Table of Contents:
- e-Consent: A Key Advancement in Clinical Research and Digital Health
1.1. Electronic Informed Consent: Definition
1.2. Informed Consent in Medical Research and Ethics
1.3. Moving from Paper-based Informed Consent to Digital Consent
1.4. Benefits of Electronic Informed Consent
- Digital Consent Design and Bioethics
- Types of Digital Consent Forms and e-Consent Systems
- Electronic Informed Consent and Multimedia Tools
- Teleconsent, Electronic Signatures, and Clinical Trials
- Digital Consent, Electronic Health Records, and Patient Preferences
- Self-administered Electronic Informed Consent and Patient-centered Research
- Digital Consent and Interoperability between Legacy Systems
- Electronic Informed Consent in Prospective Cohort Studies and Follow-ups
- Digital Consent: Conclusion
- Resources