[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"detail-sidebar-cat-0-en-105":3,"doc-seo-430311-105":59,"doc-detail-430311-en":130},{"code":4,"msg":5,"data":6},0,"success",[7,13,18,23,28,33,38,43,48,51,55],{"id":8,"doc_module":4,"doc_module_name":9,"category_name":10,"show_sort_weight":11,"slug":12},1,"Document","Story & Novel",90,"story-novel",{"id":14,"doc_module":4,"doc_module_name":9,"category_name":15,"show_sort_weight":16,"slug":17},2,"Literature",80,"literature",{"id":19,"doc_module":4,"doc_module_name":9,"category_name":20,"show_sort_weight":21,"slug":22},4,"Exam",70,"exam",{"id":24,"doc_module":4,"doc_module_name":9,"category_name":25,"show_sort_weight":26,"slug":27},5,"Comic",60,"comic",{"id":29,"doc_module":4,"doc_module_name":9,"category_name":30,"show_sort_weight":31,"slug":32},6,"Technology",50,"technology",{"id":34,"doc_module":4,"doc_module_name":9,"category_name":35,"show_sort_weight":36,"slug":37},7,"Healthcare",40,"healthcare",{"id":39,"doc_module":4,"doc_module_name":9,"category_name":40,"show_sort_weight":41,"slug":42},8,"Research & Report",30,"research-report",{"id":44,"doc_module":4,"doc_module_name":9,"category_name":45,"show_sort_weight":46,"slug":47},9,"Religion & Spirituality",20,"religion-spirituality",{"id":46,"doc_module":4,"doc_module_name":9,"category_name":49,"show_sort_weight":46,"slug":50},"World Cup","world-cup",{"id":52,"doc_module":4,"doc_module_name":9,"category_name":53,"show_sort_weight":52,"slug":54},10,"Lifestyle","lifestyle",{"id":56,"doc_module":4,"doc_module_name":9,"category_name":57,"show_sort_weight":24,"slug":58},19,"General","general",{"code":4,"msg":60,"data":61},"ok",{"site_id":62,"language":63,"slug":64,"title":65,"keywords":66,"description":67,"schema_data":68,"social_meta":123,"head_meta":125,"extra_data":127,"updated_unix":129},105,"en","informed-consent-document-template-research-participation","Informed Consent Document Template - Research Participation","","Provides a researcher-focused informed consent document template and guidance for preparing consent materials for Institutional Review Board (IRB) review. Includes instructions to keep section headings intact, remove italic explanatory text, and provide a plain-language concise summary covering study purpose, procedures, time commitment, risks, and potential benefits. Supplies detailed consent sections on project nature and purpose, invitation rationale, study requirements, risks/discomforts, benefits, confidentiality/anonymity, future use of identifiable data under the Revised Common Rule, and compensation, refusal/withdrawal, and contact information.",{"@graph":69,"@context":122},[70,84,105],{"@type":71,"itemListElement":72},"BreadcrumbList",[73,77,79,82],{"item":74,"name":75,"@type":76,"position":8},"https://docshare.wps.com","Home","ListItem",{"item":78,"name":9,"@type":76,"position":14},"https://docshare.wps.com/document/",{"item":80,"name":35,"@type":76,"position":81},"https://docshare.wps.com/document/healthcare/",3,{"item":83,"name":65,"@type":76,"position":19},"https://docshare.wps.com/document/informed-consent-document-template-research-participation/430311/",{"url":83,"name":65,"@type":85,"image":86,"author":91,"headline":65,"publisher":94,"fileFormat":97,"inLanguage":63,"description":67,"dateModified":98,"datePublished":99,"encodingFormat":97,"isAccessibleForFree":100,"interactionStatistic":101},"DigitalDocument",{"url":87,"@type":88,"width":89,"height":90},"https://docshare.wps.com/thumbnails/informed-consent-document-template-research-participation/430311.png","ImageObject",300,407,{"name":92,"@type":93},"Angel","Person",{"url":74,"name":95,"@type":96},"DocShare","Organization","application/vnd.openxmlformats-officedocument.wordprocessingml.document","2026-10-31","2026-09-29",true,{"@type":102,"interactionType":103,"userInteractionCount":44},"InteractionCounter",{"@type":104},"ViewAction",{"@type":106,"mainEntity":107},"FAQPage",[108,114,118],{"name":109,"@type":110,"acceptedAnswer":111},"What information must be included in the concise summary at the start of the informed consent document?","Question",{"text":112,"@type":113},"It must include the investigator’s name, the study purpose, what participation involves, anticipated risks, and the estimated time to complete the study, all in non-technical language.","Answer",{"name":115,"@type":110,"acceptedAnswer":116},"What should researchers do with italic text and section headings in the template?",{"text":117,"@type":113},"Italic text is intended to explain elements of the consent and should be deleted from materials submitted. Section headings should be left intact to help participants understand each section’s content.",{"name":119,"@type":110,"acceptedAnswer":120},"How should confidentiality and future use of data be addressed under the Revised Common Rule?",{"text":121,"@type":113},"If identifiable information is collected, the consent must directly address potential future usage by including one of two statements: de-identified information may be used for future research without additional consent, or it will not be used or distributed for future research even if identifiers are removed.","https://schema.org",{"og:url":83,"og:type":124,"og:title":65,"og:site_name":95,"og:description":67},"article",{"robots":126,"canonical":83},"index,follow",{"doc_id":128,"site_id":62},430311,1791394804,{"code":4,"msg":5,"data":131},{"doc_id":128,"user_id":132,"nickname":92,"user_avatar":133,"doc_module":4,"category_id":34,"category_name":35,"doc_title":65,"doc_description":67,"doc_content":134,"file_id":135,"file_url":136,"file_type":137,"file_size":138,"view_count":44,"is_deleted":4,"is_public":8,"is_downloadable":8,"audit_status":8,"page_count":29,"language":139,"language_code":63,"site_id":62,"html_lang":63,"table_of_contents":140,"faqs":141,"seo_title":142,"seo_description":67,"update_tm":143,"read_time":144,"preview_page_count":4},687207412472,"https://ap-avatar.wpscdn.com/davatar_155a257f0dc6eb9ab79c44ca47cae57d","The following material is provided as an aid to researchers in constructing your informed consent document.  