At the top of this page, you can click on the "Participate" button. This will redirect you to information about the TRAPHEAC study and the "I want to participate" button. By clicking on this button, you will be asked to enter your e-mail address.
Once you have entered and validated your e-mail address in the field, you will receive an automatic message containing your personal identifiers (login and password), as well as the link to the study's Internet portal page. Your login details will enable you to connect to the portal at any time.
On the portal, you'll find all the information you need about the study and the protection and confidentiality of your data.
To finalize your registration, you should:
- To confirm your eligibility for TRAPHEAC
- To confirm your consent to participate in the study
- To enter your identifying information
Once you have filled in these details, you will be redirected to the questionnaires, which you can fill in from any connected device (computer, tablet, smartphone). The initial questionnaire takes 50 to 60 minutes to complete and you will have 1 month to complete it.
You will then be included in the TRAPHEAC. You will then receive much shorter update questionnaires every 6 to 12 months for several years.
Our aim is to improve our knowledge of your working conditions and how they have changed over time. We also want to know more about the impact they have on your health, so that we can put forward recommendations to help you work in good conditions and feel good at work.
That's where you come in. By participating, you become an actor in your own change.
A cohort is a group of participants involved in a research study over a specific period, often several years.
Members of TRAPHEAC regularly asked questions about their working conditions and career, their health and their life balance. Participants are tracked over time, enabling us to observe whether or not changes in each of these factors develop. This approach gives us the opportunity to gain an in-depth understanding of how participants' working conditions evolve over time and their link with health in the profession.
Access to research data (pseudonymized, de-identified and coded) will not be public. Only members of the project team responsible for data collection, analysis and scientific interpretation will have access, in accordance with the regulations and framework approved by the relevant ethics committee.
Access to identifying data will be restricted solely to the Unisanté IT service and the FSO. This access is subject to strict regulations and security procedures (e.g. only for IT maintenance operations).