Actively Recruiting
ICU-Recover Box 2.0, Smart Technology for Home Monitoring of ICU Patients
Led by Leiden University Medical Center · Updated on 2025-09-29
50
Participants Needed
1
Research Sites
74 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
ICU-Recover Box 2.0, Smart Technology for Home Monitoring of ICU Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Leiden University Medical Center
Leiden, South Holland, Netherlands, 2333 ZA
Actively Recruiting
Research Team
S
Sesmu Arbous, MD PhD
CONTACT
T
Tina van Hemel-Rintjap, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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