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From patients to partners: participant-centric initiatives in biomedical research
Authors:Kaye Jane  Curren Liam  Anderson Nick  Edwards Kelly  Fullerton Stephanie M  Kanellopoulou Nadja  Lund David  MacArthur Daniel G  Mascalzoni Deborah  Shepherd James  Taylor Patrick L  Terry Sharon F  Winter Stefan F
Institution:HeLEX, Department of Public Health, University of Oxford, Old Road Campus, Headington, Oxford OX3 7LF, UK. jane.kaye@law.ox.ac.uk
Abstract:Advances in computing technology and bioinformatics mean that medical research is increasingly characterized by large international consortia of researchers that are reliant on large data sets and biobanks. These trends raise a number of challenges for obtaining consent, protecting participant privacy concerns and maintaining public trust. Participant-centred initiatives (PCIs) use social media technologies to address these immediate concerns, but they also provide the basis for long-term interactive partnerships. Here, we give an overview of this rapidly moving field by providing an analysis of the different PCI approaches, as well as the benefits and challenges of implementing PCIs.
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