{"id":231,"date":"2025-11-07T18:48:10","date_gmt":"2025-11-07T18:48:10","guid":{"rendered":"https:\/\/www.smcm.edu\/academic-affairs\/?page_id=231"},"modified":"2026-03-31T17:41:23","modified_gmt":"2026-03-31T17:41:23","slug":"irb","status":"publish","type":"page","link":"https:\/\/www.smcm.edu\/academic-affairs\/irb\/","title":{"rendered":"Institutional Review Board"},"content":{"rendered":"<div id=\"pl-231\"  class=\"panel-layout\" ><div id=\"pg-231-0\"  class=\"panel-grid panel-no-style\" ><div id=\"pgc-231-0-0\"  class=\"panel-grid-cell\" ><div id=\"panel-231-0-0-0\" class=\"so-panel widget widget_text panel-first-child panel-last-child\" data-index=\"0\" >\t\t\t<div class=\"textwidget\"><p>The Institutional Review Board (IRB) evaluates research using human participants that is conducted by members of the St. Mary\u2019s College of Maryland community. The IRB operates under the guidelines enacted by the Office of Human Research Protection, a branch of the U.S. government\u2019s Food and Drug Administration.<\/p>\n<p>The IRB reviews all human subject research including proposed changes in previously approved human subject research. The IRB has the authority to approve, require modification in, or disapprove all human subject research.<\/p>\n<p>The IRB also has the authority to suspend or terminate the approval of previously approved human subject research that is not being conducted in accordance with the IRB\u2019s requirements or that has been associated with unexpected, serious harm to subjects.<\/p>\n<\/div>\n\t\t<\/div><\/div><div id=\"pgc-231-0-1\"  class=\"panel-grid-cell\" ><div id=\"panel-231-0-1-0\" class=\"so-panel widget widget_media_image panel-first-child panel-last-child\" data-index=\"1\" ><img loading=\"lazy\" decoding=\"async\" width=\"1232\" height=\"820\" src=\"https:\/\/www.smcm.edu\/app\/uploads\/sites\/158\/2025\/11\/discuss.jpg\" class=\"image wp-image-246  attachment-full size-full\" alt=\"A group of people are seated in a circle having a discussion in a sunlit room with large windows and wooden chairs.\" style=\"max-width: 100%; height: auto;\" srcset=\"https:\/\/www.smcm.edu\/app\/uploads\/sites\/158\/2025\/11\/discuss.jpg 1232w, https:\/\/www.smcm.edu\/app\/uploads\/sites\/158\/2025\/11\/discuss-300x200.jpg 300w, https:\/\/www.smcm.edu\/app\/uploads\/sites\/158\/2025\/11\/discuss-1024x682.jpg 1024w, https:\/\/www.smcm.edu\/app\/uploads\/sites\/158\/2025\/11\/discuss-768x511.jpg 768w, https:\/\/www.smcm.edu\/app\/uploads\/sites\/158\/2025\/11\/discuss-272x182.jpg 272w\" sizes=\"auto, (max-width: 1232px) 100vw, 1232px\" \/><\/div><\/div><\/div><div id=\"pg-231-1\"  class=\"panel-grid panel-no-style\" ><div id=\"pgc-231-1-0\"  class=\"panel-grid-cell\" ><div id=\"panel-231-1-0-0\" class=\"so-panel widget widget_smcm-gold-buttons panel-first-child panel-last-child\" data-index=\"2\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-gold-buttons so-widget-smcm-gold-buttons-default-d75171398898-231\"\n\t\t\t\n\t\t><nav class=\"smcm-gold-buttons\"><ul><li><div class=\"smcm-gb-item\"><a href=\"https:\/\/inside.smcm.edu\/directory\/institutional-review-board\"><div class=\"smcm-gb-label-wrapper\">Meet the Members<\/div><div class=\"smcm-gb-icon-wrapper\"><i class=\"fa-solid fa-angles-right smcm-gb-linktype\" aria-hidden=\"true\"><\/i><\/div><\/a><\/div><div class=\"smcm-gb-item\"><a href=\"#rmp\"><div class=\"smcm-gb-label-wrapper\">Research Misconduct Policy<\/div><div class=\"smcm-gb-icon-wrapper\"><i class=\"fa-solid fa-angles-down smcm-gb-linktype\" aria-hidden=\"true\"><\/i><\/div><\/a><\/div><\/li><li><div class=\"smcm-gb-item\"><a href=\"#faq\"><div class=\"smcm-gb-label-wrapper\">Frequently Asked Questions<\/div><div class=\"smcm-gb-icon-wrapper\"><i class=\"fa-solid fa-angles-down smcm-gb-linktype\" aria-hidden=\"true\"><\/i><\/div><\/a><\/div><div class=\"smcm-gb-item\"><a href=\"https:\/\/www.smcm.edu\/academic-affairs\/irb\/forms\/\"><div class=\"smcm-gb-label-wrapper\">Forms<\/div><div class=\"smcm-gb-icon-wrapper\"><i class=\"fa-solid fa-angles-right smcm-gb-linktype\" aria-hidden=\"true\"><\/i><\/div><\/a><\/div><\/li><\/ul><\/nav><\/div><\/div><\/div><\/div><div id=\"pg-231-2\"  class=\"panel-grid panel-no-style\" ><div id=\"pgc-231-2-0\"  class=\"panel-grid-cell\" ><div id=\"panel-231-2-0-0\" class=\"so-panel widget widget_smcm-title panel-first-child\" data-index=\"3\" ><div id=\"rmp\" class=\"panel-widget-style panel-widget-style-for-231-2-0-0\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-title so-widget-smcm-title-base\"\n\t\t\t\n\t\t><h2 class=\"smcm-section-title navy\" style=\"\"><strong>Research<\/strong> Misconduct Policy<\/h2><\/div><\/div><\/div><div id=\"panel-231-2-0-1\" class=\"so-panel widget widget_text panel-last-child\" data-index=\"4\" >\t\t\t<div class=\"textwidget\"><div class=\"gmail_default\">The integrity of research at SMCM is of high importance. The <a href=\"https:\/\/www.smcm.edu\/app\/uploads\/sites\/158\/2026\/03\/Scientific-Misconduct-Policy-1.pdf\">SMCM Scientific Research Misconduct Policy (PDF)<\/a> addresses both what constitutes research conduct and how allegations of misconduct will be investigated.