Alerts
PDF
Other content recommended for you
- What does ‘respect for persons’ require? Attitudes and reported practices of genetics researchers in informing research participants about research
- Research for Health Justice: an ethical framework linking global health research to health equity
- Inclusion of adults with conditions that have the potential to affect capacity and or communication in research: triangulation from a mixed-methods study of current practice and values across multiple stakeholders
- Education versus screening: the use of capacity to consent tools in psychiatric genomics
- Healthcare professionals’ and researchers’ understanding of cancer genetics activities: a qualitative interview study
- Using digital tools in clinical, health and social care research: a mixed-methods study of UK stakeholders
- An investigation of patients’ motivations for their participation in genetics-related research
- Impacts of clinical academic activity: qualitative interviews with healthcare managers and research-active nurses, midwives, allied health professionals and pharmacists
- Exploring the experiences of substitute decision-makers with an exception to consent in a paediatric resuscitation randomised controlled trial: study protocol for a qualitative research study
- ‘Who is going to put their life on the line for a dollar? That’s crazy’: community perspectives of financial compensation in clinical research