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Includes dedicated sections for describing risks and benefits, selecting confidentiality or anonymity language, outlining compensation terms, and stating participant rights to refuse, skip questions, or withdraw at any time. Provides guidance for researcher contact, focus group limits, legal reporting obligations, and future use or nonuse of research data, plus disclosure of relevant results when applicable.","Remove all blue content within brackets and anything that is not relevant – modify to fit your study\nSee the “general requirements for informed consent” document for details on what must be present in a consent form\nKey Information\nThis is a voluntary research study on [insert general statement about study].\nThis [duration] study involves [explain what the participants will do].\nThe benefits include [state any benefits to the participant/field of study]; the risks include [state any risks or the lack thereof].\nDescription of the Study\nThe purpose of the study is [explain research question and purpose in lay language]. If you agree to be in this study, you will be asked to do the following things: [explain procedures and tasks; describe length of time for participation, frequency and duration of procedures; etc. in a clear, concise manner]\n*[If applicable, explain any alternative procedures or courses of treatment available to the subject.]\nRisks and Benefits\nThe study has the following risks.  First, [explain first risk, including the likelihood of the risk]. Second, [explain second risk, including the likelihood of the risk].  Third, …\n*[If there are no foreseeable risks, state as such] There are no reasonably foreseeable (or expected) risks.\nThe benefits of participation are [explain benefits of participation that may reasonably be expected from the research to the participants and/or other. These can be direct benefits to the participants, and/or benefits to others from the knowledge gained from the research]\n*[If there are no expected benefits directly to the participants, state as such.]\nConfidentiality [or anonymity – you pick which term is appropriate based on identifiers]\n[include only the information below that is relevant for your study]\nThis study is anonymous.  We will not be collecting or retaining any information about your identity.\n[or]\nThe records of this study will be kept confidential to the fullest extent provided by law. Research records will be kept in a locked file, and all electronic information will be coded and secured using a password protected file. [If audio or video tape recordings are made, explain specifically who will have access to them, if they will be used for educational purposes, and when they will be erased/destroyed and indicate how they will be destroyed or erased.]  We will not include any information in any report we may publish that would make it possible to identify you.\n[and possibly]\nWith your permission, your identity will be made known in written materials resulting from the study.  However, you will be given the opportunity to review and approve any material that is published about you.\n[If participation involves a focus group, add the following statement:]\nIt should be understood that, when participating in a focus group, confidentiality among the members of the group cannot be guaranteed.\n[If there are legal reporting requirements for information that may be disclosed by participants during the research, such as for suspected child abuse, sexual assault, or elder abuse, this must be stated in the consent form.]\nCompensation\nYou will receive the following compensation for your time: [explain amount of payment or other reimbursement information (e.g., class points, tokens, donations, etc.), as well as when payment and/or reimbursement will occur and in what cases payment will not occur if any. If there will be no payment, eliminate this section.]\nYour Rights\nThe decision to participate in this study is entirely up to you.  You may refuse to take part in the study at any time.  Your decision will not result in any loss of benefits to which you are otherwise entitled.  You have the right to skip any question or research activity, as well as to withdraw completely from participation at any point during the process.\nYou have the right to ask questions about this research study and to have those questions answered before, during, or after the research.  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The template also includes the right to ask questions before, during, or after the study and to contact the researcher and an appropriate compliance office if concerns remain.\"}]","Key Information - Informed Consent Form Template | DOCX",1788239800,2,{"code":4,"msg":31,"data":32},"ok",{"site_id":24,"language":23,"slug":33,"title":14,"keywords":34,"description":15,"schema_data":35,"social_meta":86,"head_meta":88,"extra_data":90,"updated_unix":28},"key-information-informed-consent-form-template","",{"@graph":36,"@context":85},[37,52,68],{"@type":38,"itemListElement":39},"BreadcrumbList",[40,44,47,50],{"item":41,"name":42,"@type":43,"position":11},"https://docshare.wps.com","Home","ListItem",{"item":45,"name":46,"@type":43,"position":29},"https://docshare.wps.com/template/","Template",{"item":48,"name":13,"@type":43,"position":49},"https://docshare.wps.com/template/forms/",3,{"item":51,"name":14,"@type":43,"position":21},"https://docshare.wps.com/template/key-information-informed-consent-form-template/168943/",{"url":51,"name":14,"@type":53,"author":54,"headline":14,"publisher":56,"fileFormat":59,"inLanguage":23,"description":15,"dateModified":60,"datePublished":61,"encodingFormat":59,"isAccessibleForFree":62,"interactionStatistic":63},"DigitalDocument",{"name":9,"@type":55},"Person",{"url":41,"name":57,"@type":58},"DocShare","Organization","application/vnd.openxmlformats-officedocument.wordprocessingml.document","2026-09-04","2026-09-01",true,{"@type":64,"interactionType":65,"userInteractionCount":67},"InteractionCounter",{"@type":66},"ViewAction",6,{"@type":69,"mainEntity":70},"FAQPage",[71,77,81],{"name":72,"@type":73,"acceptedAnswer":74},"What key elements must be included in this informed consent form?","Question",{"text":75,"@type":76},"The template specifies a voluntary study statement, what participants will do and for how long, the study purpose, and the risks and benefits. It also requires confidentiality/anonymity language, compensation (if any), and participant rights.","Answer",{"name":78,"@type":73,"acceptedAnswer":79},"How does the template handle confidentiality or anonymity?",{"text":80,"@type":76},"It provides alternative language paths: one option states the study is anonymous and no identity information is collected or retained. Another option describes coded and password-secured records kept confidential to the fullest extent allowed by law, with no reportable information that could identify participants.",{"name":82,"@type":73,"acceptedAnswer":83},"What rights do participants have under this consent template?",{"text":84,"@type":76},"Participants can refuse to take part, skip any question or activity, and withdraw completely at any point without losing entitled benefits. 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