about
Clinical trials and medical care: defining the therapeutic misconceptionInformed consent for comparative effectiveness trialsThe value of unhealthy eating and the ethics of healthy eating policiesThe views of quality improvement professionals and comparative effectiveness researchers on ethics, IRBs, and oversightStakeholders' Views of Alternatives to Prospective Informed Consent for Minimal-Risk Pragmatic Comparative Effectiveness TrialsAn ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethicsThe research-treatment distinction: a problematic approach for determining which activities should have ethical oversightThe OHRP and SUPPORTEthics and informed consent for comparative effectiveness research with prospective electronic clinical dataInformed consent, comparative effectiveness, and learning health careChallenges for mental health services raised by disaster preparedness: mapping the ethical and therapeutic terrain.Ethics and severe pandemic influenza: maintaining essential functions through a fair and considered response.An ethics framework for public health and avian influenza pandemic preparedness.Public health ethics: mapping the terrain.Outcome of a research ethics training workshop among clinicians and scientists in a Nigerian university.Toward a more comprehensive approach to protecting human subjects: the interface of data safety monitoring boards and institutional review boards in randomized clinical trials.Post-consent assessment of dental subjects' understanding of informed consent in oral health research in Nigeria.Community engagement strategies in the original and renewal applications for CTSA grant funding.Purpose and benefits of early phase cancer trials: what do oncologists say? What do patients hear?An intervention to improve cancer patients' understanding of early-phase clinical trials.Research Ethics Consultation at the Johns Hopkins Bloomberg School of Public Health.A comparison of online versus on-site training in health research methodology: a randomized studyAccess to treatment in HIV prevention trials: perspectives from a South African community.Repeated assessments of informed consent comprehension among HIV-infected participants of a three-year clinical trial in Botswana.The ethics of health systems research in low- and middle-income countries: a call to action.Are research subjects adequately protected? A review and discussion of studies conducted by the Advisory Committee on Human Radiation Experiments.Human rights, politics, and reviews of research ethics.Evaluating international research ethics capacity development: an empirical approach.Research ethics capacity building in Sub-Saharan Africa: a review of NIH Fogarty-funded programs 2000–2012.The informed consent process in a rural African setting: a case study of the Kassena-Nankana district of Northern Ghana.Motivations, understanding, and voluntariness in international randomized trials.Rapid estimate of adult literacy in medicine: feasible by telephone?The use of CT for screening: a national survey of radiologists' activities and attitudesOur two cents: research ethics consultation at Johns Hopkins Bloomberg School of Public Health.Screening in the dark: ethical considerations of providing screening tests to individuals when evidence is insufficient to support screening populationsFaculty perspectives on community-based research: "I see this still as a journey".Assessing the readability of non-English-language consent forms: the case of Kiswahili for research conducted in Kenya.A pilot study of simple interventions to improve informed consent in clinical research: feasibility, approach, and resultsEthical oversight of research in developing countries.Understanding the supports of and challenges to community engagement in the CTSAs.
P50
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