Early Maladaptive Schemas in French Health Care Professionals With Burn Out (NCT06104202) | Clinical Trial Compass
RecruitingNot Applicable
Early Maladaptive Schemas in French Health Care Professionals With Burn Out
France273 participantsStarted 2024-04-09
Plain-language summary
The purpose of this study is to compare the profiles and domains of maladaptive early schemas in care professionals with burnout symptoms with care professionals without burnout symptoms and with care non-professionals with burnout symptoms.
Who can participate
Age range
18 Years
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:
* Age ≥ 18 years ;
* State of burnout (at least one of the 3 dimensions of the Maslach Burnout Inventory) for care professionals and non-professionals in a state of burnout and absence of a state of burnout for the group of care professionals without a state of burnout;
* Membership of a social security scheme;
* Patient having been informed and having given his/her oral non-opposition.
Exclusion Criteria:
* Characterised psychiatric pathology pre-existing the burn out state for the burn out groups and characterised psychiatric pathology for the no burn out group;
* Participation in another clinical trial, or in a period of exclusion from another clinical trial;
* Participant under guardianship, curatorship or deprived of liberty.
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.
1This trial is looking at something called 'Early Maladaptive Schemas' in healthcare workers with burnout — can you explain what that means and whether understanding my own schemas could actually help my burnout recovery?
2The main measurement in this study is a questionnaire called the Young Schema Questionnaire Short Form — can you tell me what completing this questionnaire would involve for me, and how the results might or might not be used to guide my treatment?
3This trial is listed as 'Phase NA,' which suggests it's more of an observational or psychological study rather than a drug trial — does that change the risks involved, and what would actually be asked of me if I participated?
4Since this study is specifically for French healthcare professionals with burnout, can you help me understand whether my specific role and situation would even make me a suitable candidate to discuss with the research team?
5Are there other burnout treatments or support programs I should consider alongside or instead of participating in this study, given that this trial appears to be focused on data collection rather than delivering a specific therapy?
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
Young Schema Questionnaire Short form
Timeframe: 21 days
Trial details
NCT IDNCT06104202
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche