CClinicalTrials.gg
CompletedNCT05884788RECIFEUpdated Apr 16, 2025

Study of the Life Stories of Patients Making a Request for Euthanasia, in the Context of Advanced Cancer.

An observational study in Advanced Cancer, sponsored by Centre Leon Berard. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-04-16.

Sponsored by Centre Leon Berard · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
7
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Advanced Cancer

Browse trials for

Keywords

  • Euthanasia
  • Cancer
03

In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

This study's enrollment of 7 is below the median of 204 across 1,683 observational studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

Centre Leon Berard is the lead sponsor of 206 studies on the registry; 61 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-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.

Inclusion criteria

  • 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.

Exclusion criteria

Exclusion Criteria:

  • 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
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
7 participants (actual)
Patient registry
No

Interventions

  • Otherfree interview, and questionnaires in a second time

    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

06

What researchers measure

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.

    Time frame: One month

Secondary outcomes

  1. Calculation of the Bartholomew score

    Use of specific questionnaire (Relationship Scales Questionnaire of Batholomew) to describe the profiles of the patients in the study

    Time frame: One month

  2. Calculation of the distress thermometer's score

    Use of specific questionnaire (NCCN distress thermometer) to describe the profiles of the patients in the study

    Time frame: One month

07

Study locations

1 site
  • Centre Léon Bérard
    Lyon, 69008, France
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 16, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05884788
Lead sponsor
Centre Leon Berard
Responsible party
Sponsor
First posted
Jun 1, 2023
Start date
Jun 1, 2023
Primary completion
Jul 31, 2024
Completion
Jul 31, 2024
Last update
Apr 16, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion