Living Well, Dying Well. a Research Programme to Support Living Until the End

NCT04271085 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1500

Last updated 2025-03-11

No results posted yet for this study

Summary

The iLIVE project involves a cohort study in which patients with an estimated life expectancy of six months or less are followed until they die. In total, the investigators will include 2200 patients in 11 countries, i.e. 200 per country. The primary outcome for the cohort study is a descriptive assessment of the concerns, expectations and preferences around dying and end-of-life care of patients and their relatives, in different settings and cultures..

Conditions

  • Terminal Care

Interventions

OTHER

Observational study

No intervention involved

Sponsors & Collaborators

  • University of Liverpool

    collaborator OTHER
  • Klinikum der Universität Köln

    collaborator OTHER
  • Lund University

    collaborator OTHER
  • The University Clinic of Pulmonary and Allergic Diseases Golnik

    collaborator OTHER
  • University of Bern

    collaborator OTHER
  • Cudeca Hospice Foundation

    collaborator OTHER
  • Helse-Bergen HF

    collaborator OTHER
  • Landspitali University Hospital

    collaborator OTHER
  • Pallium Latinoamérica N.G.O

    collaborator OTHER
  • University of Humanistic Studies

    collaborator UNKNOWN
  • Medical University of Vienna

    collaborator OTHER
  • Arohanui Hospice Service Trust

    collaborator UNKNOWN
  • Erasmus Medical Center

    lead OTHER

Principal Investigators

  • Agnes van der Heide, PhD · Erasmus Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-09-01
Primary Completion
2023-07-31
Completion
2023-07-31

Countries

  • Argentina
  • Germany
  • Iceland
  • Netherlands
  • New Zealand
  • Norway
  • Slovenia
  • Spain
  • Sweden
  • Switzerland
  • United Kingdom

Study Locations

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Entities

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 NCT04271085 on ClinicalTrials.gov