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.

Moreover, the informed consent should not merely be a list of isolated facts. Many consent forms are not as good as they could be in terms of aiding decision-making. The goal is to help people process ...

The Informed Consent Form should be in the primary language of the research ... vulnerable populations or complex interventions. You may use this sample tempate to get started.

Use short paragraphs, bullets and subheadings to increase readability. See the informed consent form template (pdf) for more help and sample language. 1. Title of the Study 2. Names and Affiliations ...

This UB CTSI Educational Modules video: Defines informed consent Outlines where to find the most up-to-date consent form template, the HRP-502 Identifies the parts of the Informed Consent form Shares ...

Informed consent forms and scripts should be written at an eighth-grade reading level to ensure that prospective subjects are truly informed. See the Informed Consent Template for an example of ...

The IRB determines, for each protocol it reviews, which of the following elements and disclosures must be included in the informed ... in the form of a letter signed by the sponsor(s) with the same ...

This Informed Consent for Telehealth Sessions contains important information focusing on doing psychotherapy and advocacy using internet-based video sessions. Please ...

A single sample can yield a lot of information, but many are advocating for a change in the framework of informed consent for biomedical research to protect patients from surprises about where that ...

Investigators may request a waiver or alteration of the informed consent process or waiver of consent documentation, provided the conditions described on the waiver form are fulfilled.