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NCP 2.0 Repeat Study

Assessing Repeatability of the NeuroCatch Platform 2.0 Stimulus Sequences

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04661592
Enrollment
36
Registered
2020-12-10
Start date
2020-11-30
Completion date
2021-08-31
Last updated
2022-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Health

Brief summary

The NeuroCatch Platform™ version 2.0 (NCP2.0), an investigational medical device system developed by NeuroCatch Inc., 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; brain response to a stimulus) information. The purpose of the study is to understand how reliable and repeatable the ERP metrics elicited by the NCP platform are within participants over multiple sessions.

Detailed description

A new method for creating stimulus sequences was developed for NeuroCatch™ Platform 2.0. Rather than using a set of fixed, predetermined sequences to elicit ERPs this new method draws on a database of candidate word stimuli to generate a different, random stimulus sequence each time a scan is carried out. The goal of this is to reduce habituation to the stimulus sequences which is hypothesized to improve the repeatability of the component measurements. Characterizing how individuals respond to the stimulus sequences is an important step in the validation of the generation method itself. Understanding the degree of variability and prototypical values of each ERP component is crucial to the understanding of typical brain functioning. For this type of technology to be clinically viable in quantifying brain health, the investigators must first quantify the degree to which a healthy brain naturally fluctuates in it processing capability. This study is being carried out to assess how repeatable the ERPs elicited by the new method are while also considering the impact of intraindividual variability observed in previous investigations. Thus, by comparing the results of the scans over time, an assessment of the reliability of the new stimulus sequences can be made.

Interventions

DEVICENeuroCatch Platform

To elicit the ERP components of interest in this study (N100, P300, N400), proprietary auditory stimulus sequences will be administered using the NeuroCatch™ Platform version 2.0, an investigational medical device. Each sequence consists of tones and word pairs to elicit the various components of interest. Version 2.0 of the NeuroCatch™ Platform consists of a computerized acquisition software which presents the stimulus, acquires the data and presents the amplitude and latency values of the ERP components (N100, N400, P300)

Sponsors

NeuroCatch Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

Longitudinal

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Any sex, at least 19 years of age or older 2. Able to understand the informed consent form, study procedures and willing to participate in study 3. Able to remain seated and focused for 7 minutes 4. In good health with no history of clinically relevant neurological illness or injury in the last 5 years

Exclusion criteria

1. Requires the use of hearing aids or a cochlear implant, diagnosed with tinnitus that is currently active, or has temporary damage to earing (e.g. punctured ear drum). Or unable to detect a 740Hz tone played at 85dB in both ears. 2. Implanted pacemaker or implanted electrical stimulators 3. Metal or plastic implants in the skull, excluding dental/facial implants 4. Exposed to an investigational drug or device 30 days prior to start in this study, or concurrent or planned use of investigational drug or device while enrolled in this study 5. Not proficient in English language 6. Diagnosed epilepsy or history of seizures 7. If female and of child-bearing potential: pregnant, suspected or planning to become pregnant or breast-feeding 8. Unhealthy scalp (apparent open wounds and/or bruised or weakened skin)

