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Control of Assistive Devices Via Brain-Computer Interface Technology

Control of Assistive Devices Via Brain-Computer Interface Technology

Enrolling By Invitation
All
Phase N/A

Overview

The CONVOY Study is a clinical trial designed to explore the feasibility of participants from the PRIME Study (NCT06429735) using the N1 Implant to control various assistive devices. The main goal is to determine whether participants can successfully modulate their brain activity to control devices, such as an Assistive Robotic Arm (ARA). This study will assess the effectiveness, consistency, and safety of neural control using the ARA and other assistive devices.

Eligibility

Inclusion Criteria:

  • Continued enrollment in the PRIME Study.
  • Implanted with the N1 Implant.

Exclusion Criteria:

  • Explantation or deactivation of the N1 Implant.
  • Insufficient N1 Implant BCI performance demonstrated.
  • Lack of a suitable physical space to perform research sessions.
  • Any condition which, in the opinion of the Investigator, would compromise the candidate's ability to safely participate in the study.

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Study details
    Tetraplegia/Tetraparesis
    Amyotrophic Lateral Sclerosis (ALS)
    Quadriplegia
    Spinal Cord Injury (SCI)
    Spinal Cord Injury Cervical

NCT06710626

Neuralink Corp

9 January 2026

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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