CompletedNot Applicable

Development of an Automatically Generated and Wearable-based Early Warning System

Switzerland210 participantsStarted 2023-02-07

Plain-language summary

The aim of this project is to create an automated EWS and analyze whether the use of wearable devices is suitable for vital sign measurements in a hospital by using the recording of vital parameters taken by nurses via the Clinical Information System (HIS) combining them with vital sign measurements coming from wearable devices.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Planned hospital stay \> 24 hours * Written informed consent as documented by signature from the participant Exclusion Criteria: * Unable or not willing to sign informed consent * Wearable cannot be worn due to comprehensible reasons (allergic reactions, wounds, amputations, excessive hairiness, edema, venous access, other) * Significant mental or cognitive impairment

What they're measuring

Number of correctly automatically calculated scores

Timeframe: one time assessment at Day 1

Trial details

NCT IDNCT05699967

SponsorUniversity Hospital, Basel, Switzerland

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2023-09-14

View on ClinicalTrials.gov More Deterioration of Patient's State of Health trials