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Continuous Vital Sign Monitoring in a Surgical Ward

StatusRecruiting
PhaseNot specified
Started
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Record status
This record was last updated July 9, 2026 (before its estimated October 1, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Eligibility criteria shortened, about 21 words Secondary endpoints: details revised at 2 of 5 entriesv2 Show 1 more changeShow less
    • Secondary endpoints: details revised at 2 of 5 entries

    See this version in full on ClinicalTrials.gov ↗

  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Unsafe patient care remains a major contributor to global morbidity and mortality. In surgical wards, postoperative patients are typically monitored intermittently using the National Early Warning Score (NEWS-2), leaving periods during which clinical deterioration may go undetected. Continuous vital sign monitoring (CVSM) using wearable sensors offers the potential for earlier identification of deterioration compared with intermittent assessments. CVSM was introduced in a hospital ward as part of a hospital-initiated pilot implementation and is used alongside standard monitoring with NEWS-2. The purpose of the study is to evaluate this implementation. This observational study uses a pragmatic, quasi-experimental, multi-method, longitudinal design. The overall aims of the study are to evaluate the impact of CVSM implementation on patient outcomes, to explore healthcare professionals' perceptions of patient safety culture, turnover intention and pleasure of work, and to describe their experiences with implementation.
Trial Details
NCT Number NCT07690267
Lead Sponsor University Hospital, Akershus
Collaborators: Norwegian University of Science and Technology
Conditions Patient Monitoring, Wearable Devices, Telemonitoring, Patient Safety, Patient Deterioration, Nurses, Healthcare Professionals, Work-related Outcomes +2 more
Enrollment 9,600 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov