Towards an understanding of the ethics of electronic consent in clinical trials

被引：0
|
作者：
Sahan, Katherine [2 ]
Wijesurendra, Rohan [1 ]
Preiss, David [1 ]
Mafham, Marion [1 ]
Sheehan, Mark [2 ]
机构：
[1] Univ Oxford, Clin Trial Serv Unit, Oxford Populat Hlth, Richard Doll Bldg,Old Rd Campus,Roosevelt Dr, Oxford OX3 7LF, England
[2] Univ Oxford, Big Data Inst, Ethox Ctr, Oxford Populat Hlth, Old Rd Campus,Roosevelt Dr, Oxford OX3 7LF, England
来源：
TRIALS | 2024年 / 25卷 / 01期
关键词：
INFORMED-CONSENT; DESIGN;
D O I：
10.1186/s13063-024-08330-3
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
There are good practical reasons to use electronic consent (e-consent) in randomised trials, especially when conducting large-scale clinical trials to answer population-level health research questions. However, determining ethical reasons for e-consent is not so clear and depends on a proper understanding of what e-consent means when used in clinical trials and its ethical significance. Here we focus on four features of ethical significance which give rise to a range of ethical considerations relating to e-consent and merit further focused ethics research.
引用
收藏
页数：7
相关论文
共 50 条
  • [1] Ethics and Informed Consent for Comparative Effectiveness Research With Prospective Electronic Clinical Data
    Faden, Ruth
    Kass, Nancy
    Whicher, Danielle
    Stewart, Walter
    Tunis, Sean
    MEDICAL CARE, 2013, 51 (08) : S53 - S57
  • [2] The Ethics of Decentralized Clinical Trials and Informed Consent: Taking Technologies' Soft Impacts into Account
    van Rijssel, Tessa I.
    van Thiel, Ghislaine J. M. W.
    van Delden, Johannes J. M.
    HEALTH CARE ANALYSIS, 2025, 33 (02) : 139 - 150
  • [3] A systematic review finds underreporting of ethics approval, informed consent, and incentives in clinical trials
    Ly Quoc Trung
    Morra, Mostafa Ebraheem
    Nguyen Duc Truong
    Turk, Tarek
    Elshafie, Ahmed
    Foly, Amr
    Dao Ngoc Hien Tam
    Iraqi, Ahmed
    Trinh Thi Hong Van
    Elgebaly, Ahmed
    Tran Nhu Ngoc
    Tran Le Huy Vu
    Ngan Thy Chu
    Hirayama, Kenji
    Karbwang, Juntra
    Nguyen Tien Huy
    JOURNAL OF CLINICAL EPIDEMIOLOGY, 2017, 91 : 80 - 86
  • [4] Informed consent in clinical trials
    Verheggen, FWSM
    vanWijmen, FCB
    HEALTH POLICY, 1996, 36 (02) : 131 - 153
  • [5] CLINICAL TRIALS WITHOUT CONSENT?
    Kim, Scott Y. H.
    PERSPECTIVES IN BIOLOGY AND MEDICINE, 2016, 59 (01) : 132 - 146
  • [6] Personalized and longitudinal electronic informed consent in clinical trials: How to move the needle?
    De Sutter, Evelien
    Barbier, Liese
    Borry, Pascal
    Geerts, David
    Ioannidis, John P. A.
    Huys, Isabelle
    DIGITAL HEALTH, 2024, 10
  • [7] Ethics in clinical trials
    Rooney, Laura K.
    Serpell, Michael
    ANAESTHESIA AND INTENSIVE CARE MEDICINE, 2020, 21 (12) : 673 - 676
  • [8] Ethics and clinical trials
    Chassany, O
    Duracinsky, M
    FUNDAMENTAL & CLINICAL PHARMACOLOGY, 1999, 13 (04) : 437 - 444
  • [9] Ethics of Informed Consent for Pragmatic Trials with New Interventions
    Kalkman, Shona
    Kim, Scott Y. H.
    van Thiel, Ghislaine J. M. W.
    Grobbee, Diederick E.
    van Delden, Johannes J. M.
    VALUE IN HEALTH, 2017, 20 (07) : 902 - 908
  • [10] "Targeted" Consent for Pragmatic Clinical Trials
    David Wendler
    Journal of General Internal Medicine, 2015, 30 : 679 - 682
12345