NCT02845817

Brief Summary

This study take place in the palliative care units of Burgundy-Franche-Comté regions and at the Maison Médicale Jeanne Garnier. The main aim of this project is to analyze and understand the meaning of explicit requests to hasten death (euthanasia and assisted suicide). This involves conducting interviews with patients, carers to whom the request has been expressed and a relative chosen by the patient. This study aims to describe the request over time. This will be done through two series of interviews, one as soon as it is first expressed, then one week later.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
31

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2014

Shorter than P25 for not_applicable

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2014

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2015

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

July 18, 2016

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 27, 2016

Completed
Last Updated

July 27, 2016

Status Verified

July 1, 2016

Enrollment Period

9 months

First QC Date

July 18, 2016

Last Update Submit

July 26, 2016

Conditions

Outcome Measures

Primary Outcomes (1)

  • 70 semi-structured interviews

    Qualitative data analysis - Theoretical concept saturation and thematic analyses. \[analyze and understand the meaning of explicit requests to hasten death (euthanasia and assisted suicide)\]

    12 months

Study Arms (1)

Qualitative research

OTHER

Semi-structured interviews

Other: Qualitative research

Interventions

Semi-structured interviews

Qualitative research

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Adult not under guardianship or curatorship,
  • Hospitalized in palliative care units of Bourgogne-Franche-Comté region and in the Maison Médicale Jeanne Garnier in Paris,
  • At the end of life due to advanced stage disease or a major change in the state of health of an elderly person,
  • They have made an explicit request for euthanasia or assisted suicide,
  • They are in capacity to meet researchers for interview,
  • Having consented to interviews,
  • They are covered by the French social security system.

You may not qualify if:

  • Adult under guardianship or curatorship,
  • They are underage,
  • They are not hospitalized in Palliative Care Unit of Bourgogne-Franche-Comté region and in the Maison Médicale Jeanne Garnier,
  • The request was expressed by another person or not explicit,
  • They didn't consent to interviews,
  • The request appears in the context of a situation other than illness or a general change in state of health
  • They are not in capacity to meet researchers for interviews.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHRU Besançon - Palliative Care Unit

Besançon, Bourgogne-Franche-Comté, 25000, France

Location

MeSH Terms

Conditions

DeathSuicide, Assisted

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsSuicideSelf-Injurious BehaviorBehavioral SymptomsBehavior

Study Officials

  • Régis AUBRY, PR

    Centre Hospitalier Universitaire de Besançon

    PRINCIPAL INVESTIGATOR
  • Danièle LEBOUL, MCU

    Maison Médicale Jeanne Garnier

    PRINCIPAL INVESTIGATOR
  • Frédéric GUIRIMAND, DR

    Maison Médicale Jeanne Garnier

    PRINCIPAL INVESTIGATOR
  • Aline CHASSAGNE, IRC

    Centre Hospitalier Universitaire de Besançon

    PRINCIPAL INVESTIGATOR
  • Florence MATHIEU-NICOT, Phd

    Centre Hospitalier Universitaire de Besançon

    PRINCIPAL INVESTIGATOR
  • Anne BOUSQUET, Phd

    Maison Médicale Jeanne Garnier

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 18, 2016

First Posted

July 27, 2016

Study Start

September 1, 2014

Primary Completion

June 1, 2015

Study Completion

June 1, 2015

Last Updated

July 27, 2016

Record last verified: 2016-07

Locations