ClinicalTrials.gg
RecruitingNCT07895940PALLI-SMUR1Updated Oct 26, 2026

Prehospital Care of End-of-Life Patients by the Strasbourg Mobile Emergency and Resuscitation Service: A Qualitative Study of Healthcare Professionals' Experiences and Use of a Comfort Care Booklet

An observational study in End-of-life Care, Palliative Care and Prehospital Emergency Care, sponsored by University Hospital, Strasbourg, France. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by University Hospital, Strasbourg, France · Observational

From the registry’s dates

  • Started Mar 2026; still recruiting 7 months later.
Updated Oct 26, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
20
Ages
18 Years and older
Sex
All
01

Study summary

Prehospital end-of-life care presents complex clinical, ethical, relational, and organizational challenges for healthcare professionals working in the Strasbourg Mobile Emergency and Resuscitation Service (SMUR). A comfort care booklet was introduced in the service in March 2025 to harmonize practices and improve the quality of palliative care delivered in the prehospital setting. However, professionals' experiences, perceptions of the booklet, its perceived impact on practice, and their needs have not yet been explored.

This qualitative descriptive study will explore the experiences, perceptions, and needs of SMUR healthcare professionals regarding prehospital end-of-life care and the implementation of the comfort care booklet. Individual semi-structured face-to-face interviews will be conducted, audio-recorded, transcribed anonymously, and analyzed using an inductive thematic approach. Approximately 12 to 20 participants will be recruited through purposive sampling, with recruitment continuing until data saturation is reached.

02

Conditions studied

  • End-of-life Care
  • Palliative Care
  • Prehospital Emergency Care
  • Healthcare Professionals' Experiences and Perceptions
  • Comfort Care Booklet Implementation

Keywords

  • Prehospital end-of-life care
  • Comfort care booklet
  • Qualitative study
03

In context

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 994 studies on the registry; 353 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

Healthcare professionals currently working in the Strasbourg Mobile Emergency and Resuscitation Service at Strasbourg University Hospitals, including physicians, nurse anesthetists, registered nurses, and ambulance personnel. Participants will be purposively sampled to represent different professional roles, levels of experience, and work patterns, including exclusively SMUR activity or mixed activity. Recruitment will continue until data saturation, with an estimated sample size of 12 to 20 participants.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Healthcare professionals currently working in the Strasbourg SMUR at Strasbourg University Hospitals, including physicians, nurse anesthetists, registered nurses, and ambulance personnel.
  • At least three months of SMUR experience.
  • Voluntary agreement to participate in the study.

Exclusion criteria

Exclusion Criteria:

  • Professionals in a probationary period.
  • Administrative or logistics personnel.
  • Individuals who decline participation after receiving study information.
  • Individuals who decline audio recording of the interview.
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
20 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Data saturation regarding perceptions of prehospital end-of-life care and use of the comfort care booklet

    Achievement of data saturation for the main themes emerging from qualitative interviews with SMUR healthcare professionals concerning their experiences, perceptions, needs, and use of the comfort care booklet in prehospital end-of-life care.

    Time frame: From study initiation until data saturation, estimated within 6 months of data collection.

Secondary outcomes

  1. Perceived usefulness and practicality of the comfort care booklet

    Diversity and recurrence of professional opinions regarding the booklet's usefulness, practicality, and integration into clinical practice.

    Time frame: During the 6-month data collection period.

  2. Reported difficulties and improvement needs in prehospital end-of-life care

    Identification of difficulties encountered by different professional groups, concrete proposals for improvement, and needs for additional tools or training.

    Time frame: During the 6-month data collection period.

07

Study locations

1 of 1 sites recruiting
  • SMUR de Strasbourg - CHU de Strasbourg, France
    Strasbourg, 67091, France
    • Valérie Wilmé, MD · Contact · valerie.wilme@chru-strasbourg.fr · 33 6 89 13 46 64
    • Valérie Wilmé, MD · Principal investigator
    • Quentin MITOIRE, Nurse · Sub investigator
    • Anne WEISS, MD · Sub investigator
    Recruiting
08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Mar 2026 (actual). Primary completion is estimated for Jan 2027, 10 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 19, 2026
First posted
Oct 26, 2026
StartActual
Mar 6, 2026
Primary completionEst.
Jan 6, 2027
CompletionEst.
Mar 6, 2027
Last update
Oct 26, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 26, 2026
Show all 1 update
  1. Oct 26, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07895940
Responsible party
Sponsor
First posted
Oct 26, 2026
Start date
Mar 6, 2026
Primary completion
Jan 6, 2027 (estimated)
Completion
Mar 6, 2027 (estimated)
Last update
Oct 26, 2026

Study contacts

Valérie Wilmé, MD
Contact
valerie.wilme@chru-strasbourg.fr
33 6 89 13 46 64

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

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