
The second VOICE trial participant, Kenneth Shock, whose 𝕏 handle is @Cyborg21, received his implant at UT Southwestern in Dallas, Texas. According to his 𝕏 bio, he is originally from Spokane, Washington, and now residing in Alberta, Canada. Shock is a former medical professional diagnosed with upper motor neuron dominant ALS in 2023, though he suspects symptoms began 10 to 15 years earlier.
ALS has gradually taken away Kenneth’s ability to speak. Through Neuralink’s VOICE clinical trial, he’s exploring how a brain-computer interface designed to translate thought to speech could help restore autonomy in his daily life.
— Neuralink (@neuralink) March 24, 2026
Watch to learn more: pic.twitter.com/C9QufqhI6R
As a graduate of the ALS Canada CALI 2025 program, he has expressed strong enthusiasm for the technology, stating, "ALS is a ruthless, soul-crushing bastard that kicks you when you're down, but @Neuralink? That's the middle finger we're finally flipping back at it."
One early example of related functionality is seen in participant Brad, who uses his implant for text-to-speech, though VOICE advances this by bypassing intermediaries like keyboards. The FDA granted Breakthrough Device Designation for this speech restoration technology in mid-2025, expediting its development. This trial builds on Neuralink's CONVOY study, which explores control of robotic arms, showing the company's layered approach to restoring autonomy.
Neuralink has made significant strides in its human trials, reaching at least 21 successful implants by January 2026. The company began its PRIME study in 2024, focusing on individuals with quadriplegia from spinal cord injuries or ALS. Initial implants started with a small number of participants, but the pace accelerated throughout 2025. With ongoing procedures in early 2026, the total has reached at least 27, incorporating international sites in Canada and the UK. These implants involve the Telepathy device, which uses 1,024 electrodes on ultra-thin threads (64 threads in early implants and 128 in later ones) to record neural signals, enabling users to interact with computers and control assistive robotic arms.
Got a good question from a viewer about Neuralink's VOICE trial:
— Neura Pod – Neuralink (@NeuraPod) January 19, 2026
"How was this Breakthrough Device Designation different from what is implanted in P3 (Brad @ALScyborg) who uses his implant for communication?"
Brad's Neuralink is not implanted in his speech motor cortex.… https://t.co/ef2EDWn0WK
The VOICE trial represents a specialized branch of Neuralink's research, aimed at translating thoughts directly into speech for those with severe speech impairments. Unlike earlier implants focused on cursor control or basic communication via on-screen keyboards, VOICE targets the speech motor cortex to produce voice output directly. As of January 2026, at least two patients have been implanted under this trial, marking an important step toward broader applications.
The trial, officially titled "VOICE: An Early Feasibility Study of a Precise Robotically Implanted Brain-Computer Interface for Communication Restoration," is recruiting participants and focuses on adults aged 22 to 75 with severe speech impairment and impaired upper limb function due to conditions like ALS, primary lateral sclerosis, stroke, or spinal cord injury. It requires participants to have a life expectancy of at least 12 months, the ability to communicate in English, and a stable caregiver. The study excludes those with high risks for surgery, such as morbid obesity, uncontrolled seizures, or certain psychiatric disorders.

Conducted at The University of Texas Southwestern Medical Center in Dallas, Texas, the trial started on October 3, 2025, with an estimated enrollment of six participants and primary completion expected in October 2028. The interventions include the N1 Implant, a skull-mounted wireless rechargeable device connected to electrode threads, and the R1 Robot for precise implantation.
Primary outcomes measure the proportion of device-related and procedure-related adverse events at 12 months, while secondary outcomes track long-term safety up to 48 months and efficacy through metrics like electrode insertion success and words per minute in brain-computer interface performance for speech.
We've received Breakthrough Device Designation from the FDA to help restore communication for individuals with severe speech impairment. (1/3) pic.twitter.com/ou5hQoUtvp
— Neuralink (@neuralink) May 1, 2025
Patients with Neuralink implants report improved quality of life through enhanced interaction with technology. For instance, participants have streamed over 50,000 hours of neural data (Neuralink, October 2026), playing games, browsing the internet, and controlling cursors. In the VOICE trial, the two individuals implanted by January 2026 are exploring direct thought-to-voice capabilities, which could allow faster communication compared to traditional assistive devices.
The 27+ participants include people with spinal cord injury and ALS, with implants providing data on long-term stability and efficacy. Neuralink's upgrades, such as doubling threads to 128 and reducing insertion time to about 1.5 seconds per thread, have addressed early issues like thread retraction, leading to better performance.
Neuralink's growth includes international trials and automated surgical advancements. Elon Musk announced plans for high-volume production and fully automated procedures by late 2026, aiming for thousands of implants annually. The company raised $650 million in 2025, valuing it at around $9 billion, to support this scaling.
Future milestones include the Blindsight implant for vision restoration. Neuralink said Blindsight trials would start in 2026; as of October 2026 no Blindsight trial has launched. With patients around the world logging double-digit hours of use daily, Neuralink is preparing for FDA approvals and wider accessibility.