NCT05884788

Brief Summary

This study wishes to focus on the life course of patients, beyond the moments of suffering experienced at the time of the request for euthanasia. It is based on the perspective that the patient's account of his or her life course can be a source of information for better understanding and accompanying patients requesting euthanasia.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
7

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jun 2023

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 9, 2023

Completed
23 days until next milestone

First Posted

Study publicly available on registry

June 1, 2023

Completed
Same day until next milestone

Study Start

First participant enrolled

June 1, 2023

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2024

Completed
Last Updated

April 16, 2025

Status Verified

April 1, 2025

Enrollment Period

1.2 years

First QC Date

May 9, 2023

Last Update Submit

April 11, 2025

Conditions

Keywords

EuthanasiaCancer

Outcome Measures

Primary Outcomes (1)

  • Description of the life stories of patients requesting euthanasia to explore which life experiences are brought forward when making this request, in a context of advanced oncological pathology.

    The main objective is to describe the life stories of patients requesting euthanasia in order to discover which life experiences are reasoning in the formulation of this request, in a context of advanced oncological pathology. The investigators carry out a descriptive analysis of the interviews. The interviews will be analyzed as they are conducted, in order to identify themes of interest. The themes will be compared between the different interviews in order to identify possible trends.

    One month

Secondary Outcomes (2)

  • Calculation of the Bartholomew score

    One month

  • Calculation of the distress thermometer's score

    One month

Interventions

After inclusion in the study, patients will be met for a free interview. The interview will be conducted using an open-ended interview method with the patients to allow free expression of their life history, using open and broad questions to avoid the influence of the interviewer as much as possible. Each interview will be conducted by the same person to allow for better interpersonal reproducibility. After the interview, the patients will be seen again to complete two questionnaires: * An attachment questionnaire: Relationship Scales Questionnaire * A questionnaire on symptoms: Distress thermometer

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

We conduct our study in a French cancer center and a French public hospital. Patients requesting euthanasia will be informed about the possibility of participating in our study. If the patients agree, and if they meet the study criteria, they will be included.

You may qualify if:

  • Major patients
  • With cancer in the palliative phase, i.e. with an incurable disease according to current knowledge.
  • Expressing a request for euthanasia in terms evoking a request for death with the intervention of an outside person.
  • Non-opposition to the study after full written information.

You may not qualify if:

  • Severe decompensated psychiatric pathology
  • Vulnerable persons defined here as pregnant women, parturients and persons under legal protection or unable to express their consent
  • Inability to conduct an interview

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Léon Bérard

Lyon, 69008, France

Location

MeSH Terms

Conditions

Suicide, AssistedNeoplasms

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 9, 2023

First Posted

June 1, 2023

Study Start

June 1, 2023

Primary Completion

July 31, 2024

Study Completion

July 31, 2024

Last Updated

April 16, 2025

Record last verified: 2025-04

Locations