Although exempt research is exempt from some of the federal regulations, in most cases of interaction with participants, a consent process is indicated. It’s important to understand that even though ...
It can be a rewarding experience to participate in research studies that offer many potential personal, medical, and financial benefits. However, if you are new to or are not entirely familiar with ...
Informed consent is one of the most important aspects of conducting ethical research with human participants. Respecting the autonomy of research participants, the investigator must provide complete ...
Consent forms that people sign before participating in research are widely considered difficult to understand and sometimes inaccurate. Lack of clarity was implicated in a high-profile legal ...
On March 1, 2024, the U.S. Food and Drug Administration (FDA) and the U.S. Department of Health and Human Services’ (HHS’s) Office for Human Research Protections (OHRP) released a draft guidance ...
Abbreviations: CCRI, Capacity to Consent to Research Instrument; MG, malignant gliomas V; SD, standard deviation; HVLT, Hopkins Verbal Learning Test; CFL, controlled oral word association test; ...
The aims of this study were to determine which consent procedure patients prefer for use of stored tissue for research purposes and what the effects of consent procedures on actual consenting ...
When submitting a project through the eIRB system, researchers can request either a waiver of the need for signatures/documentation, or a waiver to alter or omit the entire consent process. In either ...
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