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Participation in research is completely voluntary.\nThe purpose of the study is to [one sentence explanation of why].\nThe study will take a total of [total time commitment] and you will be asked to [one sentence explanation of study procedures].\nRisks and/or discomforts may include [list possible risks and/or discomforts].\nThere is no direct benefit to you [or list possible direct benefits]. The results from the study may [one sentence explanation of societal benefits of study].\n[If applicable, list appropriate alternative procedures or courses of treatment].\n*Key information is required for consent forms over two pages in length, where a page is one side of a standard 8.5x11 inch document.\nKey Information - EXAMPLE\nYou are being invited to participate in a research study. Participation in research is completely voluntary.\nThe purpose of the study is to examine the effect of providing key information to subjects in a consent form on their comprehension of the study.\nThe study will take a total of one hour and you will be asked to read the consent form and answer questions about it.\nRisks and/or discomforts may include the risk of breach of confidentiality.\nThere is no direct benefit to you. The results from the study may show whether this additional consent element is helpful to subjects.\nIntroduction\nMy name is _______________, [M.D./Ph.D.,] [if there are co-investigators, note here, e.g., \"and my research colleagues are ___________, M.D. and ___________, Ph.D.\"]  I am a(n) [undergraduate/ graduate student/ faculty member] at the University of California, Berkeley, [if lead investigator is a student, introduce faculty sponsor here, e.g., \"working with my faculty advisor, Professor ___________,\"] in the School/Department of ___________.  I am [We are] planning to conduct a medical research study, which I invite you to take part in.\nYou are being invited to participate in this study because you are/have [specify prospective subject's medical condition or other reason for recruitment to study].\nPurpose\nThe purpose of this study is to __________.  [Give brief explanation of why study is being done, using one or two sentences written in clear language understandable to the target population].\n[Any investigational drug(s) or device(s) to be used in the study should be noted and named. The name by which the drug or device is referred to in this section should be used consistently throughout the form.]\n[If appropriate: About [state total accrual goal for number of subjects] people will take part in this study.  [Give a short description about cohorts, if any.  For multi-center studies, give figures both for the whole study and for local enrollment at UCB.]\nProcedures\nIf you agree to be in this study, you will be asked to do the following: [Discuss screening procedures first, if any, or refer to a separate screening consent form if used.  List and describe tests/ procedures and their frequency.  Clearly identify any procedures or elements of a procedure that are experimental.  Indicate location where procedures will take place (e.g., lab, hospital, home, or other setting), and amount of time needed for each procedure.  Also note total amount of time required for subject’s study participation, at the beginning or end of this section.]\n[If there are screening procedures:]\nBefore you begin the main part of the study...\nYou will need to have the following screening exams/ tests/ procedures to find out if you can be in the main part of the study. [List and describe tests/ procedures as appropriate.  If more than one screening procedure will be done, use bulleted format.]\nFor example:\nPhysical exam:  You will have a physical examination, similar to those done for regular medical care.\nMedical chart review:  Your medical ch","cbCait1laoV3uJjx","https://ap.wps.com/l/cbCait1laoV3uJjx","docx",107507,10,"English","# Consent to Participate in Research\n## Key Information\n## Introduction\n## Purpose\n## Procedures\n## Screening Procedures (if applicable)","[{\"question\":\"Is participation in the research study voluntary?\",\"answer\":\"Yes. Participation is completely voluntary.\"},{\"question\":\"What information sections are included for informed consent?\",\"answer\":\"The template includes key information (study purpose, time commitment, procedures, risks/discomforts, and benefits), an introduction of the investigator and affiliation, the study purpose, and detailed procedures including screening options if applicable.\"},{\"question\":\"How does the template handle potential risks and benefits?\",\"answer\":\"It prompts for a list of possible risks and/or discomforts and clarifies that there may be no direct benefit to the participant, while the results may provide broader societal benefits.\"}]","CF Template Biomedical - Consent Form - Participate in Research | DOCX",1788278336]