ICU-Recover Box 2.0, Smart Technology for Home Monitoring of ICU Patients
The ICU-Recover Box: Using Smart Technology for Monitoring Health Status After ICU Admission Pilot Study 2.0
Leiden University Medical Center
50 participants
Jul 1, 2025
INTERVENTIONAL
Conditions
Summary
Smart technology could improve quality of care in patients who have been admitted to the ICU and have been discharged from ICU and hospital, by early diagnosis of complications and early (ambulatory) treatment. With the ICU-Recover Box and its smart technology the investigators see new opportunities to improve patient health and to recognize early if escalation of medical care is needed. The primary objective of the pilot study is to assess the feasibility of the use of smart technology by persons that have been discharged from the ICU in the twelve months following ICU discharge.
Eligibility
Inclusion Criteria6
- Patient has been admitted to the ICU of the LUMC for > 24 hours.
- Patient has received mechanical ventilation.
- Patient masters the English or Dutch language.
- Patient is able to use smart technology at home. (i.e. Wi-Fi available, sufficient comprehension of smart technology).
- Patient can be contacted and informed about the ICU-Recover box on one of the clinical wards of the LUMC.
- Patient is discharged from a ward within the LUMC to home or an extra-hospital facility.
Exclusion Criteria7
- Patient is < 18 years old.
- Patient is pregnant.
- Patient breastfeeds during the course of the study.
- Patient is discharged for palliative care.
- Patient is considered an incapacitated adult.
- Patient is unwilling to sign the informed consent form.
- Patient is discharged to another hospital.
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Interventions
The Corsano CardioWatch 287-2 measures blood pressure, heart rate, heart rate variability, respiratory rate, peripheral oxygen saturation, body temperature and their daily activity.This devices is used for personal management, never to directly base a diagnosis or treatment on. The patient has to download the Corsano App on his/her mobile phone.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07162948