<\/div>\n<\/div>\n\t\t<\/div><\/div><\/div><div id=\"pg-231-3\"  class=\"panel-grid panel-no-style\" ><div id=\"pgc-231-3-0\"  class=\"panel-grid-cell\" ><div id=\"panel-231-3-0-0\" class=\"so-panel widget widget_smcm-title panel-first-child\" data-index=\"5\" ><div id=\"faq\" class=\"panel-widget-style panel-widget-style-for-231-3-0-0\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-title so-widget-smcm-title-base\"\n\t\t\t\n\t\t><h2 class=\"smcm-section-title navy\" style=\"\"><strong>Frequently <\/strong>Asked Questions<\/h2><\/div><\/div><\/div><div id=\"panel-231-3-0-1\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"6\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>What research projects need to be approved by the IRB?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>Research involving human subjects needs to be approved by the IRB. \u201cResearch\u201d is defined as \u201ca systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge.\u201d<\/p>\n<p>A \u201chuman subject\u201d is defined as \u201ca living individual about whom an investigator conducting research obtains information or biopspecimens through intervention or interaction with the individual, and uses, studies or analyzes the information or biospecimens;\u00a0or\u00a0obtains, uses, studies, analyzes or generates identifiable private information or identifiable biospecimens.\u201d<\/p>\n<p>Revised federal regulations in effect as of 2018 indicate that the following activities are\u00a0not\u00a0deemed to be research under these regulations and therefore do\u00a0not\u00a0need to undergo IRB review:\u00a0 \u201cScholarly and journalistic activities (e.g.,\u00a0oral history, journalism, biography, literary criticism, legal research, and historical scholarship), including the collection and use of information, that focus directly on the specific individuals about whom the information is collected.\u201d<\/p>\n<p>If you are not sure if your research requires IRB review, please consult with the IRB by emailing a short description of your project (its purpose and your data collection procedures) to\u00a0<a href=\"mailto:irb@smcm.edu\">irb@smcm.edu<\/a>.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-2\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"7\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>Why have you told me that my project needs to be reviewed?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>The St. Mary\u2019s College Institutional Review Board formulated the following two guidelines for the review of research involving human subjects conducted at St. Mary\u2019s College, or conducted by St. Mary\u2019s College faculty or professional staff (February 7, 1986).<\/p>\n<ol>\n<li>All research involving human subjects must receive an ethics review by the IRB if the subjects are being recruited from outside the instructor\u2019s classroom and the research project is not an in-class demonstration.<\/li>\n<li>An evaluation of the ethics involved in in-class research demonstrations and experiments remains entrusted with the individual instructor.<\/li>\n<\/ol>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-3\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"8\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>What is an expedited review?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>An expedited review applies to certain kinds of research involving no more than minimal risk, and to minor changes in approved research. An expedited review is carried out by the IRB chairperson or by one or more experienced reviewers designated by the chairperson from among members of the IRB. If there is sufficient concern about a proposal during an expedited review, the proposal will be reviewed by the full IRB before a decision is made. For additional information on expedited reviews, see the <a href=\"https:\/\/www.hhs.gov\/ohrp\/regulations-and-policy\/guidance\/categories-of-research-expedited-review-procedure-1998\/index.html\">OHRP\u00a0website<\/a>.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-4\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"9\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>How do I get my project reviewed by the IRB?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>The eIRB form, instructions for completing the eIRB form, and templates for informed consent can all be found on this webpage.\u00a0 The completed eIRB form should be emailed to <a href=\"mailto:irb@smcm.edu\">irb@smcm.edu<\/a> for review.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-5\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"10\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>Where can I obtain the IRB form and instructions?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>The IRB form, instructions for completing the form, and templates for informed consent can be found on the IRB webpage.\u00a0 The completed form should be emailed to <a href=\"mailto:irb@smcm.edu\">irb@smcm.edu<\/a> for review.\u00a0 Questions about completing the form can be sent to <a href=\"mailto:irb@smcm.edu\">irb@smcm.edu<\/a>, but most commonly asked questions are answered in the instructions document.