Study Stopped
NeuroCatch Platform became commercially available (Health Canada License approved) and can now be incorporated into the ABI Wellness Program
Assessing Brain Changes Throughout the ABI Wellness Program
Assessing Neurophysiological Changes in Individuals With Chronic Traumatic Brain Injury Symptoms Throughout a Full-time or Part-time Holistic Cognitive Rehabilitation Program: An Initial Assessment.
1 other identifier
interventional
7
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2018
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 23, 2018
CompletedFirst Posted
Study publicly available on registry
February 20, 2018
CompletedStudy Start
First participant enrolled
March 7, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 21, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
April 21, 2020
CompletedMarch 18, 2021
March 1, 2021
2.1 years
January 23, 2018
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
EXPERIMENTALParticipants 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).
Part-time Cognitive Rehabilitation Program
EXPERIMENTALParticipants 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).
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.
Eligibility Criteria
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
- NeuroCatch Inc.lead
Study Sites (1)
HealthTech Connex Inc. Centre for Neurology Studies
Surrey, British Columbia, V3V 0C6, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jan Venter, MBChB MFamMed CCFP IFMCP
HealthTech Connex Inc. Centre for Neurology Studies
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- 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