Did you know that most of your research subjects are reading at the 8th-grade level or lower? Learn how to write the simplest, clearest consent forms, so that every one of your subjects can be fully informed. This workshop will teach you specific skills for writing easy-to-understand documents. The learning objectives of this session are for participants to understand the elements of consent, acquire plain language tips for editing research consent forms, and identify which Partners consent form template is appropriate for your protocol.
This session is limited to 25 participants to facilitate interaction.
Registration is required. Please contact Tiereny Morrison-Rohlfs at tmorrison-rohlfs@partners.org with any questions.
Programs: Beginner Clinical Research Coordinator Clinical Research Investigator Experienced Clinical Research Coordinator
Categories: Clinical Research Ethical Oversight IRB
Sponsor: MGH Division of Clinical Research
Modules
IRB Roundtable: Consent Form Writing |
Past Offerings
IRB Roundtable: Consent Form Writing | Dec. 14, 2017 |
IRB Roundtable: Consent Form Writing | Dec. 1, 2016 |
IRB Roundtable: Consent Form Writing | Nov. 8, 2018 |
IRB Roundtable: Consent Form Writing | Nov. 14, 2019 |
Reviews
Date Reviewed: Jan. 21, 2020, 12:17 p.m.
Date Reviewed: Nov. 9, 2018, 2:01 p.m.
Date Reviewed: Nov. 8, 2018, 12:48 p.m.
Date Reviewed: Dec. 14, 2017, 2:20 p.m.