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-6\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"11\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>How do I submit an IRB proposal?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>To submit an IRB proposal, complete the IRB form by editing the Microsoft Word file.<\/p>\n<p><strong>Important<\/strong>:\u00a0Make sure to include any appendixes (e.g., consent form(s), debriefing statements, copies of surveys, list of interview questions, and other materials being presented to participants) at the end of the file, include a page break between each appendix and attach\u00a0<strong>one<\/strong>\u00a0file to an e-mail message and send it to\u00a0<a href=\"mailto:irb@smcm.edu\">irb@smcm.edu<\/a>. Your IRB proposal is NOT complete if it does not contain your consent form(s) and other relevant information!<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-7\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"12\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>What kinds of ethical issues does the IRB consider?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>The SMCM IRB reviews projects following federal guidelines for protecting human subjects (The Revised Common Rule, Code of Federal Regulations).\u00a0\u00a0<a href=\"https:\/\/www.ecfr.gov\/current\/title-45\/subtitle-A\/subchapter-A\/part-46\/subpart-A\/section-46.111\">You can explore the full guidelines we use for review<\/a>.<\/p>\n<ul>\n<li>Criteria for IRB approval of research:\n<ul>\n<li>risks to subjects are minimized;<\/li>\n<li>risks are reasonable in relation to anticipated benefits;<\/li>\n<li>selection of subjects is equitable;<\/li>\n<li>informed consent is sought from each subject;<\/li>\n<li>informed consent is appropriately documented.<\/li>\n<\/ul>\n<\/li>\n<li>Additional criteria where appropriate:\n<ul>\n<li>data collection is monitored to ensure subject safety;<\/li>\n<li>privacy and confidentiality of subjects is protected;<\/li>\n<li>additional safeguards are included for vulnerable populations<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-8\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"13\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>What is informed consent?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>Informed consent refers to the voluntary choice of an individual to participate in research based on an accurate and complete understanding of its purposes, procedures, risks, benefits, alternatives, and any other factors that may affect a person\u2019s decision to participate. Informed consent is typically gathered by having participants sign a hard copy consent form or indicate their consent in an online format. Participants under the age of 18 must have the consent of a parent or guardian and must also give their own assent to participate.\u00a0 Templates for SMCM consent forms are available and their use is encouraged to make sure all required elements of consent are present in the consent form.\u00a0 Information about informed consent can be found from the <a href=\"https:\/\/www.ecfr.gov\/cgi-bin\/text-idx?SID=91137a43527512a23d10a2d56603fdd2&amp;mc=true&amp;node=se45.1.46_1116&amp;rgn=div8\">federal guidelines.<\/a><\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-9\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"14\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>Does the IRB need to review projects that have small revisions?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>Yes, any substantive revision to a project must be reviewed by the IRB.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-10\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"15\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>How long does it take the IRB to review a proposal?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>The IRB is committed to making quick decisions. In most cases (i.e., expedited proposals), a decision will be returned (via electronic mail) to the investigators within 3-5 working days (weekends and holidays are excluded), however during peak submission times it may take longer. Proposals submitted during summer months and proposals submitted on paper rather than electronically generally require a longer review time. Additionally, if members of the IRB have questions for the researchers, then the review time may be lengthened. Although the IRB has been successful in meeting the goal of 3-5 working days, there is no guarantee. Therefore, investigators should plan ahead and submit IRB proposals early in order to ensure an early initiation of approved projects.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-11\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"16\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>What if some unforeseen risks emerge as the research is being conducted?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>Any unforeseen risks or negative response to the research must be reported to the IRB immediately.\u00a0 The researcher should temporarily suspend data collection and promptly inform the chair of the IRB by sending an e-mail to\u00a0<a href=\"mailto:irb@smcm.edu\">irb@smcm.edu<\/a>\u00a0and directly to the current Chair.