[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"detail-sidebar-cat-1-en-105":3,"doc-seo-244746-105":53,"doc-detail-244746-en":127},{"code":4,"msg":5,"data":6},0,"success",[7,14,19,24,29,34,39,44,49],{"id":8,"doc_module":9,"doc_module_name":10,"category_name":11,"show_sort_weight":12,"slug":13},11,1,"Template","Presentations",90,"presentations",{"id":15,"doc_module":9,"doc_module_name":10,"category_name":16,"show_sort_weight":17,"slug":18},12,"Resumes",80,"resumes",{"id":20,"doc_module":9,"doc_module_name":10,"category_name":21,"show_sort_weight":22,"slug":23},14,"Invoices",70,"invoices",{"id":25,"doc_module":9,"doc_module_name":10,"category_name":26,"show_sort_weight":27,"slug":28},15,"Posters",60,"posters",{"id":30,"doc_module":9,"doc_module_name":10,"category_name":31,"show_sort_weight":32,"slug":33},16,"Social Media",50,"social-media",{"id":35,"doc_module":9,"doc_module_name":10,"category_name":36,"show_sort_weight":37,"slug":38},17,"Forms",40,"forms",{"id":40,"doc_module":9,"doc_module_name":10,"category_name":41,"show_sort_weight":42,"slug":43},18,"Letters",30,"letters",{"id":45,"doc_module":9,"doc_module_name":10,"category_name":46,"show_sort_weight":47,"slug":48},21,"Paper Templates",5,"papers-templates",{"id":50,"doc_module":9,"doc_module_name":10,"category_name":51,"show_sort_weight":4,"slug":52},158,"General","general-158",{"code":4,"msg":54,"data":55},"ok",{"site_id":56,"language":57,"slug":58,"title":59,"keywords":60,"description":61,"schema_data":62,"social_meta":120,"head_meta":122,"extra_data":124,"updated_unix":126},105,"en","template-protocol-ocr-903-instructions-and-protocol-sections","Template Protocol (OCR-903) - Instructions and Protocol Sections","","A protocol template titled “TEMPLATE PROTOCOL (OCR-903)” provides structured instructions for preparing a study protocol document using required sections and consistent formatting. It guides authors to mark non-applicable sections as “NA,” keep an electronic copy for updates, and remove italicized instructions before finalizing. The template includes fields for the principal investigator, version number/date, revision history, and a detailed table of contents covering study summary, objectives, background, endpoints, intervention, procedures, data management, privacy, consent processes, monitoring provisions, and research timelines.",{"@graph":63,"@context":119},[64,80,102],{"@type":65,"itemListElement":66},"BreadcrumbList",[67,71,74,77],{"item":68,"name":69,"@type":70,"position":9},"https://docshare.wps.com","Home","ListItem",{"item":72,"name":10,"@type":70,"position":73},"https://docshare.wps.com/template/",2,{"item":75,"name":36,"@type":70,"position":76},"https://docshare.wps.com/template/forms/",3,{"item":78,"name":59,"@type":70,"position":79},"https://docshare.wps.com/template/template-protocol-ocr-903-instructions-and-protocol-sections/244746/",4,{"url":78,"name":59,"@type":81,"image":82,"author":87,"headline":59,"publisher":90,"fileFormat":93,"inLanguage":57,"description":61,"dateModified":94,"datePublished":95,"encodingFormat":93,"isAccessibleForFree":96,"interactionStatistic":97},"DigitalDocument",{"url":83,"@type":84,"width":85,"height":86},"https://docshare.wps.com/thumbnails/template-protocol-ocr-903-instructions-and-protocol-sections/244746.png","ImageObject",442,249,{"name":88,"@type":89},"Noah","Person",{"url":68,"name":91,"@type":92},"DocShare","Organization","application/pdf","2026-10-23","2026-09-12",true,{"@type":98,"interactionType":99,"userInteractionCount":101},"InteractionCounter",{"@type":100},"ViewAction",9,{"@type":103,"mainEntity":104},"FAQPage",[105,111,115],{"name":106,"@type":107,"acceptedAnswer":108},"What should be done with sections that do not apply to the study?","Question",{"text":109,"@type":110},"Mark those sections as “NA.” For subsections, such as 1.x or 8.x, delete the subsection if it is not applicable.","Answer",{"name":112,"@type":107,"acceptedAnswer":113},"Which items must be removed before finalizing the protocol?",{"text":114,"@type":110},"Remove all instructions in italics so they are not included in the final protocol document.",{"name":116,"@type":107,"acceptedAnswer":117},"What information must be included in the principal investigator section?",{"text":118,"@type":110},"Include the principal investigator’s name, department, telephone number, and email address.","https://schema.org",{"og:url":78,"og:type":121,"og:title":59,"og:site_name":91,"og:description":61},"article",{"robots":123,"canonical":78},"index,follow",{"doc_id":125,"site_id":56},244746,1789221479,{"code":4,"msg":5,"data":128},{"doc_id":125,"user_id":129,"nickname":88,"user_avatar":130,"doc_module":9,"category_id":35,"category_name":36,"doc_title":59,"doc_description":61,"doc_content":131,"file_id":132,"file_url":133,"file_type":134,"file_size":135,"view_count":101,"is_deleted":4,"is_public":9,"is_downloadable":9,"audit_status":9,"page_count":20,"language":136,"language_code":57,"site_id":56,"html_lang":57,"table_of_contents":137,"faqs":138,"seo_title":139,"seo_description":61,"update_tm":126,"read_time":47},8796095462418,"https://ap-avatar.wpscdn.com/avatar/80000253c1241d02b47?x-image-process=image/resize,m_fixed,w_180,h_180&k=1778826106357471780","INSTRUCTIONS:  \n• Use “TEMPLATE PROTOCOL (OCR-903)” to prepare a document with the information from following sections.  \n• Depending on the nature of your study, some sections may not be applicable to your research. Ifso mark as “NA”. For example, research involving a retrospective chart review may have many sections with “NA.” For subsections, like 1.x or 8.x, you can delete it ifit’s not applicable.  \n• When you write a protocol, keep an electronic copy. You will need to modify this copy when making changes.  \n• As you are writing the protocol, remove all instructions in italics so that they are not contained in the final version of your protocol.  \n• Omit starred (*) items if this is the activation of a protocol at anew site or sites that will be overseen by a principal investigator who will take separate and full responsibility for that site or those sites. Complete by describing information specific to the site(s). Do not repeat information in the approved protocol that applies to all site(s).  \nPROTOCOL TITLE:  \nInclude the full protocol title.  \nPRINCIPAL INVESTIGATOR:  \nName  \nDepartment  \nTelephone Number  \nEmail Address  \nVERSION NUMBER/DATE:  \nInclude the version number and date of this protocol.  \nREVISION HISTORY  \n\n| Revision \\# | Version Date | Summary of Changes | Consent\u003Cbr>Change? |\n| --- | --- | --- | --- |\n|  |  |  |  |\n|  |  |  |  |\n|  |  |  |  |\n|  |  |  |  |\n|  |  |  |  |\n\nTable of Contents  \n1.0 Study Summary........................................................................................................ 3  \n2.0 Objectives* .............................................................................................................. 4  \n3.0 Background* ............................................................................................................ 4  \n4.0 Study Endpoints* ..................................................................................................... 4  \n5.0 Study Intervention/Investigational Agent ................................................................ 4  \n6.0 Procedures Involved* ............................................................................................... 5  \n7.0 Data and Specimen Banking* .................................................................................. 5  \n8.0 Sharing of Results with Subjects* ........................................................................... 6  \n9.0 Study Timelines* ..................................................................................................... 6  \n10.0 Inclusion and Exclusion Criteria* ............................................................................ 6  \n11.0 Vulnerable Populations* .......................................................................................... 6  \n12.0 Local Number of Subjects ....................................................................................... 7  \n13.0 Recruitment Methods ............................................................................................... 7  \n14.0 Withdrawal of Subjects* .......................................................................................... 7  \n15.0 Risks to Subjects* .................................................................................................... 7  \n16.0 Potential Benefits to Subjects* ................................................................................ 8  \n17.0 Data Management* and Confidentiality .................................................................. 8  \n18.0 Provisions to Monitor the Data to Ensure the Safety of Subjects* .......................... 8  \n19.0 Provisions to Protect the Privacy Interests of Subjects............................................ 9  \n20.0 Compensation for Research-Related Injury............................................................. 9  \n21.0 Economic Burden to Subjects .................................................................................. 9  \n22.0 Consent Process ....","cbCaidVHmLJJurGG","https://ap.wps.com/l/cbCaidVHmLJJurGG","pdf",216326,"English","# PROTOCOL TITLE\n# PRINCIPAL INVESTIGATOR\n# REVISION HISTORY\n# 1.0 Study Summary\n# 2.0 Objectives\n# 3.0 Background\n# 4.0 Study Endpoints\n# 5.0 Study Intervention/Investigational Agent\n# 6.0 Procedures Involved\n# 7.0 Data and Specimen Banking\n# 8.0 Sharing of Results with Subjects\n# 9.0 Study Timelines\n# 10.0 Inclusion and Exclusion Criteria\n# 11.0 Vulnerable Populations\n# 12.0 Local Number of Subjects\n# 13.0 Recruitment Methods\n# 14.0 Withdrawal of Subjects\n# 15.0 Risks to Subjects\n# 16.0 Potential Benefits to Subjects\n# 17.0 Data Management and Confidentiality\n# 18.0 Provisions to Monitor the Data to Ensure the Safety of Subjects\n# 19.0 Provisions to Protect the Privacy Interests of Subjects\n# 20.0 Compensation for Research-Related Injury\n# 21.0 Economic Burden to Subjects\n# 22.0 Consent Process\n# 23.0 Process to Document Consent in Writing\n# 24.0 Setting\n# 25.0 Resources Available\n# 26.0 Multi-Site Research","[{\"question\":\"What should be done with sections that do not apply to the study?\",\"answer\":\"Mark those sections as “NA.” For subsections, such as 1.x or 8.x, delete the subsection if it is not applicable.\"},{\"question\":\"Which items must be removed before finalizing the protocol?\",\"answer\":\"Remove all instructions in italics so they are not included in the final protocol document.\"},{\"question\":\"What information must be included in the principal investigator section?\",\"answer\":\"Include the principal investigator’s name, department, telephone number, and email address.\"}]","Template Protocol (OCR-903) - Instructions and Protocol Sections | PDF"]