HIGHLIGHTS
- who: Aude Le Bris from the The study was approved by the Rennes University Hospital Ethics Committee (reference number, ) and all participants gave their informed consent in writing before participating. A physician was responsible for explaining the research project to potential participants. The same physician also had to submit an email newsletter on the purpose and conduct of the research. Any individuals who expressed an interest in participating in the focus groups and who met the inclusion criteria were included. Participation was on a voluntary basis and participants were informed that they could withdraw their consent to . . .
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