Death RecordsCANDELSNCT06910176
Confirming And Notifying Death
An observational study of Death Records, run by University Hospital, Strasbourg, France at 1 site in France.
Trial summary
Most physicians are confronted with the death of patients during their practice, often as early as residency. It is their legal responsibility to certify a patient's death, as well as often to notify their loved ones. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Death Records
- How many people
- 20 participants
- Where
- 1 siteFrance
- Study dates
- 10 Oct 2024to 10 Dec 2025
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Student having taken the national ECOS (thus becoming an intern at the start of the following academic year in November 2024),
Who may be able to join
- DFASM3 student,
- At the Faculty of Medicine of Strasbourg, France, for the 2023-2024 academic year,
- Having taken the national ECOS (thus becoming an intern at the start of the following academic year in November 2024),
- Aged 18 years or older,
- Not opposed to participating in the study.
- Not having completed an internship in specialized palliative care facilities
Who cannot join
- Refused to participate in the study.
- Not having taken the national ECOS.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
France1 site, 1 recruiting
- Recruiting
Service de soins Palliatifs - CHU de Strasbourg - France
Strasbourg, 67091
Catherine CHEVALIER-LAMOUILLE, MD, 33 3 88 11 65 86, catherine.lamouille@chru-strasbourg.fr
Catherine CHEVALIER-LAMOUILLE, MD
About this study
Official title: Confirming And Notifying Death : Blended Learning and Its Evaluation by Medical Students, an Acceptability Study"
Most physicians are confronted with the death of patients during their practice, often as early as residency. It is their legal responsibility to certify a patient's death, as well as often to notify their loved ones.
Yet, these duties currently receive little or no specific training during the various cycles of medical education.
This task is not easy, however, and young professionals experience it with difficulty. Literature data show that residents are confronted with death late in their medical education and that they are insufficiently prepared when they have to perform their first death certificate. Indeed, residents report significantly correlated practical and emotional difficulties. These difficulties are notably linked to a feeling of lack of preparation through theoretical courses, a lack of familiarity with administrative procedures, and insufficient mastery of communicating with families. The highlighting of these difficulties and the desire for appropriate and respectful care for the deceased and their families, for whom the moment of announcement influences the experience of grief, call for an improvement in teaching on these topics. It is in this sense that the project was born to explore whether the creation of training, before their independent exposure to death and its announcement, i.e. at the end of the second cycle, was relevant. A prerequisite for this type of training project is indeed to question the acceptability of such an approach by students.
- Conditions
- Death Records
- Keywords
- Notifying Death, Death Records
What is being measured
The primary outcome is the main question the study is designed to answer.
To assess the acceptability of training in death certification and death notification to relatives by DFASM3 students in Strasbourg.
Measured: At 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Apr 2025
- Study start10 Oct 2024
- Primary completion10 Dec 2025 (estimated)
- Study completion10 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Death RecordsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 20 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University Hospital, Strasbourg, France
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06910176
- Sponsor's protocol ID
- 9304
- Acronym
- CANDELS
- Status last verified
- Mar 2025
- First submitted
- 27 Mar 2025
- Last updated
- 26 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Confirming And Notifying Death : Blended Learning and Its Evaluation by Medical Students, an Acceptability Study"
- ClinicalTrials.gov ID
- NCT06910176
- Acronym / sponsor ID
- CANDELS / 9304
- Conditions
- Death Records
- Keywords
- Notifying Death, Death Records
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 20 participants (estimated)
- Lead sponsor
- University Hospital, Strasbourg, FranceUniversity, hospital or other
- Study start
- 10 Oct 2024 (actual)
- Primary completion
- 10 Dec 2025 (estimated)
- Study completion
- 10 Dec 2025 (estimated)
- First posted
- 4 Apr 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Most physicians are confronted with the death of patients during their practice, often as early as residency. It is their legal responsibility to certify a patient's death, as well as often to notify their loved ones.
Yet, these duties currently receive little or no specific training during the various cycles of medical education.
This task is not easy, however, and young professionals experience it with difficulty. Literature data show that residents are confronted with death late in their medical education and that they are insufficiently prepared when they have to perform their first death certificate. Indeed, residents report significantly correlated practical and emotional difficulties. These difficulties are notably linked to a feeling of lack of preparation through theoretical courses, a lack of familiarity with administrative procedures, and insufficient mastery of communicating with families. The highlighting of these difficulties and the desire for appropriate and respectful care for the deceased and their families, for whom the moment of announcement influences the experience of grief, call for an improvement in teaching on these topics. It is in this sense that the project was born to explore whether the creation of training, before their independent exposure to death and its announcement, i.e. at the end of the second cycle, was relevant. A prerequisite for this type of training project is indeed to question the acceptability of such an approach by students.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Student having taken the national ECOS (thus becoming an intern at the start of the following academic year in November 2024),
Key inclusion criteria (6 listed)
- DFASM3 student,
- At the Faculty of Medicine of Strasbourg, France, for the 2023-2024 academic year,
- Having taken the national ECOS (thus becoming an intern at the start of the following academic year in November 2024),
- Aged 18 years or older,
- Not opposed to participating in the study.
Key exclusion criteria (2 listed)
- Refused to participate in the study.
- Not having taken the national ECOS.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
To assess the acceptability of training in death certification and death notification to relatives by DFASM3 students in Strasbourg.
Time frame: At 6 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Sep 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Death Records, run by University Hospital, Strasbourg, France at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 26 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Catherine CHEVALIER-LAMOUILLE, MD (33 3 88 11 65 86, catherine.lamouille@chru-strasbourg.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To assess the acceptability of training in death certification and death notification to relatives by DFASM3 students in Strasbourg. (time frame: At 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Sep 2025.