the Multi-modal Evaluation of Agitation in Critically Ill Patients Based on Remote Video-Ultra-sensitive Detection Wave
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About
The goal of this observational study is to learn about the effectiveness of the multi-modal evaluation for agitation behavior in critically ill patients based on remote video-Ultra-sensitive detection wave.
The main question it aims to answer is: evaluate the effectiveness of multi-modal evaluation monitoring system for agitated critically ill patients Participants already taking multi-modal evaluation monitoring system as part of their regular medical care for agitated critically ill patients will compare their effectiveness for agitation for 3 years.
Enrollment
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Volunteers
Inclusion criteria
- Patients at risk of agitation in the ICU
- Patients with RASS score -2 and above
- ≦ 65 years old, ≧ 18 years old
Exclusion criteria
- 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
Trial design
580 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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