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Consent documents at GCU: the required elements, the reading level, and the version that has to match
Grand Canyon University does not ask you to write a consent document. It asks you to complete one — a current template whose section headings, required sentences and closing block are not yours to rearrange, filled in with the study your proposal already describes. Two things then decide whether the board can use the page: whether an ordinary reader could act on it, and whether it says precisely what the application and the recruitment material say. Most returns at this exhibit are failures of the second kind.
The short answer
Use GCU's current consent template without altering its language or deleting sections, complete every prompt, meet the reading level and attach the readability evidence, and make the eligibility criteria and activities identical to the application and the recruitment material.
Why does GCU treat the template as the document?
Because the template carries the federal elements already. Consent under 45 CFR 46.116 opens with the "key information" — placed first and kept short, so a decision can be weighed before the detail arrives; it is written in language the reader actually understands; and it carries no exculpatory wording that appears to sign away anyone's rights. GCU's template arranges those obligations into headings and fills the gaps with instructional prompts. Rewrite the structure and you are not improving a document — you are dismantling the part that already satisfies the rule.
So the template's housekeeping instructions are substantive. Its coloured prompts are deleted before filing. Its required sentences stay as written. The finished page is uniform black type at readable size, with tracked changes accepted and removed rather than hidden from view, because hidden markup reappears once the document is uploaded to GCU's portal. GCU's own warning is that a consent document in the wrong template, with sections altered or deleted, or carrying tracked changes or spelling errors, is sent back for revision before the substance is reached. That is a return earned on formatting, and it is entirely avoidable.
One line in GCU's guidance is worth keeping in view while you draft: signing the consent document is not a research activity. It is what has to happen before any research activity, which is why an online survey has to open on the approved consent page — not on a welcome screen, not on the first question — and why a consent conversation that follows the first interview question is not a consent conversation at all.
What has to appear in a GCU consent document?
The template moves in a fixed order, and each block answers a question the board will ask on the participant's behalf.
- Introduction. The study title, who you are, the chair supervising the work, the college, and the purpose stated plainly — GCU asks explicitly that the purpose not be pasted from the manuscript and that research vocabulary such as phenomenological or correlational be left out, because the reader is a participant rather than a committee.
- Eligibility. Inclusion and exclusion bulleted exactly as they appear in the application and the recruitment material. GCU's template is emphatic that screening criteria are not a separate category: everything you screen on belongs inside inclusion and exclusion.
- Research activities. What, when, where and how — each activity with its estimated time, its date range, its location, and the platform or method used to collect it. Required demographic questions belong in eligibility; optional ones belong in the activity list. That distinction is small and it is checked.
- Recording. Separate blocks for audio and for video, each naming the tool, stating whether someone can take part while declining to be recorded, describing how identity is protected, and linking the platform's privacy policy.
- Access. A required statement that identifiable data may be viewed by the researcher, the chair, committee members and College of Doctoral Studies reviewers as part of the review process. It is not optional and not editable, because those reviewers must be able to verify the data behind the manuscript.
- Voluntariness and withdrawal. Participation is voluntary, withdrawal carries no penalty, and the document must say how someone withdraws and whether data already collected will be used.
- Risks, benefits and compensation. Foreseeable risks or an explicit statement of none; direct benefits or a plain no — GCU notes that contributing to research and receiving an incentive are not direct benefits; and, where compensation exists, what it is and how and when it arrives.
- Presentation, privacy and data security. Where findings will appear and in what form, followed by the privacy block covered in the data security plan: linkability, identifiers, code lists, storage, retention, destruction and third-party platforms.
- Future research, jurisdiction and contacts. The secondary-use clause where de-identified data may be reused, the California residents' rights block where it applies, and contact routes for the study and for questions about participant rights, which run to GCU's IRB rather than to you.
- The closing block. The participant-rights list, then either a signature line or agreement buttons — never both, and never neither.
How readable does it have to be, and what proof does the board want?
GCU sets a lay reading level and asks for evidence, not assurance. The current consent template asks for plain terms at a ninth-grade level, measured by a Flesch-Kincaid grade score at or below 10.0, with a screenshot of the readability result submitted alongside the document and labelled so the reviewer knows which document it belongs to. The package checklist used on doctoral files words the same test more tightly, asking whether the readability report rates 9.0 or less. Where two GCU documents describe one threshold differently, the one attached to the version of the template you are filing is the one to satisfy — and the current wording is set by GCU's current doctoral handbook or IRB portal.
