Cargando…
Research recruitment and consent methods in a pandemic: a qualitative study of COVID-19 patients’ perspectives
BACKGROUND: Virtual data collection methods and consent procedures adopted in response to the COVID-19 pandemic enabled continued research activities, but also introduced concerns about equity, inclusivity, representation, and privacy. Recent studies have explored these issues from institutional and...
Autores principales: | Small, Serena S, Lau, Erica, McFarlane, Kassandra, Archambault, Patrick M, Longstaff, Holly, Hohl, Corinne M |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173898/ https://www.ncbi.nlm.nih.gov/pubmed/37170077 http://dx.doi.org/10.1186/s12874-023-01933-5 |
Ejemplares similares
-
Patient Perspectives on Health Data Privacy and Implications for Adverse Drug Event Documentation and Communication: Qualitative Study
por: Small, Serena S, et al.
Publicado: (2021) -
Sharing Adverse Drug Event Reports Between Hospitals and Community Pharmacists to Inform Re-dispensing: An Analysis of Reports and Process Outcomes
por: Cragg, Amber, et al.
Publicado: (2023) -
Consent in escrow
por: Van der Loos, Kiah I., et al.
Publicado: (2014) -
Beliefs and perceptions of patient safety event reporting in a Canadian Emergency Department: a qualitative study
por: Skutezky, Trevor, et al.
Publicado: (2022) -
Recruiting for Epigenetic Research: Facilitating the Informed Consent Process
por: Jallo, Nancy, et al.
Publicado: (2013)