[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"doc-seo-176685-105":3,"detail-sidebar-cat-1-en-105":81,"doc-detail-176685-en":127},{"code":4,"msg":5,"data":6},0,"ok",{"site_id":7,"language":8,"slug":9,"title":10,"keywords":11,"description":12,"schema_data":13,"social_meta":74,"head_meta":76,"extra_data":78,"updated_unix":80},105,"en","point-form-consent-form-template","Point-form Consent Form Template","","Point-form consent form template designed for behavioural research studies, providing a structured overview of minimum required sections and layout guidance. The template details participant and researcher information, research purpose and objectives, procedures, funding, potential risks and risk mitigation, potential benefits, compensation, confidentiality and data storage, right to withdraw, follow-up information, and questions or concerns contact pathways. It also includes ethics approval acknowledgment and selectable consent options to support consistent alignment with an ethics application.",{"@graph":14,"@context":73},[15,34,56],{"@type":16,"itemListElement":17},"BreadcrumbList",[18,23,27,31],{"item":19,"name":20,"@type":21,"position":22},"https://docshare.wps.com","Home","ListItem",1,{"item":24,"name":25,"@type":21,"position":26},"https://docshare.wps.com/template/","Template",2,{"item":28,"name":29,"@type":21,"position":30},"https://docshare.wps.com/template/forms/","Forms",3,{"item":32,"name":10,"@type":21,"position":33},"https://docshare.wps.com/template/point-form-consent-form-template/176685/",4,{"url":32,"name":10,"@type":35,"image":36,"author":41,"headline":10,"publisher":44,"fileFormat":47,"inLanguage":8,"description":12,"dateModified":48,"datePublished":49,"encodingFormat":47,"isAccessibleForFree":50,"interactionStatistic":51},"DigitalDocument",{"url":37,"@type":38,"width":39,"height":40},"https://docshare.wps.com/thumbnails/point-form-consent-form-template/176685.png","ImageObject",442,249,{"name":42,"@type":43},"Maeve","Person",{"url":19,"name":45,"@type":46},"DocShare","Organization","application/vnd.openxmlformats-officedocument.wordprocessingml.document","2026-10-23","2026-09-02",true,{"@type":52,"interactionType":53,"userInteractionCount":55},"InteractionCounter",{"@type":54},"ViewAction",9,{"@type":57,"mainEntity":58},"FAQPage",[59,65,69],{"name":60,"@type":61,"acceptedAnswer":62},"What participant and researcher details are required in this consent form template?","Question",{"text":63,"@type":64},"The template requests project title; researcher(s) information including name, position, department, university, phone, and email; and supervisor details. It also includes optional fields for co-investigators and research assistants.","Answer",{"name":66,"@type":61,"acceptedAnswer":67},"How does the template describe procedures and the expected time commitment?",{"text":68,"@type":64},"It includes a section to describe exactly what participants must do and where, and to state the study duration in minutes.",{"name":70,"@type":61,"acceptedAnswer":71},"What confidentiality and data storage protections does the template include?",{"text":72,"@type":64},"It specifies that data will be kept confidential, linked to arbitrary participant numbers, summarized in aggregate form, and that consent forms won’t be linked to data. It also provides secure storage by the supervisor and typical destruction timelines, including minimum retention if published or presented.","https://schema.org",{"og:url":32,"og:type":75,"og:title":10,"og:site_name":45,"og:description":12},"article",{"robots":77,"canonical":32},"index,follow",{"doc_id":79,"site_id":7},176685,1790009496,{"code":4,"msg":82,"data":83},"success",[84,89,94,99,104,109,113,118,123],{"id":85,"doc_module":22,"doc_module_name":25,"category_name":86,"show_sort_weight":87,"slug":88},11,"Presentations",90,"presentations",{"id":90,"doc_module":22,"doc_module_name":25,"category_name":91,"show_sort_weight":92,"slug":93},12,"Resumes",80,"resumes",{"id":95,"doc_module":22,"doc_module_name":25,"category_name":96,"show_sort_weight":97,"slug":98},14,"Invoices",70,"invoices",{"id":100,"doc_module":22,"doc_module_name":25,"category_name":101,"show_sort_weight":102,"slug":103},15,"Posters",60,"posters",{"id":105,"doc_module":22,"doc_module_name":25,"category_name":106,"show_sort_weight":107,"slug":108},16,"Social Media",50,"social-media",{"id":110,"doc_module":22,"doc_module_name":25,"category_name":29,"show_sort_weight":111,"slug":112},17,40,"forms",{"id":114,"doc_module":22,"doc_module_name":25,"category_name":115,"show_sort_weight":116,"slug":117},18,"Letters",30,"letters",{"id":119,"doc_module":22,"doc_module_name":25,"category_name":120,"show_sort_weight":121,"slug":122},21,"Paper Templates",5,"papers-templates",{"id":124,"doc_module":22,"doc_module_name":25,"category_name":125,"show_sort_weight":4,"slug":126},158,"General","general-158",{"code":4,"msg":82,"data":128},{"doc_id":79,"user_id":129,"nickname":42,"user_avatar":130,"doc_module":22,"category_id":110,"category_name":29,"doc_title":10,"doc_description":12,"doc_content":131,"file_id":132,"file_url":133,"file_type":134,"file_size":135,"view_count":55,"is_deleted":4,"is_public":22,"is_downloadable":22,"audit_status":22,"page_count":30,"language":136,"language_code":8,"site_id":7,"html_lang":8,"table_of_contents":137,"faqs":138,"seo_title":139,"seo_description":12,"update_tm":140,"read_time":22},5909877438554,"https://ap-avatar.wpscdn.com/avatar/5600025385ad2bf12a7?