Lowering a score is a writing task, and GCU's own advice is sound: drop the research vocabulary, prefer active sentences, shorten the complex ones, punctuate bulleted items as sentences, and measure only the narrative — logos, address blocks and signature furniture distort the result. What the number is really testing is whether a person can act on the page. A participant who cannot follow the activities cannot meaningfully agree to them, and no signature repairs that.
| Section | What the board is reading for | The common failure |
|---|---|---|
| Eligibility | The same inclusion and exclusion criteria as the application and recruitment | A criterion tightened in one document and not the others |
| Activities | Every activity, with time, place, mode and date range | A follow-up session that exists in the procedures but not here |
| Privacy and data security | One account of identifiers, storage, access and destruction | Coding described one way here and another way in the application |
| The closing block | Signature line for confidential contact, buttons for an anonymous survey | Both retained, or the wrong one left standing after editing |
Signature, buttons, or neither?
Documentation is a separate decision from consent itself. Under 45 CFR 46.117 consent is normally documented by a written form the board has approved and the participant signs, including electronically; a board may also waive that signature in defined circumstances — most usefully when the signed page would itself become the only record tying a person to the study, and the chief risk in the design is a confidentiality breach.
GCU translates that into a practical fork at the end of the template. A study with direct, identifiable contact — interviews, focus groups, recordings, anything the researcher can attribute — is confidential, and keeps the signature line. A genuinely anonymous online survey keeps the agreement and refusal buttons instead and loses the signature block. The package checklist inspects exactly this, item by item, because an editing pass that leaves both endings in place tells the board the researcher has not settled which kind of study this is. Minors bring a third layer: assent alongside parental permission, on GCU's own assent and parental consent templates.
Which version wins when the documents disagree?
None of them. The board does not choose between your documents; it returns the file. That is why version-matching is a discipline rather than a proofreading step, and why it starts upstream: the consent document is written against the proposal as academic quality review approved it, alongside the application and the recruitment material, so that the three of them are drafted as one act. Change a criterion after that and it changes in every document at once, or you have re-created the drift the board is looking for.
The practical test is simple enough to run on a Sunday afternoon. Put the eligibility bullets from the consent document next to the eligibility bullets in the recruitment material and the application, and read them aloud. Then do the same with the activity lists, then with the site authorization letter's list of what the site permits. If any two lists differ by a word that changes meaning, you have found what the reviewer would have found. The wider manifest is set out in the exhibits checklist, and the participant-facing half of the pair is covered in recruitment materials as filed.
How this desk handles it
We build the consent document with the application and the recruitment material in the same sitting, from the approved proposal rather than from an earlier draft, and we treat the template's fixed language as fixed. Reading level is measured on the narrative and evidenced the way GCU asks. The closing block is chosen from the design, not from habit. Then the whole set is read the way a reviewer reads it: any two documents, side by side, saying one thing. Filing and every reply to the board afterwards sit on this desk too, as how it works sets out — the study stays yours, and the determination stays the board's.
What to do next
If your consent document was drafted before your proposal settled, it is probably describing a slightly older study — and that is the version a reviewer will compare against everything else. Send it through the free application review with your approved proposal, and you will get a written reading of what matches, what has drifted, and what the current template expects that an older one did not. Where the honest reading is that your document is already fit to file, we say so plainly. The FAQ covers what follows.
Sources
- Grand Canyon University, Informed Consent template for doctoral candidates (College of Doctoral Studies, modified January 2026) — research.gcu.edu (Informed Consent template)
- Grand Canyon University, IRB Package Checklist for doctoral files — research.gcu.edu (IRB Package Checklist)
- Grand Canyon University, IRB forms, templates, assent and parental consent documents — research.gcu.edu/irb
- Grand Canyon University, IRB Handbook, informed consent and assent sections — research.gcu.edu (IRB Handbook)
- Grand Canyon University, Steps to Prepare IRB Application — research.gcu.edu/steps-to-prepare-irb-application
- 45 CFR 46.116 — what consent must disclose, and the plain-language rule — Legal Information Institute (45 CFR 46.116)
- 45 CFR 46.117 — documenting consent, and when a signature may be waived — Legal Information Institute (45 CFR 46.117)
GCU revises its templates and its portal instructions. Where anything on this page departs from GCU's current doctoral handbook or IRB portal, GCU's own material is what counts. This practice is independent of Grand Canyon University.