Having studied informed-consent forms for over a decade, I can state unequivocally that the problem of “unreadable” informed-consent forms extends well beyond the confines of research ...

Informed consent is more than just a form; it is a process that actively involves the participant. It is an "ongoing exchange of information between the investigator and [participant]" per the OHRP.

The patient stays informed about the condition and its treatment. It makes the patient use the information to take a better decision or choice. The consent form contains all the information based ...

Informed consent is an agreement between the investigators and the research participants. A signed informed consent form notifies potential research participants of their obligations and rights, and ...

A systematic analysis of 124 informed-consent documents for U.S. government-sponsored, multinational HIV/AIDS research conducted in 2006 revealed that the forms spanned more than 20 pages ...

The authors explain that oral clinical trial information is provided to patients by physicians and research nurses, but that written informed consent forms are typically developed by study ...

as well as its informed consent forms, contain the necessary information to enable a patient, or his or her representative, to make fully-informed decisions about their care, including the right ...

Informed consent may be the biggest misnomer in medicine: Studies show that most patients don't read the forms they sign before undergoing surgery or medical treatment. More than half of those who ...

Though informed consent often evokes images of thick packets of forms, the process is much broader than that and starts long before it’s time to read the fine print, Agu said. “The FDA ...

You're required to have all participants in your study complete an Informed Consent Form. See an example of an Informed Consent Form (pdf). Below are the Bethel University Institutional Review Board’s ...