Table 2.
Themes addressed during interviews and focus groups
| Interviews with patients |
Understanding of the biobank’s functioning and purpose Understanding of broad consent Information provided by the biobank recruiter Perception of biological material Data confidentiality Decision-making process Return of individual research results Personal expectations and suggestions |
| Focus groups |
Contextual factors relevant to broad consent practice Perception of recruiter’s role Patient’s decision-making process Perception of the biobank mission |