Requests for Euthanasia and Assisted Suicide (EPIDESA2)

Requests for Euthanasia and Assisted Suicide : Epidemiological Study Conducted as Part of the Establishment of a Structured Network

The study epiDESA2 identifies all explicit requests for euthanasia or assisted suicide expressed by the person him/herself, regardless of which professional is asked and regardless of where the request is made (primary care, health institutions, medico-social institutions including nursing home care or at home) in the Burgundy-Franche-Comté region during six months.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

65

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Besancon, France, 25000
        • CHRU Besançon

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The study epiDESA2 identifies all explicit requests for euthanasia or assisted suicide expressed by the person him/herself regardless of where the request is made (primary care, health institutions, medico-social institutions including EHPADs or at home) in the regions of Burgundy-Franche-Comté during six months.

Description

Inclusion Criteria:

Any adult :

  • Living at home, or in medico-social institutions or hospitalized in primary care or health institutions of Burgundy-Franche-Comté,
  • At the end of life due to advanced stage disease or a major change in the state of health of an elderly person,
  • Who expressed an explicit request for euthanasia or assisted suicide,
  • Who expressed their no objection to the collection of their datas,
  • Who are covered by the French social security system.

Exclusion Criteria:

  • They are underage
  • The request was expressed by another person
  • The request is not an explicit request
  • The request appears in the context of a situation other than illness or a general change in state of health
  • The patient is mentally confused

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Census of requests for euthanasia or assisted suicide in Burgundy-Franche-Comté
Time Frame: 6 months
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2017

Primary Completion (Actual)

December 31, 2017

Study Completion (Actual)

December 31, 2017

Study Registration Dates

First Submitted

July 19, 2016

First Submitted That Met QC Criteria

July 21, 2016

First Posted (Estimate)

July 26, 2016

Study Record Updates

Last Update Posted (Actual)

July 17, 2018

Last Update Submitted That Met QC Criteria

July 16, 2018

Last Verified

July 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • EPIDESA2

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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