Design outcomes

Primary

MeasureTime frameDescription
Change in Latency of the N400 ERP acquired using the NeuroCatch™ Platform over 2 weeks - variabilityBaseline, +1 Week, +2 WeeksLatency (response speed) will be measured in milliseconds. The statistic being used to measure the variability over three time points will be the group-mean of the individual standard deviations of the measures over the three time points
Change in amplitudes of the N400 ERP acquired using the NeuroCatch™ Platform over 2 weeks - repeatabilityBaseline, +1 Week, +2 WeeksAmplitude (response size) will be measured in microvolts. The statistic being used to measure the repeatability over three time points will be the intraclass correlation coefficient (ICC). Specifically, the two-way mixed single measures absolute agreement type of ICC (denoted as ICC(A,1)) will be used in this analysis.
Change in amplitudes of the N400 ERP acquired using the NeuroCatch™ Platform over 2 weeks - variabilityBaseline, +1 Week, +2 WeeksAmplitude (response size) will be measured in microvolts. The statistic being used to measure the variability over three time points will be the group-mean of the individual standard deviations of the measures over the three time points
Change in Latency of the N400 ERP acquired using the NeuroCatch™ Platform over 2 weeks - repeatabilityBaseline, +1 Week, +2 WeeksLatency (response speed) will be measured in milliseconds. The statistic being used to measure the repeatability over three time points will be the intraclass correlation coefficient (ICC). Specifically, the two-way mixed single measures absolute agreement type of ICC (denoted as ICC(A,1)) will be used in this analysis.
Change in amplitudes of the N100 ERP acquired using the NeuroCatch™ Platform over 2 weeks - repeatabilityBaseline, +1 Week, +2 WeeksAmplitude (response size) will be measured in microvolts. The statistic being used to measure the repeatability over three time points will be the intraclass correlation coefficient (ICC). Specifically, the two-way mixed single measures absolute agreement type of ICC (denoted as ICC(A,1)) will be used in this analysis.
Change in amplitudes of the N100 ERP acquired using the NeuroCatch™ Platform over 2 weeks - variabilityBaseline, +1 Week, +2 WeeksAmplitude (response size) will be measured in microvolts. The statistic being used to measure the variability over three time points will be the group-mean of the individual standard deviations of the measures over the three time points
Change in Latency of the N100 ERP acquired using the NeuroCatch™ Platform over 2 weeks - repeatabilityBaseline, +1 Week, +2 WeeksLatency (response speed) will be measured in milliseconds. The statistic being used to measure the repeatability over three time points will be the intraclass correlation coefficient (ICC). Specifically, the two-way mixed single measures absolute agreement type of ICC (denoted as ICC(A,1)) will be used in this analysis.
Change in Latency of the N100 ERP acquired using the NeuroCatch™ Platform over 2 weeks - variabilityBaseline, +1 Week, +2 WeeksLatency (response speed) will be measured in milliseconds. The statistic being used to measure the variability over three time points will be the group-mean of the individual standard deviations of the measures over the three time points
Change in amplitudes of the P300 ERP acquired using the NeuroCatch™ Platform over 2 weeks - repeatabilityBaseline, +1 Week, +2 WeeksAmplitude (response size) will be measured in microvolts. The statistic being used to measure the repeatability over three time points will be the intraclass correlation coefficient (ICC). Specifically, the two-way mixed single measures absolute agreement type of ICC (denoted as ICC(A,1)) will be used in this analysis.
Change in amplitudes of the P300 ERP acquired using the NeuroCatch™ Platform over 2 weeks - variabilityBaseline, +1 Week, +2 WeeksAmplitude (response size) will be measured in microvolts. The statistic being used to measure the variability over three time points will be the group-mean of the individual standard deviations of the measures over the three time points
Change in Latency of the P300 ERP acquired using the NeuroCatch™ Platform over 2 weeks - repeatabilityBaseline, +1 Week, +2 WeeksLatency (response speed) will be measured in milliseconds. The statistic being used to measure the repeatability over three time points will be the intraclass correlation coefficient (ICC). Specifically, the two-way mixed single measures absolute agreement type of ICC (denoted as ICC(A,1)) will be used in this analysis.
Change in Latency of the P300 ERP acquired using the NeuroCatch™ Platform over 2 weeks - variabilityBaseline, +1 Week, +2 WeeksLatency (response speed) will be measured in milliseconds. The statistic being used to measure the variability over three time points will be the group-mean of the individual standard deviations of the measures over the three time points

Secondary

MeasureTime frameDescription
Change in hours of sleep of the day of scanBaseline, +1 Week, +2 WeeksSecondary statistical analyses will explore the correlation between hours of sleep on the day of scan with changes in ERP measures (primary outcomes) across the sample
Change in perceived mood on the day of scanBaseline, +1 Week, +2 WeeksSecondary statistical analyses will explore the correlation between perceived mood (ranked on a scale of 0-100) on the day of scan with changes in ERP measures (primary outcomes) across the sample
Collection and evaluation of adverse events and adverse device effectsAt time of eventEvaluation of safety and tolerability of the NeuroCatch™ Platform device

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026