{"id":58503,"date":"2013-08-01T18:33:18","date_gmt":"2013-08-01T22:33:18","guid":{"rendered":"https:\/\/rarediseases.org\/informed-consent-in-biobank-research\/"},"modified":"2013-08-01T18:33:18","modified_gmt":"2013-08-01T22:33:18","slug":"informed-consent-in-biobank-research","status":"publish","type":"post","link":"https:\/\/rarediseases.org\/es\/informed-consent-in-biobank-research\/","title":{"rendered":"Informed Consent in Biobank Research"},"content":{"rendered":"<p>Genetic biobanks, storage facilities for DNA, genetic data and tissue samples, are becoming more prevalent in the rare disease community.\u00a0\u00a0 The information and samples can be made available to approved researchers for clinical studies, but unlike clinical trials, there is usually no personal benefit or follow-up provided to participants.\u00a0<!--more--> New models for biobank research have altered this paradigm, however, and may include the possibility of contacting participants with information that could be relevant to their healthcare.<\/p>\n<p>The cornerstone of ethical genetics research using data from biobanks is a proper informed consent process that ensures patients and parents understand the potential advantages, limitations, and risks of participation.\u00a0 <a title=\"NCBI\" href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/23807615\" target=\"_blank\" rel=\"noopener nofollow\">A recent study<\/a> found that parents who consented for their child\u2019s participation in a biobank for congenital cardiovascular malformations did not understand the fine details of how their child\u2019s samples would be used and stored.\u00a0 Although most parents did understand that participation was voluntary and for research, many thought that the intention was to treat their child\u2019s heart defect.\u00a0 There was also lack of understanding that their child\u2019s DNA would be stored indefinitely.<\/p>\n<p>Researchers are exploring the use of visual aids and other communications tools to try to improve understanding and obtain true informed consent.\u00a0 These methods have not been extensively studied in biobanking consent, but clearly there is a need to investigate alternatives to the standard written informed consent form.<\/p>\n<p>Have you consented to participation in a biobank for yourself or your child?<\/p>\n<p>What was the process and how do you think it could be improved?<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Genetic biobanks, storage facilities for DNA, genetic data and tissue samples, are becoming more prevalent in the rare disease community.\u00a0\u00a0 The information and samples can be made available to approved &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/rarediseases.org\/es\/informed-consent-in-biobank-research\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Informed Consent in Biobank Research&#8221;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","_price":"","_stock":"","_tribe_ticket_header":"","_tribe_default_ticket_provider":"","_tribe_ticket_capacity":"","_ticket_start_date":"","_ticket_end_date":"","_tribe_ticket_show_description":"","_tribe_ticket_show_not_going":false,"_tribe_ticket_use_global_stock":"","_tribe_ticket_global_stock_level":"","_global_stock_mode":"","_global_stock_cap":"","_tribe_rsvp_for_event":"","_tribe_ticket_going_count":"","_tribe_ticket_not_going_count":"","_tribe_tickets_list":"[]","_tribe_ticket_has_attendee_info_fields":false,"footnotes":""},"categories":[191,192,193],"tags":[294,264,295,296,208,226],"class_list":["post-58503","post","type-post","status-publish","format-standard","hentry","category-medical","category-patients-members","category-research","tag-biobank","tag-dna","tag-genetic-biobanks","tag-informed-conset","tag-marsha-lanes","tag-patients"],"acf":[],"_links":{"self":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58503","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/comments?post=58503"}],"version-history":[{"count":0,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/posts\/58503\/revisions"}],"wp:attachment":[{"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/media?parent=58503"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/categories?post=58503"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/rarediseases.org\/es\/wp-json\/wp\/v2\/tags?post=58503"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}