The EYE-SYNC technology is a Virtual Reality (VR) based digital health platform that can assess real time brain health, deliver therapy, and improve performance. It provides a battery of assessments that can be used to rapidly detect concussion and other cognitive impairments. Once these impairments are identified, trained clinicians can use various paradigms for monitoring improvement over time or to provide therapy to improve visual and vestibular function.

EYE-SYNC is the proprietary analysis metrics used to quantify and objectively determine a patient’s real time cognitive performance. Developed over a 15-year period of rigorous scientific research in collaboration with the US Department of Defense and the Brain Trauma Foundation, EYE-SYNC’s clinical utility has been extensively documented in dozens of publications. In 2016, the FDA cleared EYE-SYNC for viewing, recording, and analyzing eye movements in support of visual impairment identification. In 2019, the FDA selected EYE-SYNC as Breakthrough Device Designation for aid to concussion assessment. In 2021, the FDA cleared EYE-SYNC as an aid to concussion diagnosis.

EYE-SYNC has been shown to increase patient volume, improve the quality of clinical care, and increase revenue for both clinicians and financial decision makers. With established reimbursement, organizations can quickly capture ROI and drive growth. Contact us to learn more about how we can help develop and promote the use of EYE-SYNC in your clinic.

Absolutely. The EYE-SYNC technology is a complimentary diagnostic and therapeutic tool that can be used in conjunction with most commonly used neurocognitive assessments available today.

Each eye tracking assessment is less than 60 seconds in length, creating a mechanism for rapid screening and identification. This approach to rapid testing has been shown to improve both clinical workflow and patient throughput.

No. In certain situations, we recommend a baseline to better understand individual performance differences over time, however it is not necessary. Results can be definitely determined with a positive or negative indication of concussion, or compared against de-identified normative results directly from our clinical trial database.

The results are generated instantaneously following the completion of each assessment. They are provided in a robust advanced report that can be customized to your preferences. Results can also be exported via PDF or secure data transfer to an EMR or other database through our API.

For detailed pricing information, please contact us directly and a live sales representative will contact you directly.

Each purchase includes a fully integrated VR headset, an Android tablet, a durable carrying case for portable use, and various accessories to clean and manage the hardware properly.

All users are formally trained on the EYE-SYNC technology. We provide this service, on most occasions, in person and at the site of your clinical care environment. As an alternative, live video trainings can be arranged however are not recommended.

Most clinicians can become certified users of the EYE-SYNC technology, upon completion of the in person training,

In addition to your hardware/software purchase, we provide real time clinical and technical support as often as you need it. Our clinical experts can help support test administration workflows, protocol design, and result interpretation. We also provide unlimited access to the SyncThink Knowledge Base where you can access information on our research, products, and materials as you need them.

If interested in a trial period to further evaluate the EYE-SYNC technology, please contact us directly.

The battery of eye tracking assessments cannot be performed in patients who experience complete vision loss without glasses or hard contacts, since we require removal of these lenses during testing.