Cargando…
e-Consent in UK academic-led clinical trials: current practice, challenges and the need for more evidence
BACKGROUND: During the COVID-19 pandemic, in-person healthcare visits were reduced. Consequently, trial teams needed to consider implementing remote methods for conducting clinical trials, including e-Consent. Although some clinical trials may have implemented e-Consent prior to the pandemic, anecdo...
Autores principales: | Mitchell, E. J., Appelbe, D., Bravery, A., Culliford, L., Evans, H., Farrin, A. J., Gillies, K., Hood, K., Love, S. B., Sydes, M. R., Williamson, P. R., Wakefield, N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565982/ https://www.ncbi.nlm.nih.gov/pubmed/37817277 http://dx.doi.org/10.1186/s13063-023-07656-8 |
Ejemplares similares
-
Monitoring in practice – How are UK academic clinical trials monitored? A survey
por: Love, Sharon B., et al.
Publicado: (2020) -
Development of a measure to assess the quality of proxy decisions about research participation on behalf of adults lacking capacity to consent: the Combined Scale for Proxy Informed Consent Decisions (CONCORD scale)
por: Shepherd, Victoria, et al.
Publicado: (2022) -
The Evolution of Consent Law in the UK
por: Prasher, Sparsh, et al.
Publicado: (2015) -
More Needs to Be Done During the Informed Consent Process
por: Alfuzaie, Rashed
Publicado: (2022) -
An international core outcome set for evaluating interventions to improve informed consent to clinical trials: The ELICIT Study
por: Gillies, Katie, et al.
Publicado: (2021)