Appropriate Medication Use in Dutch Terminal Care

NCT05351281 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2025-03-21

No results posted yet for this study

Summary

The AMUSE trial is a multicentre stepped-wedge cluster randomized controlled trial where medication optimization of patients with a life expectancy of less than three months is investigated by using CDSS-OPTIMED (a personalized medication advice to attending physicians of patients in the last phase of life) The investigators will include 250 patients, in 7 different study sites across the Netherlands. The primary outcome is an assessment of the quality of life of patients, two weeks after baseline assessment.

Conditions

  • Palliative Care
  • Terminal Care
  • Medication Therapy Management
  • Clinical Decision Support System (CDSS)
  • Quality of Life

Interventions

DEVICE

CDSS-OPTIMED

The CDSS-OPTIMED is a software program that provides the physician with a personalized alert on whether to consider stopping or starting medication for a specific patient with a life expectancy of less than 3 months.

Sponsors & Collaborators

  • Rijnstate Hospital

    collaborator OTHER
  • Ikazia Hospital, Rotterdam

    collaborator OTHER
  • Noordwest Ziekenhuisgroep

    collaborator OTHER
  • Laurens Cadenza Zuid

    collaborator UNKNOWN
  • Nijmegen University Academic Network Family Medicine

    collaborator NETWORK
  • Gezondheidscentrum Krimpen

    collaborator UNKNOWN
  • Prof.dr Carin (C.C.D.) van der Rijt

    lead OTHER

Principal Investigators

  • Carin van der Rijt, Prof, MD · Erasmus Medical Center

  • Eric Geijteman, MD, PhD · Erasmus Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-29
Primary Completion
2024-10-16
Completion
2025-02-20

Countries

  • Netherlands

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 NCT05351281 on ClinicalTrials.gov