Preventing Burnout Among Caregivers Through Physical Activity (NCT06815484) | Clinical Trial Compass
CompletedNot Applicable
Preventing Burnout Among Caregivers Through Physical Activity
France75 participantsStarted 2025-03-12
Plain-language summary
The purpose of this study is to evaluate the impact of an adaptive physical activity programme to prevent the risk of burnout at the end of the programme (10 weeks after the start of the intervention).
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 ;
* Non-physician health professionals at the Clinique de la Sauvegarde ;
* Low or moderate level of physical activity, as assessed by the questionnaire International Physical Activity Questionnaire. In fact, work-related physical activity is not associated with a reduction in burnout ;
* Absence of serious chronic pathology incompatible with the physical activity of the protocol ;
* Willing and available to commit to the project for the duration of the study ;
* Using a personal smartphone or tablet and with an Internet connection ;
* Able to read, write and understand French ;
* Membership of a social security scheme.
Exclusion Criteria:
* High level of physical activity (not including work-related physical activity) ;
* Contraindication to physical activity (uncontrolled hypertension, uncontrolled heart disease...) ;
* Concurrent participation in another physical activity study ;
* Pregnant or likely to be pregnant ;
* Unable to be monitored for medical, social, family, geographical or psychological reasons for the duration of the study ;
* Persons deprived of their liberty by judicial or adm inistrative decision, or adults protected by law.
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
Shirom - Melamed Burnout Measure
Timeframe: 10 weeks
Trial details
NCT IDNCT06815484
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche