About this trial
Important information related to the visual assessment of patients, such as facial expressions, head and extremity movements, posture, and mobility are captured sporadically by overburdened nurses, or are not captured at all. Consequently, these important visual cues, although associated with critical indices such as physical functioning, pain, delirious state, and impending clinical deterioration, often cannot be incorporated into clinical status. The overall objectives of this project are to sense, quantify, and communicate patients' clinical conditions in an autonomous and precise manner, and develop a pervasive intelligent sensing system that combines deep learning algorithms with continuous data from inertial, color, and depth image sensors for autonomous visual assessment of critically ill patients. The central hypothesis is that deep learning models will be superior to existing acuity clinical scores by predicting acuity in a dynamic, precise, and interpretable manner, using autonomous assessment of pain, emotional distress, and physical function, together with clinical and physiologic data.
Eligibility criteria
Qualifiers
aged 18 or older
admitted to UF Health Shands Gainesville ICU ward
expected to remain in ICU ward for at least 24 hours at time of screening
Disqualifiers
under the age of 18
on any contact/isolation precautions
expected to transfer or discharge from the ICU in 24 hours or less
unable to provide self-consent or has no available proxy/LAR
Trial design
Treatments tested in this trial
- Video Monitoring
- Accelerometer Monitoring
- Noise Level Monitoring
- Light Level Monitoring
- Air Quality Monitoring
- EKG Monitoring
- Vitals Monitoring
- Biosample Collection
- Delirium Motor Subtyping Scale 4 (DMSS-4)
Treatment groups
Sponsors and collaborators
University of Florida
Lead sponsor
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborator
National Institute for Biomedical Imaging and Bioengineering (NIBIB)
Collaborator