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From Patients to Partners: Participant-centric Initiatives in Biomedical Research

Overview
Journal Nat Rev Genet
Specialty Genetics
Date 2012 Apr 5
PMID 22473380
Citations 122
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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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References
1.
Porter S, Forbes P, Manzi S, Kalish L . Patients providing the answers: narrowing the gap in data quality for emergency care. Qual Saf Health Care. 2010; 19(5):e34. DOI: 10.1136/qshc.2009.032540. View

2.
Feied C, Handler J, Smith M, Gillam M, Kanhouwa M, Rothenhaus T . Clinical information systems: instant ubiquitous clinical data for error reduction and improved clinical outcomes. Acad Emerg Med. 2004; 11(11):1162-9. DOI: 10.1197/j.aem.2004.08.010. View

3.
Trinidad S, Fullerton S, Bares J, Jarvik G, Larson E, Burke W . Genomic research and wide data sharing: views of prospective participants. Genet Med. 2010; 12(8):486-95. PMC: 3045967. DOI: 10.1097/GIM.0b013e3181e38f9e. View

4.
Teich J . The benefits of sharing clinical information. Ann Emerg Med. 1998; 31(2):274-6. DOI: 10.1016/s0196-0644(98)70318-x. View

5.
Terry S, Terry P . Power to the people: participant ownership of clinical trial data. Sci Transl Med. 2011; 3(69):69cm3. DOI: 10.1126/scitranslmed.3001857. View