Feedback and Mental Well-being in Anesthesiology (NCT06667011) | Clinical Trial Compass
CompletedNot Applicable
Feedback and Mental Well-being in Anesthesiology
Belgium54 participantsStarted 2024-11-04
Plain-language summary
The aims of the study are:
* to evaluate the mental health of anesthesia trainees and teachers in the Cliniques universitaires Saint-Luc academic hospital;
* to evaluate the effect of a daily debriefing session between trainees and teachers on the mental health of the participants at the end of a trimester;
* to identify any personal and/or institutional factors that might hinder the implementation and successful running of these debriefing sessions within our teaching hospital.
The investigators will compare the data collected by questionnaires in the "intervention" group (daily debriefing) with a control group in which no debriefing will be carried out between trainees and teachers.
Who can participate
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Board-certified anesthesiologists (teachers) in the visceral, pediatric, orthopedic, or neuro-head-and-neck anesthesia areas at Cliniques Universitaires Saint-Luc.
* Anesthesia trainees assigned to the visceral, pediatric, orthopedic, and neuro-head-and-neck anesthesia departments from January 7 to April 7, 2025 at Cliniques Universitaires Saint-Luc.
Exclusion Criteria:
\- None.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Maslach Burn-out Inventory (MBI) score
Timeframe: up to 3 months
Trial details
NCT IDNCT06667011
SponsorCliniques universitaires Saint-Luc- Université Catholique de Louvain