NCT06543602 · RECRUITING
the Multi-modal Evaluation of Agitation in Critically Ill Patients Based on Remote Video-Ultra-sensitive Detection Wave
This observational study is testing a monitoring system that uses remote video and ultra-sensitive motion-detection technology to identify agitation in critically ill ICU patients. Researchers want to know how well this multi-modal system works compared to standard assessment methods. There is no assigned phase listed, and no drug or therapy is being given — this is purely a diagnostic and monitoring technology study conducted over three years.
You may qualify if
- Patients at risk of agitation in the ICU
- Patients with RASS score -2 and above
- ≦ 65 years old, ≧ 18 years old
You're excluded if
- The affected party refused to participate in this study
- Missing/incomplete information
- Vulnerable groups such as pregnant women, those who lack the capacity for civil conduct and do not have the consent of their legal representatives
- Maxillofacial trauma, burns, tumors, surgery, etc. affect facial expression
- Patients with limb impairment and amputation
- Spinal cord injury, limb movement/sensory limitations
- Patients with pre-existing neurological/psychiatric diseases
- Patients with malignant tumors
- Patients with infectious diseases
- Patients with terminal disease and dying disease
- Abnormal behavior due to head injury or craniocerebral disease
The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.
Eligibility criteria as of 2024-08-09