The ICU-Recover Box: using smart technology for monitoring health status after ICU admission.

The ICU-Recover Box: using smart technology for monitoring health status after ICU admission. - ICU-Recover Box

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON51727

Enrollment

Registered

2022-07-22

Start date

2022-09-26

Completion date

Unknown

Last updated

2026-08-10

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

Conditions

aandoeningen na IC ontslag, het gaat om monitoren van de post IC gezondheidstoestand post ICU monitoring

Interventions

Treatment of subjects on the ICU will be state of the art, conform current practice, protocols and guidelines. Patients discharged from the ICU will receive a ICU-Recover Box on the ward filled wit

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Discharged from ICU after being admitted for at least 24 hours and having received mechanical ventilation.

Exclusion criteria

Exclusion criteria: cardiothoracic patients

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: • 15 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: • 15 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
• 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

• 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

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 25, 2026