NCT03438851

Brief Summary

Symptoms resulting from mild/moderate trauma to the brain are as varied as the individuals who sustain them. The currently held belief is that the majority of healing and functional recovery occurs within the first two years post injury. A large proportion of individuals who sustain mild/moderate brain injuries (mTBIs) do not fully recover, and continue to experience symptoms well beyond two years post injury. Cognitive rehabilitation programs have been shown to be somewhat effective in helping mTBI patients regain some functionality in these executive domains. The purpose of the current study is to use an objective assessment of brain function to track changes during either a full-time or part-time holistic cognitive rehabilitation program, specifically the ABI Wellness (ABIW) program. The NeuroCatch Platform™ test will be used to assess brain functioning before, during and after 3 months in the ABIW program. The NeuroCatch Platform™ test uses electroencephalography (EEG) to measure event-related potential (ERP) signals produced by the brain, in response to an auditory stimulus. Three brain processes are examined with this test: Auditory sensation (ERP marker is the N100), Basic attention (ERP marker is the P300), and Cognitive processing (ERP marker is the N400).

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
7

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2018

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 23, 2018

Completed
28 days until next milestone

First Posted

Study publicly available on registry

February 20, 2018

Completed
15 days until next milestone

Study Start

First participant enrolled

March 7, 2018

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 21, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 21, 2020

Completed
Last Updated

March 18, 2021

Status Verified

March 1, 2021

Enrollment Period

2.1 years

First QC Date

January 23, 2018

Last Update Submit

March 16, 2021

Conditions

Outcome Measures

Primary Outcomes (2)

  • Tracking and comparison of neurophysiological changes (response size) to functional changes as participants complete 3 months of the ABIW program.

    Response size will be measured as amplitude in microvolts. Functional changes will be measured using a proprietary BrainEx Assessment that provides a category score from four cognitive programs of BrainEx.

    3 months

  • Tracking and comparison of neurophysiological changes (response timing) to functional changes as participants complete 3 months of the ABIW program.

    Response timing will be measured as latency in milliseconds. Functional changes will be measured using a proprietary BrainEx Assessment that provides a category score from four cognitive programs of BrainEx.

    3 months

Secondary Outcomes (1)

  • Collection and evaluation of adverse events and adverse device effects

    3 months

Study Arms (2)

Full-time Cognitive Rehabilitation Program

EXPERIMENTAL

Participants in full-time program will be asked to complete 4 experimental sessions with the NeuroCatch Platform™ over the course of 3 months (i.e. one session/ month).

Device: NeuroCatch Platform™

Part-time Cognitive Rehabilitation Program

EXPERIMENTAL

Participants in the part-time program will be asked to complete 3 experimental sessions with the NeuroCatch Platform™ over 3 months (i.e. one session/1.5 months).

Device: NeuroCatch Platform™

Interventions

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.

Full-time Cognitive Rehabilitation ProgramPart-time Cognitive Rehabilitation Program

Eligibility Criteria

Age19 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Enrolled in but not initiated the ABI Wellness program
  • Male or female, 19-65 years old inclusively
  • Normal hearing capabilities
  • Able to understand the informed consent form, study procedures and willing to participate in study
  • Able to keep eyes still for 6 minutes

You may not qualify if:

  • Clinically documented hearing issues (e.g. in-ear hearing problems, punctured ear drum, etc.)
  • Score of 7 or lower on the Mini Mental State Exam (MMSE) - Orientation subscale
  • Implanted pacemaker
  • Metal or plastic implants in skull
  • In-ear hearing aid or cochlear implant, hearing device
  • Recent (within last 6 months) acquired brain injury
  • History of other neurological disorder (e.g. brain cancer, dementia, multiple sclerosis, stroke, etc.)
  • 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
  • Not fluent in English language
  • Unable to provide informed consent
  • Previous participation in studies using the NeuroCatch Platform™
  • If female and of child-bearing potential: pregnant, suspected or planning to become pregnant or breast-feeding
  • History of seizures
  • Allergy to rubbing alcohol or EEG gel

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

HealthTech Connex Inc. Centre for Neurology Studies

Surrey, British Columbia, V3V 0C6, Canada

Location

MeSH Terms

Conditions

Brain Injuries

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System DiseasesCraniocerebral TraumaTrauma, Nervous SystemWounds and Injuries

Study Officials

  • Jan Venter, MBChB MFamMed CCFP IFMCP

    HealthTech Connex Inc. Centre for Neurology Studies

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Participants will self-select into one of two treatment conditions: a full-time intensive program or a part-time program. Participants in the full-time program will be asked to complete 4 experimental sessions with the NeuroCatch PlatformTM over the course of 3 months (i.e. one session/ month); whereas, participants in the part-time program will be asked to complete 3 scans over 3 months (i.e. one session/1.5 months).
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 23, 2018

First Posted

February 20, 2018

Study Start

March 7, 2018

Primary Completion

April 21, 2020

Study Completion

April 21, 2020

Last Updated

March 18, 2021

Record last verified: 2021-03

Locations