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Recruiting NCT05699967

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

Conditions: Deterioration of Patient's State of Health

Sex: All

Ages: 18 Years – N/A

Enrollment: 210

Sponsor: University Hospital, Basel, Switzerland

Location: Switzerland

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.

Eligibility Criteria

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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05699967). StuddyBuddy aggregates publicly available trial information.