Health TrialsbyHealthPanel

ICU-Recover Box 2.0, Smart Technology for Home Monitoring of ICU Patients

ConditionICU Acquired Weakness
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorLeiden University Medical Center

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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).

Disqualifiers

Patient is < 18 years old.

Patient is pregnant.

Patient breastfeeds during the course of the study.

Patient is discharged for palliative care.

Trial design

Design model

Single group

Treatments tested in this trial

  • The ICU-Recover Box: using smart technology for monitoring health status after ICU admission Pilot 2.0

    Device

    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.

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: Patients receiving the ICU-recover box containing home monitoring devicesOther 1 intervention

Trial outcomes

Primary outcomes

1

Use of smart technology

· The percentage of included post-ICU patients that was able to use and actually did use smart technology for twelve consecutive months.

Time frame
12 months
2

Acquisition of data

· That it was possible (y/n) to acquire the data from the remote monitoring and that the investigators were able to store and use the data for analyses

Time frame
12 months

Secondary outcomes

1

Lessons Learnt

That the investigators have an inventory of the lessons learned and feedback from participants, collected by a predefined questionnaire. On a monthly base the investigators will contact participants and ask them: (1) 36 questions on quality of life; (2) 2 questions on health care utilization; and (3) 9 questions on the use of the Corsano equipment. The questions are customised and not part of standardised questionnaires. Some questions are open-ended, while some are scale based (almost never-almost always). The investigators will report the results of these questionnaires qualitatively, as no final "score" can be attributed to the filled out questionnaire.

Time frame
12 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Leiden University Medical Center

Lead sponsor

Source ClinicalTrials.gov
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