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Respect Tribal Sovereignty in Indigenous Research
In what may help overcome a history of well-earned distrust by indigenous people, a research collaborative has developed a curriculum to teach IRB members and others the distinct cultural issues that arise in studying Native Americans.
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Unique Informed Consent Challenges if Research Participant Is Incarcerated
It is well-established that incarcerated people suffer disproportionately from low literacy and health-related conditions that can affect cognition. Despite this, modified informed consent processes are not required by federal guidelines.
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Ethical Challenges of Social Research in the Digital Age
As we leave the analog age and enter the vast expanse of digital “big data,” the potential benefits and risks for social science research are uncharted. However, this bright future casts a shadow as big data raises the specter of ethical breaches of informed consent and violated privacy.
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Create More Thorough, Efficient New IRB Member Training
Educating and onboarding IRB members should include more than perfunctory online human subjects research training. The goal could be to provide new members with comprehensive information in a well-organized training program.
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Low Health Numeracy Also Is an Informed Consent Problem
Low health numeracy is a problem that could affect how well trials recruit and provide informed consent to potential participants. It’s defined by how well people access, process, interpret, communicate, and act on numerical, biostatistical, and other numbers-related health information.
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Tips for Simplifying Informed Consent Language
Using plain language in informed consent forms means exchanging medical and statistical jargon for words that people with low health literacy and low health numeracy would understand.
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Give People What They Need in Informed Consent: Plain Language
Most research informed consent forms are written at a high school reading level when many people who are being recruited for studies might need language nearer to a fifth-grade level, according to a new study.
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Dissenting Opinion: New Common Rule Penalizes the Compliant
Many see the single IRB requirement in the revised Common Rule as a necessary sword to sever the Gordian knot of regulatory overlap and unnecessary delay of multisite review. Suzanne M. Rivera, PhD, is not one of them.
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Deadline Extended for Common Rule Compliance
With finalization of the revised Common Rule postponed for at least six months — and possibly one year — IRBs should continue preparing to comply with the regulation as they await additional clarification and guidance.
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Study: Pain Research Can Harm Participants
Researchers must pay greater attention to the rights of study participants in pain research, concludes a recent paper by the Ethics Committee of the Pain-Omics Group.