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Trends of Patient-reported Outcome Measures (PROMs) in Multimorbid Medical Patients Hospitalized for an Acute Illness

NCT06597318 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2024-09-19

No results posted yet for this study

Summary

currently, PROMs and PREMs are not routinely collected and compared among medical inpatients of Swiss university hospitals, nor is a standard set of PROMs and PREMs available for use in Swiss hospitals. The project aims to examine trends in patient-reported outcomes (PROMs), including symptoms, quality of life, and distress, in multimorbid hospitalized patients from admission to 30 days post-discharge. It will also investigate whether PROMs at discharge are linked to the risk of readmission or emergency visits and explore how these outcomes differ in patients who receive low-value care. Additionally, the project will assess the relationship between patient-reported experiences (PREMs) and the provision of low-value care during the hospital stay.

Conditions

  • PROM
  • PREM
  • Quality of Care
  • Internal Medicine

Interventions

OTHER

Hospitalization

The investigators collect PROMs amongst up to 1000 patients in general internal medicine divisions of all five Swiss university hospitals

Sponsors & Collaborators

  • Insel Gruppe AG, University Hospital Bern

    collaborator OTHER

  • University Hospital, Geneva

    collaborator OTHER

  • University Hospital, Zürich

    collaborator OTHER

  • University Hospital, Basel, Switzerland

    collaborator OTHER

  • University of Lausanne Hospitals

    lead OTHER

Principal Investigators

  • Jerome Stirnemann, MD · University Hospital, Geneva

  • Carole Aubert, MD · Bern University Hospital

  • Florence Vallelian Cervetto, MD · Zürich University Hospital

  • Stefano Bassetti, MD · Basel University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-01
Primary Completion
2025-08-31
Completion
2025-10-01

Countries

  • Switzerland

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 NCT06597318 on ClinicalTrials.gov