- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05884788
Study of the Life Stories of Patients Making a Request for Euthanasia, in the Context of Advanced Cancer. (RECIFE)
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Lyon, France, 69008
- Centre Léon Bérard
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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:
- 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
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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.
Time Frame: One month
|
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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Calculation of the Bartholomew score
Time Frame: One month
|
Use of specific questionnaire (Relationship Scales Questionnaire of Batholomew) to describe the profiles of the patients in the study
|
One month
|
|
Calculation of the distress thermometer's score
Time Frame: One month
|
Use of specific questionnaire (NCCN distress thermometer) to describe the profiles of the patients in the study
|
One month
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ET22000324
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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