Actively Recruiting

Age: 18Years +
All Genders
NCT06597318

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

Led by University of Lausanne Hospitals · Updated on 2024-09-19

1000

Participants Needed

1

Research Sites

117 weeks

Total Duration

On this page

Sponsors

U

University of Lausanne Hospitals

Lead Sponsor

I

Insel Gruppe AG, University Hospital Bern

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Eligible for the LUCID registry: age 18 or older, hospitalized in one of the five participating Swiss university hospitals (Geneva, Lausanne, Bern, Zürich, Basel) after 01.01.2014, and admitted to general internal medicine wards
  • Have two or more chronic diseases lasting at least 6 months or based on clinical decision
  • Hospitalized for an acute illness
  • Signed the study-specific informed consent
Not Eligible

You will not qualify if you...

  • Unable to speak French, German, or English
  • Expected hospital stay less than 4 days
  • Previously included in the TRADUCE study
  • Cognitive impairment that affects ability to complete patient-reported outcome measures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Lausanne University Hospital

Lausanne, Canton of Vaud, Switzerland, 1005

Actively Recruiting

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Research Team

M

Marie Méan, MD

CONTACT

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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