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-12\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"17\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>What if I\u2019m collaborating with a researcher at another institution?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>If a project involves more than one institution, researchers must typically rely on the approval of a single IRB. The chosen IRB is responsible for monitoring the project\u2019s ethical compliance. We recommend researchers talk with collaborators about which IRB they want to use. We also recommend considering which collaborator will be most responsible for data collection and if the collaborator\u2019s institution has a preferred process for designating a single IRB (the SMCM IRB can be either the \u201creviewing\u201d IRB or the \u201crelying\u201d IRB). Multi-site projects typically require a reliance\/authorization agreement form provided by the \u201creviewing\u201d IRB. We recommend consulting with an IRB chair early in the process of collaborative work.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-13\" class=\"so-panel widget widget_smcm-accordion\" data-index=\"18\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>Do I need IRB approval for research conducted in classes?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>Class-driven projects that meet the definition of research and recruit participants beyond those enrolled in the course require IRB approval. If students are conducting research with similar projects that pose no known risk (e.g., all participants will view an image of an optical illusion and then answer three questions about what they saw), it may be prudent for the instructor to submit one IRB proposal describing the general protocol. The instructor can discuss the project with an IRB chair in advance to help prevent unnecessary delays in review.<\/p>\n<p>If a class-based IRB proposal cannot be submitted by the instructor (e.g., because of the nature of the projects being very different from one another), individual project IRB submissions by students are recommended. We recommend that the instructor carefully review student IRB submissions to be sure they are complete and all ethical concerns are addressed before the student(s) submit them to the IRB. We recommend that class-driven project submissions (as well as student SMP submissions) be sent to the IRB as early as possible (at least one month but no later than two weeks before the planned data collection) to allow sufficient time for possible revisions.<\/p>\n<\/div><\/div><\/div><\/div><\/div><div id=\"panel-231-3-0-14\" class=\"so-panel widget widget_smcm-accordion panel-last-child\" data-index=\"19\" ><div\n\t\t\t\n\t\t\tclass=\"so-widget-smcm-accordion so-widget-smcm-accordion-base\"\n\t\t\t\n\t\t><div class=\"smcm-accordion  navy\"><div class=\"title-container\"><h3>What should I do if I have other questions about IRB procedures?<\/h3><i class=\"fa-solid fa-plus open-close\" ><\/i><\/div><div class=\"smcm-accordion-content\"> <div class=\"smcm-ac-content-wrapper\"><p>Send an email to\u00a0<a href=\"mailto:irb@smcm.edu\">irb@smcm.edu<\/a>\u00a0and we will respond to your questions as quickly as possible!\u00a0 If you have questions about completing the IRB submission form, be sure to review the Instructions document on the Forms page for further information about how to complete the forms.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"<p>The Institutional Review Board (IRB) evaluates research using human participants that is conducted by members of the St. Mary\u2019s College of Maryland community. The IRB operates under the guidelines enacted by the Office of Human Research Protection, a branch of the U.S. government\u2019s Food and Drug Administration. The IRB reviews all human subject research including<a class=\"tribe-events-read-more\" href=\"https:\/\/www.smcm.edu\/academic-affairs\/irb\/\" rel=\"bookmark\" > Find out more &raquo;<\/a><\/p>\n","protected":false},"author":234,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"full-width-content","footnotes":""},"class_list":{"0":"post-231","1":"page","2":"type-page","3":"status-publish","5":"entry"},"acf":[],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/www.smcm.edu\/academic-affairs\/wp-json\/wp\/v2\/pages\/231","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.smcm.edu\/academic-affairs\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.smcm.edu\/academic-affairs\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.smcm.edu\/academic-affairs\/wp-json\/wp\/v2\/users\/234"}],"replies":[{"embeddable":true,"href":"https:\/\/www.smcm.edu\/academic-affairs\/wp-json\/wp\/v2\/comments?post=231"}],"version-history":[{"count":3,"href":"https:\/\/www.smcm.edu\/academic-affairs\/wp-json\/wp\/v2\/pages\/231\/revisions"}],"predecessor-version":[{"id":328,"href":"https:\/\/www.smcm.edu\/academic-affairs\/wp-json\/wp\/v2\/pages\/231\/revisions\/328"}],"wp:attachment":[{"href":"https:\/\/www.smcm.edu\/academic-affairs\/wp-json\/wp\/v2\/media?parent=231"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}