It is strongly suggested that you use the recommended language below, inserting study-specific details as appropriate where we have provided [bracketed text].  This will allow for a more rapid review of your materials.  Similarly, we would recommend that you leave the section headings (e.g., “Nature and Purpose of the Project”) intact, because those make it easier for participants to understand the sections of the consent document and what information is contained within each. Any text presented in italics is intended to explain elements of the consent document to you as the researcher, and should be deleted from materials submitted to our office.\nINFORMED CONSENT DOCUMENT TEMPLATE\nA concise summary should be provided first.  It must contain the following information in non-technical language:\nYour name; a description of the purpose of the study; what participating in the study involves; what the anticipated risks of participation are; how long it will take to complete the study:\nMy name is [name of PI] and you are being given the opportunity to volunteer to participate in a project conducted through Xavier University [and, if applicable, any other co-operating institution]. The purpose of this study is [brief statement of purpose]. Participants in this study will be asked to [describe the elements of the study in non-technical language].  The study should take [time estimate, allowing for individual differences as appropriate] for you to complete.  Risks related to participation include [list any anticipated risks; if none are anticipated, stating that there are no anticipated risks is acceptable].  Benefits to taking part include [provide an overview of direct and indirect benefits; note that compensation, including research participation credit, is NOT considered a “benefit” of participating].\nIn the following sections, provide more information and detail as appropriate.\nNature and Purpose of the Project\n[Re-state and, as needed, expand upon the nature and purpose of the project as presented in the concise summary.  If the study involves a manipulation that is not being revealed AND seeks Exempt-status review, participants must be informed that they may be deceived or incompletely informed about the purpose of the study; this does not have to be revealed if the study will be reviewed under the Expedited or Full Board category.]\nWhy You Were Invited to Take Part\n[Provide brief information about why the individual reading the consent form was asked to take part in the study.]\nStudy Requirements\n[Re-state and, as needed, expand upon the study requirements as presented in the concise summary.]\nAnticipated discomforts/risks\n[Re-state and, as needed, expand upon the anticipated discomforts and risks as presented in the concise summary.]\nBenefits\n[Re-state and, as needed, expand upon the potential direct and indirect benefits as presented in the concise summary.]\nConfidentiality/Anonymity\n[If the study will collect participant identifiers, then participation is confidential rather than anonymous.  For confidential studies, explain how privacy will be maintained, if and when identifying information will be removed from the data file, how data will be stored, and when it will be destroyed.  Explain the legal limits of confidentiality as they apply to the study.  If the study will NEVER collect participant identifiers, participants should be informed that data will be collected anonymously and that therefore, their answers can never be linked to them.]\n[IMPORTANT NOTE: In the Revised Common Rule (effective January 2019), if you collect identifiable information, you MUST directly address the potential for future usage of the data collected.  If you collect identifiable information, one of the two following statements must be included:\nPersonal identifiers may be removed, and the de-identified information may be used for future ","cbCaiik3kOJM65ZI","https://ap.wps.com/l/cbCaiik3kOJM65ZI","docx",21302,"English","# Informed Consent Document Template\n## Concise Summary Requirements\n## Nature and Purpose of the Project\n## Why You Were Invited to Take Part\n## Study Requirements\n## Anticipated Discomforts/Risks\n## Benefits\n## Confidentiality/Anonymity\n## Compensation\n## Refusal, Withdrawal, and Questions/Contacts\n## Signature and Dates","[{\"question\":\"What information must be included in the concise summary at the start of the informed consent document?\",\"answer\":\"It must include the investigator’s name, the study purpose, what participation involves, anticipated risks, and the estimated time to complete the study, all in non-technical language.\"},{\"question\":\"What should researchers do with italic text and section headings in the template?\",\"answer\":\"Italic text is intended to explain elements of the consent and should be deleted from materials submitted. Section headings should be left intact to help participants understand each section’s content.\"},{\"question\":\"How should confidentiality and future use of data be addressed under the Revised Common Rule?\",\"answer\":\"If identifiable information is collected, the consent must directly address potential future usage by including one of two statements: de-identified information may be used for future research without additional consent, or it will not be used or distributed for future research even if identifiers are removed.\"}]","Informed Consent Document Template - Research Participation | DOCX",1790652510,15]