Standardized Text for Informed Consent Forms Last Update Blood draw risk 04/24/2007 Certificates of Confidentiality 11/29/2017 Clinicaltrials.gov language 05/15/2012 Genetic Information Nondiscrimination Act (GINA) 11/05/2021 NIH GDS_GWAS consent addendum 02/06/2023 Internet Search Language 03/04/2015 LAR Addendum: Risk for Loss of Capacity 03/18/2016 Magnetic resonance imaging 04/24/2007 NIH DMS Consent Addendum 1/25/2023 Placebo/Randomization 04/24/2007 Phase I study benefit language (Question 11.a.) 05/22/2012 If you choose to take part in this study, will it cost you anything? 12/21/2016 Will you be paid for taking part in this study? 08/26/2021 What if you are injured because of the study? 03/01/2024 Radiation 06/06/2008 Reading Exception Language (put in Question 7 of the Informed Consent). 09/10/2010 New template Recording Subjects: photographs, video recordings, and/or audio recordings 09/01/23 Reproductive Risks (pregnancy) 06/20/2008 Storage of Tissue 05/17/2013 Storage of Tissue (sIRB studies) 11/13/2020 Student Subjects 04/24/2007 Study Subject Return to Research Template 05/18/2020 You/Your Child box templates 05/15/2012 VA EFT Compensation 09/21/2018 “Waiver of Documentation of Informed Consent” Sample Letter 04/04/2013