RecruitingNCT06289699

Alert Frequency, Nurse, and Patient Satisfaction With a wCVSM Software Across Health Care Systems and Cultures

Alert Frequency, Nurse, and Patient Satisfaction With a Continuous Wireless Vital Sign Monitoring Software Across Health Care Systems and Cultures


Sponsor

Christian S. Meyhoff

Enrollment

100 participants

Start Date

Feb 26, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this prospective, international multi-centre pilot study is to assess the functionality and user experience of a new vital sign monitoring system in 20 patients and 20 nurses in the general ward at each centre. The patients will be monitored with a wireless, continuous vital sign monitoring systems and answer a questionnaire afterwards. They will in addition have vital signs monitored as per standard practice. The nurses will answer a questionnaire after having had the responsibility for a monitored patient for a full shift. The main aims are: To determine the frequency of alerts activated in the app in relation to the alerts that should be activated based on measured data, to explore current practices of in-hospital monitoring by semi-structured interviews to map differences across systems and to test nurse and patient satisfaction.


Eligibility

Min Age: 18 Years

Inclusion Criteria10

  • Adults (≥18 years)
  • Expected stay in the hospital ≥2 days
  • Admitted for surgery with expected duration of surgery \>2 hours or admitted for acute medical condition with at least one of the following vital sign deviations within 24 hours of acute admission, recorded by the staff
  • RR \> 21 breaths pr minute
  • RR \< 11 breaths pr minute
  • Pulse (P) \> 91 beats pr minute
  • Pulse (P) \< 50 beats pr minute
  • SpO2 \< 94 % without oxygen supplementation
  • Systolic BP \< 110 mmHg
  • Systolic BP \> 220 mmHg

Exclusion Criteria4

  • Participant expected not to cooperate with study procedures.
  • Allergy to plaster or silicone.
  • Pacemaker or Implantable Cardioverter Defibrillator (ICD) device.
  • Inability to give informed consent.

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(5)

The Cleveland Clinic Foundation, General Anesthesiology

Cleveland, Ohio, United States

Universitätsklinikum Hamburg-Eppendorf (UKE), Zentrum für Anästhesiologie und Intensivmedizin, Klinik und Poliklinik für Anästhesiologie

Hamburg, Germany

University Medical Center Groningen, Department of Anesthesiology

Groningen, Netherlands

St. Olavs Hospital HF, Klinikk for anestesi og intensivmedisin

Trondheim, Norway

Liverpool University Hospitals NHS Foundation Trust

Liverpool, United Kingdom

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06289699


Related Trials