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

The ICU-Recover Box: using smart technology for monitoring health status after ICU admission Pilot study 2.0 - Using smart devices to monitor patients recovery post-ICU admission.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON57282

Enrollment

Registered

2024-02-27

Start date

2025-01-01

Completion date

Unknown

Last updated

2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical, cognitive and mental impairment. ICU-related physical and mental impairment

Interventions

None listed

Eligibility

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Discharged from ICU.

Exclusion criteria

Exclusion criteria: ICU admission shorter than 24 hours. Not intubated and ventilated.

Design outcomes

Primary

Measure	Time frame
Primary endpoint of this study is the feasibility of providing patients with the ICU-Recover Box after ICU discharge and before hospital discharge, including the collection of measurement/questionnaire data after hospital discharge. This study will be used to identify the issues when implementing such a system. Feasibility is defined as: • 50 post-ICU patients, who gave informed consent and who were discharged from hospital with the ICU-Recover Box, were able to use the devices within its intended use. • We were able to acquire data from the devices in the ICU-Recover Box. • We were able to store the acquired data in a safe manner. • We were able to analyse the acquired data. • > 80 % of the persons that were discharged with an ICU-Recover Box contributed for 3 months to post-ICU data.	—

Measure

Time frame

Primary endpoint of this study is the feasibility of providing patients with the ICU-Recover Box after ICU discharge and before hospital discharge, including the collection of measurement/questionnaire data after hospital discharge. This study will be used to identify the issues when implementing such a system. Feasibility is defined as: • 50 post-ICU patients, who gave informed consent and who were discharged from hospital with the ICU-Recover Box, were able to use the devices within its intended use. • We were able to acquire data from the devices in the ICU-Recover Box. • We were able to store the acquired data in a safe manner. • We were able to analyse the acquired data. • > 80 % of the persons that were discharged with an ICU-Recover Box contributed for 3 months to post-ICU data.

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Secondary

Measure	Time frame
Secundary study parameters/outcome of the study (if applicable): • Users, i.e. post-ICU patients, have been asked, by short interviews, for feedback and suggested adjustments and improvements of the ICU-Recover Box. And when deemed relevant, adjustments and improvements to the ICU-Recover Box or procedures for adequate use will be made. • By means of PDCA cycli, the lessons learned and feedback will have led to adjustment and improvement of the ICU-Recover Box, from its content and its use to data acquisition and data analysis.	—

Measure

Time frame

Secundary study parameters/outcome of the study (if applicable): • Users, i.e. post-ICU patients, have been asked, by short interviews, for feedback and suggested adjustments and improvements of the ICU-Recover Box. And when deemed relevant, adjustments and improvements to the ICU-Recover Box or procedures for adequate use will be made. • By means of PDCA cycli, the lessons learned and feedback will have led to adjustment and improvement of the ICU-Recover Box, from it*s content and it*s use to data acquisition and data analysis.

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Countries

Netherlands

Contacts

Public ContactJ.D. Hemel-Rintjap

Leids Universitair Medisch Centrum

j.d.van_hemel-rintjap@lumc.nl071-5265018

Outcome results