  {"id":4386,"date":"2024-01-08T13:18:46","date_gmt":"2024-01-08T18:18:46","guid":{"rendered":"https:\/\/www.rochester.edu\/ohsp\/?page_id=4386"},"modified":"2024-03-20T15:35:13","modified_gmt":"2024-03-20T19:35:13","slug":"consent","status":"publish","type":"page","link":"https:\/\/www.rochester.edu\/ohsp\/resources\/consent\/","title":{"rendered":"Informed Consent"},"content":{"rendered":"<p>A critical requirement for conducting ethical research is obtaining voluntary, informed consent from subjects. Informed consent is an information exchange process that takes place between a potential subject and the study team, which begins when the subject first learns about the research and continues throughout the course of the study. These resources will help you ensure proper processes for informed consent throughout the human research process.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>A critical requirement for conducting ethical research is obtaining voluntary, informed consent from subjects. Informed consent is an information exchange process that takes place between a potential subject and the&hellip;<\/p>\n","protected":false},"author":36,"featured_media":0,"parent":236,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":"","_members_access_role":[],"_members_access_error":""},"class_list":["post-4386","page","type-page","status-publish","hentry"],"acf":{"lead_in":"","display_title":"","subtitle":"","call_to_action":"","hero_image_placement":"no_image","hero_media":"images","hero_pattern_option":"","hero_video":"","hero_image_landing":"","hero_image_landing_two":"","hero_image_landing_three":"","content_modules":[{"acf_fc_layout":"card_grid","anchor":"","css_class":"","title":"","description":"","background_color":"#FFFFFF","width":"width-large","columns":"3","cards":[{"card_title":"<h5>OHSP Policy 701: Informed Consent<\/h5>","card_text":"Reference and download the full formal policy 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research","card_background_color":"#f4f4f4","card_hover_color":"#283faf","card_link":{"title":"Templates","url":"https:\/\/www.rochester.edu\/ohsp\/templates\/#consent","target":""},"card_hover_arrow":"hover_arrow","card_image":"","card_image_size":"","card_image_placement":"","card_image_hover_state":"hover_fade","card_image_link":""},{"card_title":"<h5>'Key information' requirements<\/h5>","card_text":"Understand what 'key information' needs to be included at the start of your consent form","card_background_color":"#f4f4f4","card_hover_color":"#283faf","card_link":{"title":"Key Information","url":"https:\/\/www.rochester.edu\/ohsp\/resources\/consent\/key-information\/","target":""},"card_hover_arrow":"hover_arrow","card_image":"","card_image_size":"","card_image_placement":"","card_image_hover_state":"hover_fade","card_image_link":""},{"card_title":"<h5>Documentation of consent<\/h5>","card_text":"Learn how to document consent in manners that meet legal requirements","card_background_color":"#f4f4f4","card_hover_color":"#283faf","card_link":{"title":"Documentation","url":"https:\/\/www.rochester.edu\/ohsp\/resources\/consent\/documentation\/","target":""},"card_hover_arrow":"hover_arrow","card_image":"","card_image_size":"","card_image_placement":"","card_image_hover_state":"hover_fade","card_image_link":""},{"card_title":"<h5>Re-consent<\/h5>","card_text":"Ongoing research may require re-consent of subjects to maintain compliance","card_background_color":"#f4f4f4","card_hover_color":"#283faf","card_link":{"title":"Re-Consent","url":"https:\/\/www.rochester.edu\/ohsp\/resources\/consent\/re-consent\/","target":""},"card_hover_arrow":"hover_arrow","card_image":"","card_image_size":"","card_image_placement":"","card_image_hover_state":"hover_fade","card_image_link":""},{"card_title":"<h5>Remote consent<\/h5>","card_text":"Learn how to ensure that subjects' privacy and confidentiality is upheld when remotely gaining consent","card_background_color":"#f4f4f4","card_hover_color":"#283faf","card_link":{"title":"Remote Consent","url":"https:\/\/www.rochester.edu\/ohsp\/resources\/consent\/remote\/","target":""},"card_hover_arrow":"hover_arrow","card_image":"","card_image_size":"","card_image_placement":"","card_image_hover_state":"hover_fade","card_image_link":""},{"card_title":"<h5>Enrolling Non-English Speaking Subjects<\/h5>","card_text":"Review considerations and methods for enrolling non-English speaking subjects","card_background_color":"#f4f4f4","card_hover_color":"#283faf","card_link":{"title":"Enrolling Non-English Speaking Subjects","url":"https:\/\/www.rochester.edu\/ohsp\/resources\/non-english-speaking-subjects\/","target":""},"card_hover_arrow":"hover_arrow","card_image":"","card_image_size":"","card_image_placement":"","card_image_hover_state":"hover_fade","card_image_link":""},{"card_title":"<h5>Subject Screening<\/h5>","card_text":"Learn how screening provisions impact the consent process.","card_background_color":"#f4f4f4","card_hover_color":"#283faf","card_link":{"title":"Subject Screening","url":"https:\/\/www.rochester.edu\/ohsp\/resources\/subject-screening\/","target":""},"card_hover_arrow":"hover_arrow","card_image":"","card_image_size":"","card_image_placement":"","card_image_hover_state":"hover_fade","card_image_link":""}]}]},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Informed Consent - Office for Human Subject Protection - 糖心传媒<\/title>\n<meta name=\"description\" content=\"Explore consent-related resources to ensure human subject research is conducted correctly. 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