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

NCT06289699 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2025-08-12

No results posted yet for this study

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.

Conditions

  • User Experience
  • Postoperative Complications
  • Acute Medical Conditions

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    collaborator OTHER

  • Christian S. Meyhoff

    lead OTHER

Principal Investigators

  • Christian S Meyhoff, MD, PhD · Copenhagen University Hospital - Bispebjerg and Frederiksberg, Copenhagen, Denmark

  • Eske K Aasvang, MD, DMSci · Rigshospitalet, Copenhagen University, Copenhagen, Denmark

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-26
Primary Completion
2026-08-01
Completion
2026-12-31

Countries

  • United States
  • Germany
  • Netherlands
  • Norway
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06289699 on ClinicalTrials.gov