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The guide covers study identification details, investigator and funding information, participant-facing purpose and eligibility rationale, and clear descriptions of what participants will do and the expected duration. 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For sheets of 3 pages or less, delete the Key Information heading and its instructions.",{"name":115,"@type":106,"acceptedAnswer":116},"How should risks and confidentiality protections be described?",{"text":117,"@type":109},"Risks must be disclosed and may include physical, emotional, social, or legal risks. 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The purpose of this form is to provide you information that may affect your decision as to whether or not to participate. Your participation is entirely voluntary, and you can refuse to participate at any time without penalty.\nKey Information: [If information sheet is less than 3 pages long delete this section]\n[If the information sheet will be longer than 3 pages – you must use this key information section to provide a concise summary with enough detail that a reasonable person can clearly see what participant will be asked to do, risks and benefits and why subject may or may not want to participate. See \u0013HYPERLINK \"https://research.wayne.edu/irb/docs/key_information_guidance_2_7_19.pdf\"\u0014Key Information guidance\u0015 for more information. If this form is 3 pages or less, delete this heading and instructions]\nWhat is this study about & why is it being done?\nYou are being asked to participate in a research study about [insert a general statement about the study and why it is being conducted] because you [explain why the prospective participant is eligible to participate]. This study is being conducted at Wayne State University [and: state all other locations where the study will be conducted].. The purpose of this form is to provide you information to decide whether or not to you want to participate in this research study. Your participation is entirely voluntary, and you can refuse to participate or withdraw at any time without penalty.\nWhat Will I Do and How Long Will It Take? [Explain in simple, non-scientific terms what the participant will be asked to do as part of the research study. Be concise; avoid describing study procedures in lengthy narrative form.\nIf you take part in the study, you will be asked to [List all tasks participant’s will be asked to do (e.g., fill out surveys, complete questionnaires, participate in focus groups etc) in chronological order including the expected duration for each activity. Explain the nature of the questions that will be asked] If the study will involve audio/video recording please use template language in the Information Sheet Appendix.]\nWhat are the Possible Benefits of participating in this study? [list possible benefits described below applicable to the study]\nIf there are direct benefits to participants: [List direct benefit to the participant (if any). Direct benefit is a tangible outcome to individual participants that is a direct result of the research. Do not include compensation here; you’ll describe that below.] In addition to these direct benefits, your participation in this study may generate information that could benefit other people now or in the future.\nIf there are no direct benefits to participants: This study is not designed with a direct benefit to participants, however, [Select only the applicable statement(s) that follows]\nStatement 1: You may receive some indirect benefit [list indirect benefit to the participant, i.e., reflecting on experience or better understanding of oneself or topic]\nStatement 2: Information from this study may benefit other people now or in the future.\nWhat are the risks and discomforts of participating in this study?\n[Informed consent must disclose all risks that apply to the study. Risks can be physical, emotional, social, or legal in nature. Sample language for some risks is provided below. You may use and/or edit the sample language provided below. Include measures you will take to minimize risks]\nThe risks to participating in this study are similar to risks encountered in everyday life. These ris","cbCaipbE57q4xPGp","https://ap.wps.com/l/cbCaipbE57q4xPGp","doc",108544,7,"English","# TEMPLATE GUIDE:\n## Research Information Sheet\n## Title of Study\n## Principal Investigator (PI) and Funding Source\n## Introduction and Voluntary Participation\n## Key Information (When Applicable)\n## Study Purpose and Eligibility\n## What Will I Do and How Long Will It Take\n## Possible Benefits\n## Risks and Discomforts\n## Cost and Compensation\n## Participation Alternatives","[{\"question\":\"What sections must be completed in the RIS template?\",\"answer\":\"The RIS includes fields for the study title, principal investigator (PI) details, department and phone, funding source (deleted if none), an introduction, and sections describing key information, study purpose, tasks and timing, benefits, risks, costs, and compensation.\"},{\"question\":\"When should the “Key Information” section be included?\",\"answer\":\"Include the Key Information section only when the information sheet is longer than 3 pages. For sheets of 3 pages or less, delete the Key Information heading and its instructions.\"},{\"question\":\"How should risks and confidentiality protections be described?\",\"answer\":\"Risks must be disclosed and may include physical, emotional, social, or legal risks. Confidentiality risk should be addressed with specific measures such as anonymizing data or removing identifiers, defining retention timing, encrypting password-protected electronic storage, and controlling how identifiers link to research data.\"}]","Research Information Sheet (RIS) Template Guide - Instructions | DOC",1788197597]