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Pharmaceutical Medicine|April 1, 2025
The Importance of Including Underserved Populations in ResearchKayla R Mehl, Stephanie R Morain, Emily A LargentJournal of the National Cancer Institute|May 12, 2019
Recruitment and Trial-Finding Apps-Time for Rules of the RoadStephanie R Morain, Emily A LargentThe Hastings Center Report|April 11, 2021
Public Attitudes toward Consent When Research Is Integrated into Care-Any "Ought" from All the "Is"?Stephanie R Morain, Emily A LargentLearning Health Systems|January 21, 2026
Empirical research related to the ethics of pragmatic clinical trials: A scoping reviewKayla R Mehl, Stephanie R Morain, Jeremy SugarmanJournal of the American Geriatrics Society|May 7, 2026
Designing Consent Processes for Research With Older Adults Who May Lack Decisional Capacity: A Guide for InvestigatorsEmily A Largent, Stephanie R Morain, Jason KarlawishThe American Journal of Bioethics : AJOB|April 18, 2019
When Is It Ethical for Physician-Investigators to Seek Consent From Their Own Patients?Stephanie R Morain, Steven Joffe, Emily A LargentJAMA Network Open|July 25, 2023
Physician-Investigator, Research Coordinator, and Patient Perspectives on Dual-Role Consent in Oncology: A Qualitative StudyStephanie R Morain, Dorit Barlevy, Steven Joffe, et al.Clinical Trials (London, England)|June 25, 2024
The ethical value of consulting community members in non-emergency trials conducted with waivers of informed consent for researchEmily A Largent, Steven Joffe, Neal W Dickert, et al.The Hastings Center Report|August 21, 2019
Ostriches and Obligations: Ethical Challenges Facing Research on Usual CareStephanie R MorainThe Hastings Center Report|October 13, 2018
Whom to Engage in Patient-Engaged Research? Reflection on SelectionStephanie R MorainPageof 14