Personalized and long-term electronic informed consent in clinical research: stakeholder views
暂无分享,去创建一个
[1] P. Valcke,et al. Conducting Non-COVID-19 Clinical Trials during the Pandemic: Can Today's Learning Impact Framework Efficiency? , 2020, European journal of health law.
[2] I. Huys,et al. Implementation of Electronic Informed Consent in Biomedical Research and Stakeholders’ Perspectives: Systematic Review , 2020, Journal of medical Internet research.
[3] K. Nilsson,et al. Patients’ reasoning regarding the decision to participate in clinical cancer trials: an interview study , 2018, Trials.
[4] Michael Goldsmith,et al. Wider Research Applications of Dynamic Consent , 2018, Privacy and Identity Management.
[5] S. R. Ramos,et al. User-Centered Design, Experience, and Usability of an Electronic Consent User Interface to Facilitate Informed Decision-Making in an HIV Clinic , 2017, Computers, informatics, nursing : CIN.
[6] R. Kadam. Informed consent process: A step further towards making it meaningful! , 2017, Perspectives in clinical research.
[7] S. Beck,et al. Dynamic Consent: a potential solution to some of the challenges of modern biomedical research , 2017, BMC Medical Ethics.
[8] J. Perlmutter,et al. Paving the way to a more effective informed consent process: Recommendations from the Clinical Trials Transformation Initiative. , 2016, Contemporary clinical trials.
[9] Ellen Uiters,et al. Health literacy in Europe: comparative results of the European health literacy survey (HLS-EU) , 2015, European journal of public health.
[10] Michael Morrison,et al. Dynamic consent: a patient interface for twenty-first century research networks , 2014, European Journal of Human Genetics.
[11] N. Gale,et al. Using the framework method for the analysis of qualitative data in multi-disciplinary health research , 2013, BMC Medical Research Methodology.
[12] Adam A. Nishimura,et al. Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trials , 2013, BMC medical ethics.
[13] V. Entwistle,et al. Supporting positive experiences and sustained participation in clinical trials: looking beyond information provision , 2012, Journal of Medical Ethics.
[14] D. Resnik,et al. Participants’ responsibilities in clinical research , 2012, Journal of Medical Ethics.
[15] Matthew E Falagas,et al. Informed consent: how much and what do patients understand? , 2009, American journal of surgery.
[16] P. Sainsbury,et al. Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups. , 2007, International journal for quality in health care : journal of the International Society for Quality in Health Care.
[17] V. Jenkins,et al. Reasons for accepting or declining to participate in randomized clinical trials for cancer therapy , 2000, British Journal of Cancer.
[18] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..