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Remember to erase these instructions and brackets when preparing your consent forms.  Make sure that your consent form has been proofread for typographical, grammar, and spelling errors.  Refer to the consent form samples in the \u0013 HYPERLINK \"https://www.sjsu.edu/research/docs/irb-consent-handbook.pdf\" \u0014Informed Consent Handbook\u0015 Appendix A for examples of wording.]\nREQUEST FOR YOUR PARTICIPATION IN RESEARCH\nTITLE OF THE STUDY\nNAME OF THE RESEARCHERS  [In addition to your name, also include your title or affiliation in this section, for example, Ph.D. or San Jose State University graduate student.  If you are a student, include your faculty supervisor’s name also. For example:\u000b\u000bLisa Simpson, San Jose State University graduate student, Psychology Department\u000bDr. Montgomery Burns, San Jose State University faculty supervisor, Psychology Department]\nYou may include an introductory statement about yourself and your research preceding the consent information. The introductory statement is optional.]\nPURPOSE\u000b[Describe what your study is about and why the study is being conducted.]\nPROCEDURES\u000b[Describe what participants will be asked to do, where and when the study will occur, the duration, and what materials and devices will be used – including the use of audio/video recording devices.]\u000b\u000bPOTENTIAL RISKS\u000b[Describe any foreseeable risk or discomforts to the participants. Include information on how risks will be mitigated as well as any appropriate supportive services that are available, when applicable. For research involving more than minimal risk, provide an explanation as to whether any treatments are available if injury occurs and, if so, what they consist of, or where further information may be obtained.]\nPOTENTIAL BENEFITS\u000b[Describe any possible direct benefits to participants, such as health, educational, or social benefits. If there are no direct benefits, please state this.]\nINCENTIVES AND COMPENSATION\u000b[Provide information about the amount, nature, and reason for any  incentives or compensation being offered for participation.  Otherwise, state that there is no incentive or compensation for participation.]\nCONFIDENTIALITY\u000b[Describe the manner and degree to which confidentiality will be maintained and who has access to identifying information.  Explain if there are any limits to confidentiality – for example, if you are a mandated reporter.  Avoid using the word “anonymous” unless you are certain that the research team will not be receiving any identifying information from participants.  If identifying information will be included in publication or dissemination, the degree to which participants will be identified and how they will be identified should be stated.]\nPARTICIPANT RIGHTS\u000b[The following sample text summarizes participants’ rights.]\nYour participation in this study is completely voluntary.  You can refuse to participate in the entire study or any part of the study without any negative effect on your relations with San Jose State University or [name any other participating institutions].  You also have the right to skip any question you do not wish to answer.  This consent form is not a contract.  It is a written explanation of what will happen during the study if you decide to participate.  You will not waive any rights if you choose not to participate, and there is no penalty for stopping your participation in the study.\nQUESTIONS OR PROBLEMS\u000b[The following sample text summarizes the contacts that need to be included on the consent form. ]\nYou are encouraged to ask questions at any time during this study.\nFor further information about the study, please contact [name of researcher and contact information – phone or email or both].\nComplaints about the research may be presented to [name and contact information for your department chair or college dean if there is no chair; make sure to include their title].\nFor questions about participants’ rights ","cbCaii9rMFJV5I3d","https://ap.wps.com/l/cbCaii9rMFJV5I3d","docx",16310,"English","# 参与研究申请\n## 研究标题与研究者信息\n## 研究目的\n## 研究程序\n## 潜在风险\n## 潜在收益\n## 激励与补偿\n## 保密\n## 参与者权利\n## 问题或投诉联系\n## 签署与研究者声明","[{\"question\":\"知情同意书中需要包含哪些关键信息？\",\"answer\":\"需要包含研究标题、研究者姓名与单位信息、研究目的、研究程序、潜在风险与风险缓解、潜在收益，以及激励与补偿（如有）。\"},{\"question\":\"如何说明潜在风险与风险缓解？\",\"answer\":\"应描述可预见的风险或不适，并说明如何减轻风险；若风险超过最低风险要求，还需解释是否有任何受伤治疗及其内容或进一步信息获取途径。\"},{\"question\":\"参与者的权利和咨询联系人如何写？\",\"answer\":\"需要明确参与完全自愿、可随时拒绝或跳过问题且不产生负面影响，并说明同意书不是合同。还需提供研究相关问题的联系人，以及关于参与者权利或伤害申诉的联系信息。\"}]","IRB研究知情同意书模板 - 参与研究申请 | DOCX",1788325238]