Observational Study: Wearable Biopatch for Sepsis Readmission

This study is looking at whether a wearable device called BioIntelliSense can help predict if patients who have been hospitalized for sepsis (a serious infection that can lead to organ damage) will need to be readmitted to the hospital within 30 days of going home. We want to see if the information from the biopatch, which monitors things like heart rate and breathing, can improve our ability to predict these readmissions. You may be able to join if you are 18 or older, were diagnosed with sepsis in the emergency department or hospital, and were admitted to the hospital. The study aims to find out if using the biopatch provides useful data to better predict when someone might need to return to the hospital after sepsis.

Study design
This is an observational study involving 200 participants. It is a longitudinal cohort study, meaning participants are followed over time.
What's involved
Participants will wear a BioIntelliSense biopatch on their chest for 30 days after leaving the hospital, or until they are readmitted.
Compensation
Not stated in the trial record.
Follow-up
Participants are followed for 30 days after hospital discharge to check for readmission.

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NCT05806762

Prediction of Rehospitalization Following a Sepsis Admission Using a Wearable Biopatch

Recruiting
Not specifiedAges 18+Observational
University of California, San Diego
~200 participants
Updated 2024-04-03 on ClinicalTrials.gov
What's tested:BioIntellisense

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Hospital readmission
Measured over 30 days
Sepsis
1 sites across 1 states
California1

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  • Hospital readmission30 days

    Patients with an index hospitalization with sepsis will be followed to see if they have an unplanned readmission to the hospital.