- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02845817
Requests for Euthanasia and Assisted Suicide (DESA)
Requests for Euthanasia and Assisted Suicide: a Prospective, Multicenter and Qualitative Study of Their Frequency and Characteristics, of Patients' Motivations and Their Evolution
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.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Bourgogne-Franche-Comté
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Besançon, Bourgogne-Franche-Comté, France, 25000
- CHRU Besançon - Palliative Care Unit
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
Study Plan
How is the study designed?
Design Details
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Qualitative research
Semi-structured interviews
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Semi-structured interviews
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
70 semi-structured interviews
Time Frame: 12 months
|
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
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Régis AUBRY, Pr, Centre Hospitalier Universitaire de Besancon
- 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 Besancon
- Principal Investigator: Florence MATHIEU-NICOT, Phd, Centre Hospitalier Universitaire de Besancon
- Principal Investigator: Anne BOUSQUET, Phd, Maison Médicale Jeanne Garnier
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DESA
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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