[HTML][HTML] Using clinical natural language processing for health outcomes research: overview and actionable suggestions for future advances

S Velupillai, H Suominen, M Liakata, A Roberts… - Journal of biomedical …, 2018 - Elsevier
The importance of incorporating Natural Language Processing (NLP) methods in clinical
informatics research has been increasingly recognized over the past years, and has led to …

Electronic consenting for conducting research remotely: A review of current practice and key recommendations for using e-consenting

E Skelton, N Drey, M Rutherford, S Ayers… - International journal of …, 2020 - Elsevier
Background Electronic approaches are becoming more widely used to obtain informed
consent for research participation. Electronic consent (e-consent) provides an accessible …

Privacy, confidentiality, security and patient safety concerns about electronic health records

W Bani Issa, I Al Akour, A Ibrahim… - International nursing …, 2020 - Wiley Online Library
Aims This study explored concerns among nurses working in the United Arab Emirates
associated with the use of electronic health records, including privacy, confidentiality …

Electronic informed consent criteria for research ethics review: a scoping review

MYPM Yusof, CH Teo, CJ Ng - BMC Medical Ethics, 2022 - Springer
Background The research shows a growing trend in using an electronic platform to
supplement or replace traditional paper-based informed consent processes. Instead of the …

[HTML][HTML] Implementation of electronic informed consent in biomedical research and stakeholders' perspectives: systematic review

E De Sutter, D Zaçe, S Boccia, ML Di Pietro… - Journal of medical …, 2020 - jmir.org
Background Informed consent is one of the key elements in biomedical research. The
introduction of electronic informed consent can be a way to overcome many challenges …

[HTML][HTML] Replacing paper informed consent with electronic informed consent for research in academic medical centers: a scoping review

C Chen, PI Lee, KJ Pain, D Delgado… - AMIA Summits on …, 2020 - ncbi.nlm.nih.gov
Although experts have identified benefits to replacing paper with electronic consent
(eConsent) for research, a comprehensive understanding of strategies to overcome barriers …

Virtual clinical trials: perspectives in dermatology

Z Ali, JR Zibert, SF Thomsen - Dermatology, 2020 - karger.com
Background: The cost of developing a new drug is approximately USD 2.6 billion, and over
two-thirds of the total cost is embedded in the clinical-testing phase. Patient recruitment is …

[HTML][HTML] Patient perspectives and preferences for consent in the digital health context: State-of-the-art literature review

I Kassam, D Ilkina, J Kemp, H Roble… - Journal of medical …, 2023 - jmir.org
Background The increasing integration of digital health tools into care may result in a greater
flow of personal health information (PHI) between patients and providers. Although privacy …

[HTML][HTML] Patients' and Members of the Public's Wishes Regarding Transparency in the Context of Secondary Use of Health Data: Scoping Review

A Cumyn, JF Ménard, A Barton, R Dault… - Journal of Medical …, 2023 - jmir.org
Background: Secondary use of health data has reached unequaled potential to improve
health systems governance, knowledge, and clinical care. Transparency regarding this …

E-Consent—a guide to maintain recruitment in clinical trials during the COVID-19 pandemic

R Almeida-Magana, H Maroof, J Grierson, R Clow… - Trials, 2022 - Springer
Background The COVID-19 pandemic has posed daunting challenges when conducting
clinical research. Adopting new technologies such as remote electronic consent (e-Consent) …