Making clinical trials more patient-centered using digital interactive e-consent tools

Making clinical trials more patient-centered using digital interactive e-consent tools
Author :
Publisher : RTI Press
Total Pages : 10
Release :
ISBN-10 :
ISBN-13 :
Rating : 4/5 ( Downloads)

Book Synopsis Making clinical trials more patient-centered using digital interactive e-consent tools by : Barbara Bowles Biesecker

Download or read book Making clinical trials more patient-centered using digital interactive e-consent tools written by Barbara Bowles Biesecker and published by RTI Press. This book was released on 2019-10-20 with total page 10 pages. Available in PDF, EPUB and Kindle. Book excerpt: Research participants are required to give their consent to participate in clinical trials and nonexempt government-funded studies. The goal is to facilitate participant understanding of the intent of the research, its voluntary nature, and the potential benefits and harms. Ideally, participants make an informed choice whether to participate; one that is based on having sufficient relevant knowledge and that is consistent with their values and preferences. Achieving this objective can be challenging, and as such, many scholars have declared the consent process flawed or “broken.” Moreover, clinical trials are complex studies, and compelling evidence suggests that current consent processes are inadequate in achieving informed choice. E-consent offers a dynamic, engaging consent delivery mode that can effectively support making informed decisions about whether to participate in a trial.


Making clinical trials more patient-centered using digital interactive e-consent tools Related Books

Making clinical trials more patient-centered using digital interactive e-consent tools
Language: en
Pages: 10
Authors: Barbara Bowles Biesecker
Categories: Medical
Type: BOOK - Published: 2019-10-20 - Publisher: RTI Press

DOWNLOAD EBOOK

Research participants are required to give their consent to participate in clinical trials and nonexempt government-funded studies. The goal is to facilitate pa
Making Clinical Trials More Patient-centered Using Digital Interactive E-consent Tools
Language: en
Pages: 5
Authors: Barbara Biesecker
Categories: Informed consent (Medical law)
Type: BOOK - Published: 2019 - Publisher:

DOWNLOAD EBOOK

Research participants are required to give their consent to participate in clinical trials and nonexempt government-funded studies. The goal is to facilitate pa
Report of the International Bioethics Committee of UNESCO (IBC) on Social Responsibility and Health
Language: en
Pages: 69
Authors: UNESCO
Categories: Bioethics
Type: BOOK - Published: 2010 - Publisher: UNESCO

DOWNLOAD EBOOK

Virtual Clinical Trials
Language: en
Pages: 127
Authors: National Academies of Sciences, Engineering, and Medicine
Categories: Medical
Type: BOOK - Published: 2019-11-16 - Publisher: National Academies Press

DOWNLOAD EBOOK

Successful drug development relies on accurate and efficient clinical trials to deliver the best and most effective pharmaceuticals and clinical care to patient
Additional Protocol to the Convention on Human Rights and Biomedicine, Concerning Biomedical Research
Language: en
Pages: 32
Authors: Council of Europe
Categories: Political Science
Type: BOOK - Published: 2005-01-01 - Publisher: Council of Europe

DOWNLOAD EBOOK

This protocol covers the full range of research activities in the health field that involve interventions on human beings. It aims to protect the dignity and id