Evaluating agitation in critically ill patients using remote video monitoring

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the effectiveness of a multi-modal evaluation monitoring system for detecting agitation in critically ill patients. Participants who are already receiving this monitoring as part of their standard care will be observed over a period of three years. The study focuses on patients at risk of agitation in the ICU, utilizing remote video and ultra-sensitive detection technology to enhance patient care. The goal is to improve the management of agitation in this vulnerable population.

Why it matters

Who can join: the full rules

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

Where it's running

• the second affiliated hospital, Zhejiang University school of medicine
  Hangzhou, Zhejiang, China Recruiting
• Sahzu
  Hanzhou, Zhejiang, China Active not recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

• Effects of a caregiver's physical contact on ICU patients

  This study tests whether brief physical contact from a patient’s primary caregiver can influence vital signs in adults in intensive care.

  Recruiting Universidad Autonoma del Estado de Mexico · Mexico City, Mexico City · NCT07761364

• How illness severity and death risk relate to breathing and limb muscle strength in ICU patients

  This project will see if how sick ICU patients are and their risk of dying are linked to the strength of their respiratory and skeletal muscles for adults in the ICU.

  Recruiting Istinye University · Istanbul, Esenyurt · NCT07124442

• Immunosuppression and ICU-acquired MDROs in critically ill adults

  This study tests how often ICU patients who are immunocompromised acquire or carry resistant bacteria, and how this relates to infections and outcomes.

  Recruiting University Hospital, Lille · Lille · NCT06652126

• Measuring heart function using AI-guided techniques by minimally trained operators

  This study is testing if a new AI tool can help less experienced staff accurately measure heart function in critically ill ICU patients, so they can better manage their fluid needs.

  Recruiting at 2 sites Assistance Publique - Hôpitaux de Paris · Limoges and 2 other locations · NCT06486467

• Monitoring glucose levels in critically ill patients

  This study looks at how often critically ill patients in the ICU experience low blood sugar and how using continuous glucose monitors can help improve their care.

  Recruiting Universidad Europea de Madrid · Madrid · NCT06234787

• Hepatic Vein Filling Fraction vs TAPSE to Check Right Heart Function in Mechanically Ventilated ICU Patients

  We’re testing if the hepatic vein systolic filling fraction can reliably show how well the right side of the heart is pumping in adults on breathing machines in the ICU.

  Recruiting Menoufia University · Alexandria, Shebin El-Kom · NCT07732114

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.