SeeMe: Using Automated Facial Tracking to Detect Voluntary Behavior in Brain Injury

Recruiting N/A Interventional Study
Traumatic Brain Injury (TBI) Patients Severe Traumatic Brain Injury
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
22 – 85
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
80 (estimated)
Sponsor
Stony Brook University · Other
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About This Trial
Objective: This prospective interventional study introduces "SeeMe," an automated, high-resolution computer vision platform designed to objectively quantify microscopic, auditory command-evoked movements in patients with Traumatic Brain Injury (TBI). Current clinical assessments, such as the Glasgow Coma Scale (GCS) and Coma Recovery Scale-Revised (CRS-R), rely on subjective human observation and …
Trial Locations
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Eligibility Criteria
Group 1: Traumatic Brain Injury (TBI) Cohort Inclusion Criteria: * Adults (22+) with a history of acute traumatic brain injury * Documented loss of consciousness with a Glasgow Coma Scale (GCS) score less than or equal to 8 upon hospitalization * Clinically stable as determined by the primary neur…
Contacts

Sima Mofakham, PhD

631-444-1278

sima.mofakham@stonybrookmedicine.edu

CONTACT