_k=1778553567797529272","Instructions: This template is intended to provide an overview of the basic content required and a sample lay-out for a point form version of a consent form. Please adapt the content and language of the form for your study and ensure that it is appropriate for your participants (e.g., children). This template outlines the minimum information that must be included; please consult the consent form guidelines for additional information.  Also, please ensure that there is consistency between the content of your ethics application and your Consent Form.\nPoint-form Consent Form Template\nProject Title:\nResearcher(s): [YOUR NAME, POSITION (Faculty, Graduate or Undergraduate Student, Post Doc, Staff), DEPARTMENT, UNIVERSITY, PHONE, EMAIL]\nSupervisor: [SUPERVISOR’S NAME, DEPARTMENT, PHONE NUMBER, EMAIL]\n[IF APPLICABLE]: List co-Investigator(s), Research Assistants individually: NAME(S), DEPARTMENT, INSTITUTION, PHONE, EMAIL.\nPurpose(s) and Objective(s) of the Research:\nThe primary purpose of the research is to train the student researcher in the methods of behavioural research.  [Then state the specific purpose of your study.]\nProcedures: (See consent guidelines section 4)\n[Describe exactly what the participant is required to do and where?]  The study should take approximately [specify time] minutes of your time.\nPlease feel free to ask any questions regarding the procedures and goals of the study or your role.\nFunded by: [IF APPLICABLE] (see consent guidelines section 5)\nPotential Risks: (see guidelines section 6)\nThere are no known or anticipated risks to you by participating in this research or [E.G., EMOTIONAL, SOCIAL, PSYCHOLOGICAL, PHYSICAL, ECONOMIC, ETC.]\nRisk(s) will be addressed by [EXPLAIN; include referrals for counseling and other services; e.g.,  If any part of your participation in this study has made you feel uncomfortable, distressed, or upset, we encourage you to contact the University’s Student Counseling Centre (306) 966-4920), located in the 3rd floor of Place Riel Student Centre.]\nAt the end of the study you will be given a sheet that better explains the nature of the study and you will be given a chance to ask any further questions that you might have.\nPotential Benefits: [IF APPLICABLE] (see consent guidelines section 7)\nYou may receive no personal benefits from participation in the study.\nCompensation: [IF APPLICABLE] (see guidelines section 8)\n[Describe compensation]\nConfidentiality: (see consent guidelines section 9)\nYour data will be kept completely confidential and no personally identifying information will be linked to your data. Data will be coded using arbitrary participant numbers that will not be associated with any names or personally identifying information. Consent forms will not be linked with the data. All data will be summarized in aggregate form.  [Describe procedures to safeguard confidentiality and anonymity of responses; or explain limits to anonymity or justify why anonymity is not required].\nPlease indicate that if participants contact the researchers by email or by other means that provides identifying information then anonymity is lost but confidentiality of the participant will remain protected.\nStorage of Data: [If data will be anonymous, this section may be omitted]\nThe data and consent forms will be stored securely at the University of Saskatchewan by the supervisor.  Normally, the data will be destroyed once the course has been completed.  In instances where the data is published in an academic journal and/or presented at a professional conference, the data will be stored for a minimum of five years after completion of the study.  When the data is no longer required, it will be destroyed beyond recovery.\nRight to Withdraw:  (see consent guidelines section 10)\nYour participation is voluntary and you can answer only those questions that you are comfortable with.  You may withdraw from the research project for any reason, at any time without explanation or penalty of any sort. [if using ","cbCaiefqjM79hCTT","https://ap.wps.com/l/cbCaiefqjM79hCTT","docx",27373,"English","# Point-form Consent Form Template\n## Project information and participants\n## Purpose, procedures, and funding\n## Risks, benefits, and compensation\n## Confidentiality, data storage, and withdrawal\n## Follow-up, questions, approval, and consent options","[{\"question\":\"What participant and researcher details are required in this consent form template?\",\"answer\":\"The template requests project title; researcher(s) information including name, position, department, university, phone, and email; and supervisor details. It also includes optional fields for co-investigators and research assistants.\"},{\"question\":\"How does the template describe procedures and the expected time commitment?\",\"answer\":\"It includes a section to describe exactly what participants must do and where, and to state the study duration in minutes.\"},{\"question\":\"What confidentiality and data storage protections does the template include?\",\"answer\":\"It specifies that data will be kept confidential, linked to arbitrary participant numbers, summarized in aggregate form, and that consent forms won’t be linked to data. It also provides secure storage by the supervisor and typical destruction timelines, including minimum retention if published or presented.\"}]","Point-form Consent Form Template | DOCX",1788325239]