Consent in Research in an Emergency Setting, keynote talk by Victoria Shepherd
References
Articles
Davies, H., Shakur, H., Padkin, A., et al. (2014). Guide to the design and review of emergency research when it is proposed that consent and consultation be waived. Emergency Medicine Journal 31:794-795. http://dx.doi.org/10.1136/emermed-2014-203675
Shahzad, A., Kemp, I., Mars, C. et al. (2014). Unfractionated heparin versus bivalirudin in primary percutaneous coronary intervention (HEAT-PPCI): an open-label, single centre, randomised controlled trial. The Lancet 384(9957), 1849-1858. https://doi.org/10.1016/S0140-6736(14)60924-7
Shepherd, V. (2020) An under-represented and underserved population in trials: methodological, structural, and systemic barriers to the inclusion of adults lacking capacity to consent. Trials 21. https://doi.org/10.1186/s13063-020-04406-y
Shepherd, V., Hood, K., Wood, F. (2022). Unpacking the ‘Black Box of Horrendousness’: A Qualitative Exploration of the Barriers and Facilitators to Conducting Trials Involving Adults Lacking Capacity to Consent. [Preprint] https://doi.org/10.21203/rs.3.rs-1180306/v1
Other Resources
Adults with Incapacity (Scotland) Act 2000
Capacity and Consent Research website
Deferred consent in Emergency Research-A patient video
Good Clinical Practice Network 4.1 INVESTIGATOR
Mental Capacity Act 2005 (England + Wales)
MRC-NIHR Trials Methodology Research Partnership (TMRP) website
NHS Health Research Authority. Applying a proportionate approach to the process of seeking consent
NHS Health Research Authority. Confidentiality Advisory Group
NHS Health Research Authority. Research in Emergency Settings
NIHR. Improving inclusion of under-served groups in clinical research: Guidance from INCLUDE project
The Medicines for Human Use (Clinical Trials) Regulations 2004
UKRI & NHS Health Research Authority. Is my study research?
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