[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"doc-detail-165319-en":3,"doc-seo-165319-105":30,"detail-sidebar-cat-1-en-105":91},{"code":4,"msg":5,"data":6},0,"success",{"doc_id":7,"user_id":8,"nickname":9,"user_avatar":10,"doc_module":11,"category_id":12,"category_name":13,"doc_title":14,"doc_description":15,"doc_content":16,"file_id":17,"file_url":18,"file_type":19,"file_size":20,"view_count":4,"is_deleted":4,"is_public":11,"is_downloadable":11,"audit_status":11,"page_count":21,"language":22,"language_code":23,"site_id":24,"html_lang":23,"table_of_contents":25,"faqs":26,"seo_title":27,"seo_description":15,"update_tm":28,"read_time":29},165319,549768064778,"Felix Montgomery","https://ap-avatar.wpscdn.com/davatar_6f874abed73319feea01a86fa6f0fab8",1,17,"Forms","Social & Behavioral Template - Instructions","Social & Behavioral Template with instructions for preparing a protocol for social and behavioral research submitted to an IRB. The template guides completion of required sections such as protocol title, version date, principal investigator details, study personnel, and study type (dissertation, thesis, capstone). It structures key scientific content including purpose and aims, background and literature rationale, inclusion and exclusion criteria, data collection procedures, and the schedule of activities, overall design, timelines, safety monitoring, and data sources. Instructions in red must be removed prior to submission.","SOCIAL & BEHAVIORAL TEMPLATE WITH INSTRUCTIONS:\nUse this template to prepare a document for social and behavioral research with the information from the following sections.\nIf your study will ONLY involve secondary use of data and/or specimens. See HRP-503b TEMPLATE SECONDARY USE PROTOCOL.\nDepending on the nature of what you are doing, some sections may not be applicable to your research. Mark N/A if it’s not applicable.\nWhen you write a protocol, keep an electronic copy. You will need to modify this copy when making changes.\nRemove all instructions in red before submitting to the IRB or use the version without instructions and use this copy as a guide.\nPROTOCOL TITLE:\nInclude the full protocol title.\nProtocol VERSION DATE:\nPRINCIPAL INVESTIGATOR:\n(Under graduate and Graduate Students are not allowed to be Principal Investigators. List student researcher below.)\nName\nDepartment\nTelephone Number\nEmail Address\nSTUDY PERSONNEL:\nIs this study is part of a dissertation or thesis:\n\u0003☐\u0004  Yes              \u0003☐\u0004  No\nIs this study is part of a capstone project:\n\u0003☐\u0004  Yes              \u0003☐\u0004  No\nCheck any applicable boxes in the table below – you will be asked for further detail on these topics later in the protocol form:\n1.0  Purpose of the Study:\nDescribe the purpose, specific aims, or objectives. State the hypotheses to be tested or the research questions that will guide the study.\n2.0  Background / Literature Review / Rationale for the study:\nBriefly (500 words or fewer):\nDescribe the relevant current context of the study and gaps in current knowledge.\nProvide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge.\nAdd relevant references at the end of the protocol (not at the end of this section).\nIf you are uploading a funding proposal that has this information, indicate applicable pages.\n3.0  Inclusion and exclusion criteria:\nBriefly describe the total number of participants and the criteria (such as age, gender, language, etc.) that define who will be included or excluded in your study sample.\nIndicate specifically whether you will include or exclude any special populations: (You may not include members of these populations as participants in your research unless you indicate this in your inclusion criteria.)\nAdults unable to consent\nMinors: infants, children, teenagers\nPregnant women (where the activities of the research may affect the pregnancy or the fetus.)\nPrisoners\n4.0A  Procedures Involved:\nPlease check the boxes for all applicable data collection procedures you plan to use:\n\u0003☐\u0004One-on-one interviews\n\u0003☐\u0004Focus Groups\n\u0003☐\u0004Questionnaires/surveys\n\u0003☐\u0004Secondary Data Analysis (medical record data, educational records, government or private sector datasets, etc.)\n\u0003☐\u0004Ethnographic observation\n\u0003☐\u0004 Diagnostic or Mental Health Assessment Tools\n\u0003☐\u0004Physiological measurements (e.g., EEG, EKG, MRI)\n\u0003☐\u0004Biospecimen collection (saliva samples, blood draws, hair samples, etc.)\n\u0003☐\u0004Mobile applications/data collection devices (e.g., Fitbits, actigraphs, etc.)\n\u0003☐\u0004Behavioral decision making tasks (e.g., puzzles, interactive games, etc.)\n\u0003☐\u0004Physical activities such as walking and other forms of exercise\n\u0003☐\u0004Other procedures (briefly list types of procedures here if not covered by the check-boxes above): ______________________________________________\n4.0B  Schedule of Activities:\nThe schedule of activities (SOA) must capture the procedures that will be accomplished at each study visit, and all contact with study participants (e.g., telephone contacts). This includes any screening procedures that are used for eligibility, participant randomization or stratification, or decisions on study intervention discontinuation. Include procedures that contribute to participant eligibility, study objectives and endpoints.\nThe schedule below is provided as an example and should be modified as appropriate.\n4.0C  Overall Design:\nDescribe the setting of the study, in","cbCaimwKhd0IcBTm","https://ap.wps.com/l/cbCaimwKhd0IcBTm","docx",69089,14,"English","en",105,"# Protocol Information\n## Purpose of the Study\n## Background / Literature Review / Rationale\n## Inclusion and Exclusion Criteria\n## Procedures Involved\n## Schedule of Activities\n## Overall Design","[{\"question\":\"What is the main purpose of this Social \\u0026 Behavioral template?\",\"answer\":\"It provides a structured protocol format for social and behavioral research, using information from required sections to support IRB submission.\"},{\"question\":\"What should researchers do with the instructions included in the template before submitting to the IRB?\",\"answer\":\"Remove all instructions in red before submitting, or use the version without instructions and keep the current copy for later edits.\"},{\"question\":\"What types of participant inclusion and data collection details are required?\",\"answer\":\"The protocol must include inclusion/exclusion criteria and indicate applicable participant special populations, then specify the procedures used (e.g., interviews, focus groups, surveys, secondary data analysis, and other listed methods).\"}]","Social & Behavioral Template - 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