the Multi-modal Evaluation of Agitation in Critically Ill Patients Based on Remote Video-Ultra-sensitive Detection Wave

A Multi-modal Recognition Model and Efficacy Evaluation for Agitation Behavior in Critically Ill Patients Based on Remote -Ultra-sensitive Detection Wave ---A Multi-center, Open-label, Observational Study

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06543602

Enrollment

580

Registered

2024-08-09

Start date

2024-05-01

Completion date

2027-04-30

Last updated

2024-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critically Ill Patients

Keywords

Critically Ill, agitation, monitoring, remote

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.

Interventions

DIAGNOSTIC_TESTmulti-model monitoring and alert

All agitated critically illed patients are monitored by manual and multi-model monitoring and alert system

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy 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

Design outcomes

Primary

Measure	Time frame
the correct rate for alerting agitated critically ill patients	10-15 seconds every agitated patients during stay in ICU

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026