[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"doc-detail-165550-en":3,"doc-seo-165550-105":30,"detail-sidebar-cat-1-en-105":90},{"code":4,"msg":5,"data":6},0,"success",{"doc_id":7,"user_id":8,"nickname":9,"user_avatar":10,"doc_module":11,"category_id":12,"category_name":13,"doc_title":14,"doc_description":15,"doc_content":16,"file_id":17,"file_url":18,"file_type":19,"file_size":20,"view_count":11,"is_deleted":4,"is_public":11,"is_downloadable":11,"audit_status":11,"page_count":21,"language":22,"language_code":23,"site_id":24,"html_lang":23,"table_of_contents":25,"faqs":26,"seo_title":27,"seo_description":15,"update_tm":28,"read_time":29},165550,1099513958762,"Logic","https://ap-avatar.wpscdn.com/avatar/1000023916a998db790?x-image-process=image/resize,m_fixed,w_180,h_180&k=1784791008015729253",1,17,"Forms","SBSREC Parental Informed Consent Form - Template","Parental Informed Consent Form template for enrolling a child in a research study under SBSREC oversight. It provides structured sections to record study details, sponsors, investigators, study rationale, procedures, duration, sample collection handling, and voluntary participation rights. The form outlines foreseeable risks and discomforts, potential benefits, confidentiality and data access, costs, reimbursement and compensation, alternatives to participation, and clear guidance on contact points for questions and participant rights.","PARTICIPANT ID: …………………………………\nPARENTAL INFORMED CONSENT FORM\nStudy Title:\nGive a clear and concise title of the research.\nSponsor(s) of the study:\nList the names of the sponsors and collaborating partners if any.\nList of investigators:\nIntroduction\nProvide a concise background of the study and a brief explanation of the study rationale – why the study is important.\nExplain the reason why the child is being asked to participate in the study, state the approximate number of children participating in the study and where it will be conducted.\nPurpose of the study:\nProvide a brief description of the purpose or what the study aims to achieve. Include a statement that this is a study rather than provision of clinical care \u003C\u003Cif applicable>>.\nProcedures:\nBriefly describe the procedures explaining how the child will be involved and what will be required of the child. Include a description of the experimental components of the study if any, such as testing a new intervention, new procedure etc.\nState the estimated duration the child will be involved in the study.\nIf a study involves sample collection, briefly state the sample type to be provided by the child, quantity and how it will be managed at the end. Inform the parent/ guardian that they will be asked to sign a separate consent form on behalf of the child if they agree to allow any left-over samples to be stored for future use. A separate consent form will also be needed for genetic testing which will be performed on the child’s sample \u003C\u003Cif applicable>>. Inform the parent/ guardian that the child can still participate in this study if they refuse genetic testing on the child’s samples or if they refuse to allow the researchers to store the child’s samples for a long time.\nProvide appropriate guidance on how the child will return to the standard of care after completion of their study visits \u003C\u003Cif applicable>>\n\u000f\nVoluntary Participation:\nState that participation is voluntary. State that the parent/ guardian has a right to refuse the child from participating in the study. If they choose to allow the child to participate in the study, he/she has the right to withdraw the child from the study at any time or withdraw from the study at any time without giving a reason and without any penalty or loss of benefits to which they or the child are otherwise entitled. Any research results obtained prior to your withdrawal of consent may however be used and some data may have                        already been published. Give circumstances under which the child may be removed from the study without the parent’s or guardian’s consent.\nAlternatives to Participation\nInform the parent/ guardian about what possible alternatives are available other than the child participating in the study e.g. alternative procedures or courses of treatment.\nRisks and Discomforts:\nDescribe the foreseeable risks and discomforts the child may experience while in this study (physical, social, economic and psychological). Also explain how risks will be minimized.\nInclude a statement that in case the child feels unwell, the parent/ guardian should feel free to contact the study team on [insert contact] and that if the child is referred to hospital for a research related injury/ illness, the cost of referral and management of the condition                     shall be paid by the study \u003C\u003Cif applicable>>.\nBenefits:\nDescribe the anticipated benefits to the child, benefits to research communities or to other children that may be reasonably expected to result from the study. On the contrary, if no direct benefits are expected to the children, include a statement clearly stating so.\nConfidentiality:\nDescribe how the privacy and confidentiality of the child’s information will be maintained during and after the study. Include how the child’s data will be stored and for how long.\nDescribe who will have access to data of the children. Include a statement that relevant research oversight bodies e.g. the School of Biomedical Sciences R","cbCaipEaKwipCUlN","https://ap.wps.com/l/cbCaipEaKwipCUlN","docx",47885,4,"English","en",105,"# Participant Information\n## Study Details\n## Sponsor(s) and Investigators\n# Study Description\n## Introduction and Purpose\n## Procedures and Duration\n## Voluntary Participation and Withdrawal\n## Alternatives to Participation\n# Ethical and Administrative Terms\n## Risks and Discomforts\n## Benefits\n## Confidentiality\n## Costs\n## Compensation and Reimbursement\n## Questions and Participant Rights\n## Ethical Approval\n## Dissemination of Findings","[{\"question\":\"What information must be completed at the start of the parental consent form?\",\"answer\":\"The form includes participant ID, the study title, sponsor(s) of the study, and a list of investigators, along with key study background and rationale.\"},{\"question\":\"What does the form require regarding procedures, sample collection, and study duration?\",\"answer\":\"It asks for a description of how the child will be involved, expected duration, and—if applicable—sample type, quantity, management at study end, and consent options for storage and genetic testing.\"},{\"question\":\"How does the form explain confidentiality, data access, and participant rights?\",\"answer\":\"It describes how the child’s information will be protected and stored, who can access the data, and that oversight bodies such as SBSREC and UNCST may access private information to ensure ethical and regulatory compliance. It also states the parent/guardian’s right to refuse or withdraw without penalty.\"}]","SBSREC Parental Informed Consent Form - Template | DOCX",1788173443,2,{"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":85,"head_meta":87,"extra_data":89,"updated_unix":28},"sbsrec-parental-informed-consent-form-template","",{"@graph":36,"@context":84},[37,52,67],{"@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/sbsrec-parental-informed-consent-form-template/165550/",{"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","2026-09-02","2026-08-31",true,{"@type":64,"interactionType":65,"userInteractionCount":21},"InteractionCounter",{"@type":66},"ViewAction",{"@type":68,"mainEntity":69},"FAQPage",[70,76,80],{"name":71,"@type":72,"acceptedAnswer":73},"What information must be completed at the start of the parental consent form?","Question",{"text":74,"@type":75},"The form includes participant ID, the study title, sponsor(s) of the study, and a list of investigators, along with key study background and rationale.","Answer",{"name":77,"@type":72,"acceptedAnswer":78},"What does the form require regarding procedures, sample collection, and study duration?",{"text":79,"@type":75},"It asks for a description of how the child will be involved, expected duration, and—if applicable—sample type, quantity, management at study end, and consent options for storage and genetic testing.",{"name":81,"@type":72,"acceptedAnswer":82},"How does the form explain confidentiality, data access, and participant rights?",{"text":83,"@type":75},"It describes how the child’s information will be protected and stored, who can access the data, and that oversight bodies such as SBSREC and UNCST may access private information to ensure ethical and regulatory compliance. 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