the Multi-modal Evaluation of Agitation in Critically Ill Patients Based on Remote Video-Ultra-sensitive Detection Wave
Recruiting
- Conditions
- Critically Ill Patients
- Interventions
- Diagnostic Test: multi-model monitoring and alert
- Registration Number
- NCT06543602
- Lead Sponsor
- Second Affiliated Hospital, School of Medicine, Zhejiang University
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 580
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
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description multiple-model monitoring group: agitation monitoring by remote video-radar wave multi-model monitoring and alert -
- Primary Outcome Measures
Name Time Method the correct rate for alerting agitated critically ill patients 10-15 seconds every agitated patients during stay in ICU
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (2)
the second affiliated hospital, Zhejiang University school of medicine
🇨🇳Hangzhou, Zhejiang, China
SAHZU
🇨🇳Hanzhou, Zhejiang, China