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The ICU-recover Box, Using Smart Technology for Monitoring Health Status After ICU Admission

NCT05766319 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2024-06-14

No results posted yet for this study

Summary

In this pilot study we will study the feasibility of providing and following ICU patients with smart technology for three months after discharge from a general ward of the Leiden University Medical Centre.

Conditions

  • Critically Ill
  • ICU Survivor
  • User Experience

Interventions

DEVICE

Withings ScanWatch

Withings ScanWatch, from which the following features will be used: * Measurement of peripheral oxygen saturation (%) * Automatic recording of heart rate (beats/min) * Automatic recording of activity (step count) (numbers/day)

DEVICE

Withings BPM Connect

Withings BPM connect, from which the following feature will be used: o Measurement of non invasive bloodpressure (mmHg)

DEVICE

Withings Body

Withings Body (Scale), from which the following feature will be used: o Measurement of body weight (kg)

Sponsors & Collaborators

  • Leiden University Medical Center

    lead OTHER

Principal Investigators

  • Sesmu Arbous, MD PhD · LUMC

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-26
Primary Completion
2024-05-31
Completion
2024-05-31

Countries

  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05766319 on ClinicalTrials.gov