|
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? |
07/09/2024 |
| 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 |