I contribute
you want to take part in one of our studies, please contact us
My path in a study
All studies carried out within the team are evaluated and validated by an ethics committee. We are particularly vigilant in ensuring that the rights of the persons involved in our research are strictly respected. A typical research process is as follows:
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The study is presented to me in a clear and comprehensible manner;
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My eligibility for the study is checked (inclusion and non-inclusion criteria);
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I am given a briefing note outlining the details of the study;
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After consideration, I give my written consent to participate (I keep a copy of this consent);
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My participation (or not) in the study in no way affects the quality of care I will receive as part of a medical follow-up;
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INCLUSION: this is when I enter the study, according to the procedures defined in the protocol;
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One or more visits are scheduled, during which I will be able to carry out tasks, undergo examinations or receive treatment, in accordance with the protocol I have approved;
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At any time during the study or follow-up, I can ask to prematurely withdraw from the study ;
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I may at any time request access to and rectification of my personal data;
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At the end of the study and at my request, I can be informed of the results;
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My anonymized data will be securely archived;
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I may at any time object to the re-use of this data in further research, or to being recontacted to take part in further research.