Parental Informed Consent Form Template-Q & A Format (UPDATED: 1.24.22) Informed Consent Form Template-Standard Format (UPDATED: 1.24.22) Informed Consent Form Template-Q & A Format (UPDATED: 1.24.22) Researchers are strongly advised to copy/print the stamped consent form for use during the study-doing so assures the current IRB-approved version is used and assures participants that the study has been reviewed by the IRB. Avoid including unnecessary headings (e.g., Attachment or Appendix) on the consent form. Please leave a 1 ½ inch margin at the top of the document to accommodate the stamp. Detailed guidance and a checklist are available to aid researchers.Īn IRB-approval stamp will be applied to approved consent forms. However, all of the consent elements must be included in your consent form unless your study is eligible for exempt review.Ĭonsent forms must be carefully drafted to facilitate comprehension. Templates can and should be adapted to fit the study plans and needs of prospective participants. Using one of the templates below helps ensure that your consent form includes these elements. This ethical obligation exists for all research-exempt and non-exempt.įederal regulations outline informed consent requirements for non-exempt research, including a list of information participants must receive (i.e., elements of informed consent). Researchers must ensure prospective participants receive information about the study, sufficiently detailed to facilitate a truly informed choice, in a manner that facilitates voluntary consideration of whether to participate. Informed consent is a cornerstone principal of ethical human subjects research.
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