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  1. Scoping review and thematic analysis of informed consent in humanitarian emergencies.Benjamin Thomson, S. Mehta & C. Robinson - 2024 - BMC Medical Ethics 25 (1):1-14.
    Background To identify and to summarize challenges related to the informed consent process for research completed during humanitarian emergencies. Methods Using relevant search terms, a search of 5 databases was completed, without language, date, or study type restriction. Studies were screened for inclusion, with eligible studies being those that were relevant to the informed consent process for research studies completed in humanitarian emergencies. A Grounded Theory Analysis was completed to identify themes and subthemes. Results Review identified 30 relevant studies. We (...)
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  • Biobanking and consenting to research: a qualitative thematic analysis of young people’s perspectives in the North East of England.Momodou Ndure, Isatou Sarr, Anna Roca, Kalifa Bojang, Effua Usuf, Fiona Cresswell, Elizabeth Fitchett, David Bath, Manuel Dewez, Shunmay Yeung, Sebastian Schroepf, Carola Schoen, Karl Reiter, Esther Maier, Eberhard Lurz, Matthias Kappler, Sabrina Juranek, Tobias Feuchtinger, Matthias Griese, Florian Hoffmann, Niklaus Haas, Katharina Danhauser, Irene Alba-Alejandre, Ioanna Mavridi, Patricia Schmied, Laura Kolberg, Ulrich von Both, Maike K. Tauchert, Elmar Wallner, Volker Strenger, Andrea Skrabl-Baumgartner, Siegfried Rödl, Klaus Pfurtscheller, Andreas Pfleger, Heidemarie Pilch, Tobias Niedrist, Sabine Löffler, Markus Keldorfer, Andreas Kapper, Christa Hude, Almuthe Hauer, Harald Haidl, Siegfried Gallistl, Ernst Eber, Astrid Ceolotto, Martin Benesch, Sebastian Bauchinger, Manfred G. Sagmeister, Martina Strempfl, Bianca Stoiser, Glorija Rajic, Alexandra Rusu, Lena Pölz, Manuel Leitner, Susanne Hösele, Christoph Zurl, Nina A. Schweintzger, Daniel S. Kohlfürst, Benno Kohlmaier & Ale Binder - 2023 - BMC Medical Ethics 24 (1):1-11.
    BackgroundBiobanking biospecimens and consent are common practice in paediatric research. We need to explore children and young people’s (CYP) knowledge and perspectives around the use of and consent to biobanking. This will ensure meaningful informed consent can be obtained and improve current consent procedures.MethodsWe designed a survey, in co-production with CYP, collecting demographic data, views on biobanking, and consent using three scenarios: 1) prospective consent, 2) deferred consent, and 3) reconsent and assent at age of capacity. The survey was disseminated (...)
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  • A comprehensive systematic review of stakeholder attitudes to alternatives to prospective informed consent in paediatric acute care research.Jeremy Furyk, Kris McBain-Rigg, Bronia Renison, Kerrianne Watt, Richard Franklin, Theophilus I. Emeto, Robin A. Ray, Franz E. Babl & Stuart Dalziel - 2018 - BMC Medical Ethics 19 (1):89.
    A challenge of performing research in the paediatric emergency and acute care setting is obtaining valid prospective informed consent from parents. The ethical issues are complex, and it is important to consider the perspective of participants, health care workers and researchers on research without prospective informed consent while planning this type of research. We performed a systematic review according to PRISMA guidelines, of empirical evidence relating to the process, experiences and acceptability of alternatives to prospective informed consent, in the paediatric (...)
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  • Written versus verbal consent: a qualitative study of stakeholder views of consent procedures used at the time of recruitment into a peripartum trial conducted in an emergency setting.J. Lawton, N. Hallowell, C. Snowdon, J. E. Norman, K. Carruthers & F. C. Denison - 2017 - BMC Medical Ethics 18 (1):36.
    Obtaining prospective written consent from women to participate in trials when they are experiencing an obstetric emergency is challenging. Alternative consent pathways, such as gaining verbal consent at enrolment followed, later, by obtaining written consent, have been advocated by some clinicians and bioethicists but have received little empirical attention. We explored women’s and staff views about the consent procedures used during the internal pilot of a trial, where the protocol permitted staff to gain verbal consent at recruitment. Interviews with staff (...)
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