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.
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