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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

580 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-05-01

Study Completion Date

2027-04-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Critically Ill Patients

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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control group: monitoring by manual way

No interventions assigned to this group

multiple-model monitoring group: agitation monitoring by remote video-radar wave

multi-model monitoring and alert

Intervention Type DIAGNOSTIC_TEST

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

Interventions

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multi-model monitoring and alert

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

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No