Skip to main content
Clinical Trials/NCT06521736
NCT06521736
Enrolling By Invitation
Not Applicable

Compatibility Between Brain-Computer Interface and High Efficiency Augmentative and Alternative Communication Systems: Commercial Readiness

Kendrea Garand1 site in 1 country40 target enrollmentSeptember 13, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-Verbal Communication
Sponsor
Kendrea Garand
Enrollment
40
Locations
1
Primary Endpoint
Commercial readiness of augmentative and alternative communication brain-computer interface (AAC-BCI) system.
Status
Enrolling By Invitation
Last Updated
7 months ago

Overview

Brief Summary

The goal of this clinical trial is to evaluate the commercial readiness of an Augmentative and Alternative Communication Brain-Computer Interface (AAC-BCI) device for people with minimal movement who benefit from expressive communication technology. Our clinical trial focuses on up to 8 AAC-BCI users but involves a team of support participants with different roles: an industry partner's consultant, a speech language pathologist (SLP), and the user's in-home support person. Patient and team reported outcome measures data will be collected on usage, performance, reliability and comfort along with performance data of using the AAC-BCI device in the home.

Detailed Description

Our clinical trial focuses on 8 Alternative Communication Brain-Computer Interface (AAC-BCI) users but involves a team of support participants with different roles: an industry partner's consultant, a speech language pathologist (SLP) and the user's in-home support person. The AAC-BCI user and support person will be recruited from the SLP's clinic and screened to confirm that the individuals meet the inclusion and exclusion criteria before enrollment. The investigators intend to recruit users with a perceived need for Brain-Computer Interface (BCI) access, ex: eye gaze access is deteriorating, unable to determine another access method. The investigators expect that our user participants will be in late-stage amyotrophic lateral sclerosis (ALS), diagnosed with a brainstem stroke, other degenerative neurologic disorder such as Kennedy disease, or have severe quadriplegic cerebral palsy. The support person will be screened to ensure they are comfortable with technology, learning innovative technology and are available to set-up the AAC-BCI daily at the user's request. The home must have internet. A total of 8 enrolled users means that the investigators will have up to 16 team members supported by a consultant. All clinical trial activity will occur in the home. Once consented and enrolled, the first training session with set-up and calibration will occur with the SLP and PRC consultant. The support person must be present. A second training session with a calibration check and use and training on electroencephalogram (EEG) and logfile data collection will occur within one week. The following baseline data will be collected by the consultant and SLP: 1) A functional rating scale; 2) copy spell task (15 minutes); 3) free spell task (15 minutes); National Aeronautics and Space Administration (NASA) Task Load Index (TLX). The roles of the team members are as follows: * Industry partner's consultant: Participate in initial and follow-up AAC-BCI training sessions, provide technology support as needed via phone call, virtual meeting, or home visit. Complete required inventory and data forms. Conduct monthly home visits. * Speech Language Pathologist (SLP): Participate in initial and follow-up AAC-BCI training sessions. Provide treatment and standard of clinical care as needed via phone call, virtual meeting, or home visit. Complete required data forms related to clinical care and support. Complete inventory and data forms. * AAC-BCI User: Participate in initial set-up, calibration, and training sessions. Use at home at least 10 hours a week with EEG activity. Use system for daily communication during time they are wearing it. Participate in monthly home visit with SLP and weekly follow-up call with researcher to collect data. Complete surveys on effectiveness when trying to communicate and effectiveness when not trying to communicate. * Support Person: Participate in initial set-up, calibration, and training sessions. Agree to set-up for AAC-BCI user in the home so that the user is wearing the headgear, and the EEG electrodes are active for at least 10 hours a week. Complete recommended cleaning and storage of equipment after use. Participate at monthly visits with consultant, contacts with the SLP and weekly call with researchers. Complete data collection forms. At the end of the 6-month study, participants will complete a Qualtrics survey to rate the overall commercial readiness of the AAC-BCI device along with rating the AAC-BCI device on satisfaction, performance, reliability, and comfort.

Registry
clinicaltrials.gov
Start Date
September 13, 2024
End Date
April 30, 2026
Last Updated
7 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Kendrea Garand
Responsible Party
Sponsor Investigator
Principal Investigator

Kendrea Garand

Associate Professor

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • For augmentative and alternative communication, brain-computer interface (AAC-BCI) Users:
  • Natural speech does not meet daily communication needs requiring the use of a speech generating device
  • Receiving speech therapy from a licensed speech language pathologist
  • Has been assessed for and currently using a speech generating device as a means of communication
  • Has a diagnosis resulting in minimal movement interfering with direct selection to a keyboard or AAC display
  • Has a support person who is comfortable with technology, willing to learn a new technology system and is available to set-up the AAC-BCI daily at the user's request.
  • In-home internet access
  • Environment that is suitable for setting up the in-home AAC-BCI system
  • Individuals aged 14 or older
  • Speaks English

Exclusion Criteria

  • For AAC-BCI Users:
  • Does not own or use a speech generating device
  • Unable to participate during the scheduled time periods
  • History of photosensitive epilepsy
  • History of uncorrectable hearing loss
  • Unable to participate during scheduled times
  • Has a history of open scores on the scalp
  • Does not speak English
  • For Support Persons:
  • Unable to participate during the scheduled time periods

Outcomes

Primary Outcomes

Commercial readiness of augmentative and alternative communication brain-computer interface (AAC-BCI) system.

Time Frame: 6 months

Stakeholder participants agree "yes" that the Alternative Communication Brain-Computer Interface (AAC-BCI) system is ready for product release with an average combined agreement of 70% on a binary yes/no scale.

Secondary Outcomes

  • Alternative Communication Brain-Computer Interface (AAC-BCI) system comfort(6 months)
  • Alternative Communication Brain-Computer Interface (AAC-BCI) system user-satisfaction(6 months)
  • Alternative Communication Brain-Computer Interface (AAC-BCI) system performance(6 months)
  • Alternative Communication Brain-Computer Interface (AAC-BCI) system reliability(6 months)

Study Sites (1)

Loading locations...

Similar Trials