Study of Wearable Wireless Sensors for Early Detection of Patient Deterioration After Major Surgery
Led by University of Edinburgh · Updated on 2026-02-10
1332
Participants Needed
17
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
This research aims to find out if wearable sensors can help detect early signs of health problems after major surgery. The study focuses on surgical patients who might become critically ill after their operations. It evaluates if continuous monitoring of vital signs like heart rate and oxygen levels using wearable devices can identify patient deterioration sooner than standard care. The study is observational and involves multiple countries including Benin, Ghana, Guatemala, India, Mexico, Nigeria, Rwanda, and the United Kingdom.
Participants will wear wireless sensors on their chest and fingers before, during, and after surgery for up to 10 days. These sensors record vital signs continuously but do not affect patient care, as clinical teams will not access the data during the study. The first two stages of the study involved testing device usability with healthcare workers, while this third stage collects real-time sensor and clinical event data to explore links between physiological changes and patient complications.
During the study, participants will have their vital signs monitored with wearable devices while also receiving standard clinical observations. Researchers will collect cardiovascular, respiratory, and temperature data alongside routine care information and clinical events. They will follow patients for 10 days of monitoring plus an additional 30-day follow-up to observe complications. The goal is to gather data to help design future algorithms for early detection of postoperative problems without changing current treatment practices.
CONDITIONS
Brief Title
EMUs: Enhanced Monitoring Using Sensors After Surgery
Research Team
E
Ewen Harrison
E
Eilidh Gunn
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Undergoing elective or emergency major surgery with a planned skin incision of 5 cm or greater
Willing and able to provide written informed consent
You will not qualify if you...
Under 18 years of age
Known or suspected allergy to adhesive dressings
Obstetric patients
Unwilling or unable to provide written informed consent
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Implementation
Duration - Up to 10 days from device application
Participants wear a wireless sensor device before, during, and after their surgery while receiving standard care. Sensor data is collected continuously but not used to make clinical decisions.
Continuous monitoring during hospital stay for up to 10 days
Long-term Monitoring
Duration - 30 days after sensor monitoring ends
Participants are followed up for 30 days after sensor monitoring to assess clinical outcomes and complications.
1 follow-up visit
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Published Research Related To This Trial
Continuous physiological monitoring for the detection of postoperative deterioration: a protocol for a multistage, multicentre, international, prospective cohort study.
Afra Jiwa, Malcolm M Cameron, Adesoji O Ademuyiwa...