CT, and MRI scans. The strength of utilizing EEG technology is two-fold: i) it is portable and ii) has high temporal resolution. Looking forward, EEG-based brain assessment technology could be implemented field-side, at the site of an accident for a quick assessment of brain and cognitive functioning, or within a clinicians' office to evaluate treatment efficacy. However, for this type of technology to be useful in quantifying brain health, we must first quantify the degree to which a healthy brain naturally fluctuates in it processing capability. For example, should technology such as the NeuroCatch Platform™ be used as a monitoring tool, we must have an idea of what normal variation is.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date February 1, 2018
Est. primary completion date February 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years to 65 Years
Eligibility Inclusion Criteria: 1. Male or female, 19-65 years old inclusively 2. Normal hearing capabilities 3. Able to understand the informed consent form, study procedures and willing to participate in study 4. Able to keep eyes still for min 6 minutes Exclusion Criteria: 1. Clinically documented hearing issues (e.g. tinnitus, in-ear hearing problems, punctured ear drum, etc.) 2. Implanted pacemaker 3. Metal or plastic implants in skull 4. In-ear hearing aid or chocclear implant, hearing device 5. Chronic neurological disorder (e.g. Stroke, MS, etc.) 6. Recent (within last 6 months) acquired brain injury 7. History of brain cancer 8. History of dementia 9. Exposed to investigational drug or device 30 days prior to start in this study, or concurrent use of investigational drug or device while enrolled in this study 10. Planning to use investigational drugs or devices while enrolled in this study 11. Not fluent in English language 12. Unable to provide informed consent 13. Previous participation in studies using the NeuroCatch Platform™ 14. If female and of child-bearing potential: pregnant, suspected or planning to become pregnant or breast-feeding 15. History of seizures 16. Allergy to rubbing alcohol or EEG gel

Study Design


Related Conditions & MeSH terms


Intervention

Device:
NeuroCatch Platform™
NeuroCatch Platform™ consists of software and hardware that captures brain health information. The platform intends to provide a quick, portable and easy to use solution for the acquisition, display, analysis, storage, reporting and management of electroencephalograph (EEG) and event-related potential (ERP) information.

Locations

Country Name City State
Canada HealthTech Connex Inc. Centre for Neurology Studies Vancouver British Columbia

Sponsors (1)

Lead Sponsor Collaborator
NeuroCatch Inc.

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Variability of response size of selected ERPs (N100, P300, N400) acquired using the NeuroCatch Platform™ during the baseline visit Response size will be measured as amplitude in microvolts. 1 day
Primary Variability of response timing of selected ERPs (N100, P300, N400) acquired using the NeuroCatch Platform™ during the baseline visit Response timing will be measured as latency in milliseconds. 1 day
Secondary Qualitative comparison of ERP graphs generated by different auditory stimulus sequences during the NeuroCatch Platform™ assessment ERP graphs will be overlaid. Trained technician will assess if peaks and valleys occur at expected time points for different sequences. 1 day
Secondary Collection and evaluation of adverse events and adverse device effects Evaluation of safety and tolerability of the NeuroCatch Platform™ device 4 weeks
Secondary Slope of change over time in response size to quantify the natural variability in selected ERPs (N100, P300, N400) acquired using NeuroCatch Platform™ Response size will be measured as amplitude in microvolts. Means will be calculated and compared over time. 4 weeks
Secondary Slope of change over time in response timing to quantify the natural variability in selected ERPs (N100, P300, N400) acquired using NeuroCatch Platform™ Response timing will be measured as latency in milliseconds. Means will be calculated and compared over time. 4 weeks
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