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Research Consent Form

Informed consent for a study, covering what the participant is agreeing to, how their data is handled, and their right to withdraw.

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Research Consent Form

Informed consent for a study, covering what the participant is agreeing to, how their data is handled, and their right to withdraw.

About this study

About you

Your consent

Placeholder wording. Replace it with the statements your ethics approval covers, and keep them as separate items so a participant can decline one without declining all of them.

You can take part without agreeing to any of these.

Sign above

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Use this template

Opens in the builder. Nothing is saved until you edit it. Or ask Claude or ChatGPT to build it.

Fields
12 questions
Layout
Classic, every question on one page
Theme
Editorial, switchable in the preview
Updated
10 September 2026

Categories

  • Consent form templates
  • Consent Forms
  • Research Forms
  • Education Forms

Form type

  • Consent and waiver form templates

Ideal for

  • Academic researchers
  • PhD students
  • UX researchers
  • Clinical teams

Best used in

  • Studies
  • Interviews
  • User research

About this template

Informed consent is not one agreement, it is several, and this form treats it that way. The required list covers the things a participant must accept to take part at all. The optional list covers audio recording, quotation and recontact, which are separate asks that plenty of people will decline while still being happy to take part. Bundling them into one tick box is the mistake that makes a consent record worthless when somebody later objects to being quoted.

The study information section is a placeholder and needs replacing before this goes anywhere near a participant. An ethics committee will expect the purpose, the procedure, the risks and a named contact in front of the person signing, not linked from somewhere else, and what they require differs by institution.

The withdrawal statement is the one people most often water down. If a participant can withdraw without giving a reason, say exactly that, and be clear about what happens to data already collected when they do, because that is the question they will actually ask.

Add a page break after the information section if the study sheet is long, so nobody scrolls past it to reach the tick boxes.

Templates are a starting point, not legal or professional advice. Where a form carries consent, medical, or contractual wording, have somebody qualified review it against the rules that apply to you before you publish.

Fields in this template

  • Study title*Short text
  • Lead researcherShort text
  • Full name*Short text
  • Email address*Email
  • Participant number, if you were given oneShort text
  • Are you 18 or over?*Single choice
  • Parent or guardian name, if applicableShort text
  • Please confirm each of the following*Multiple choice
  • Optional permissionsMultiple choice
  • Any questions or conditions you want recordedLong text
  • Signature*Signature
  • Date*Date

Every field can be renamed, reordered, made optional, or removed once the template is open in the builder.

Build this form by asking Claude or ChatGPT

Connect Deoochform to Claude, ChatGPT, or any assistant that supports MCP, then send it the message below. It creates the research consent form from this template in your account and replies with a link. You can ask it to add, remove, or reword questions in the same chat before you share the form.

Make me a form in Deoochform from your Research Consent Form template, then send me the link to share.

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Frequently asked questions

Will an ethics committee accept an online consent form?
Many will, and many have specific requirements about how consent is recorded, stored and withdrawn. A drawn signature with a timestamp is stronger evidence than a single tick box, which is why this template includes one. What no template can tell you is what your own committee requires, so submit the wording you intend to use rather than assuming a generic form will pass.
Why separate the required and optional consent lists?
Because they are different decisions. Taking part in a study and agreeing to be quoted in a publication are not the same commitment, and a participant who wants one but not the other has no way to say so if both sit in the same block. Keeping them apart also means your record shows precisely what each person agreed to.
How do I handle consent for a participant under 18?
A parent or guardian signs, and the form should record that this is what happened. The age question here branches to a guardian name field for exactly that reason. Many committees also expect age appropriate assent from the child alongside the guardian's consent, so check whether yours requires a second form.

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