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Approaches and experiences implementing remote, electronic consent at the Leeds Clinical Trials Research Unit.
William J Cragg1, Chris Taylor2, Lauren Moreau2
1Clinical Trials Research Unit, Leeds Institute of Clinical Trials Research, University of Leeds, Leeds, UK. w.cragg@leeds.ac.uk.
Electronic informed consent (eConsent) implementation at Leeds CTRU improved participant access and trial resilience. Site-level factors, not patient preference, influenced eConsent uptake, highlighting areas for process enhancement.
Area of Science:
- Clinical research methodology
- Health informatics
- Regulatory science
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