Informed Consent Form Template: JotformJotform

Consent Forms

Informed Consent Form Template

General informed consent with participant details, a description of the procedure or study, risks and benefits, voluntary participation and the right to withdraw, and a dated signature with a witness line.

Available online on

  • Free PDF and Word downloads for offline use
  • Fillable fields you can customize for your business
  • Share a link or print copies for in-person sign-ups
  • Ready-made online forms on popular form builders

Last updated July 18, 2026. Reviewed by the Online Signature Forms team.

About this template

An Informed Consent Form confirms that a person understands what they are agreeing to — a procedure, a research study, or a service — and takes part voluntarily. Researchers, clinics, wellness providers, and any organization that needs documented, informed agreement use one so there is a signed record that the participant knew the risks and benefits and chose to proceed. Typical fields include the participant's details, a description of the procedure or study, a statement of risks and benefits, a note that participation is voluntary and can be withdrawn, an acknowledgment checkbox, and a dated signature — with a witness line for added assurance.

The signature is the point of the document: informed consent means the person agreed with a real understanding of what was involved, not just a quick nod. This layout keeps the description and the risks and benefits readable, states the right to withdraw, places an acknowledgment checkbox above the signature, and adds a witness line. To be clear, this is a general-purpose layout with the sections most consent forms need — not legal or medical advice. Have the appropriate professional, such as an ethics board or attorney, review the wording before you rely on it.

How teams use this form

A university research team uses it to enroll study participants, documenting that each person understood the study and consented freely. A cosmetic clinic uses it before an elective treatment so the client acknowledges the risks. A wellness studio uses it before a new service, and a nonprofit uses it before interviewing people for a published report. The common thread: nothing proceeds until the participant has signed an informed, voluntary agreement.

Customize the statement before signing

Open the Word (DOCX) download to describe your specific procedure or study, list the real risks and benefits, and set out how a participant withdraws and what happens to their data if they do. Add your organization name and logo, and expand the witness or guardian details if your context calls for them. The fillable PDF suits signing on paper or on a device; keep the checkbox and signature block intact so the consent is complete.

Common mistakes to avoid

Do not gloss over the risks — informed consent depends on the participant genuinely understanding them, so state them plainly. Do not forget to say that participation is voluntary and can be withdrawn without penalty. And do not treat a signature as valid if the person did not have a real chance to read and ask questions. Give the participant a copy so they keep a record of what they agreed to.

Example scenario

A research assistant enrolls a volunteer in a short study. She walks through the description, the risks and benefits, and the note that the volunteer can stop at any time with no consequence. The volunteer reads the form, ticks the acknowledgment box, and signs and dates it; the assistant signs the witness line to confirm the consent was given freely. Both keep a copy, and the signed form goes into the study records.

Choosing PDF or Word

This page provides a printable fillable PDF and an editable Word (DOCX) file. Use the Word file when you need to describe the procedure or study, edit the risk and withdrawal language, or adjust the witness line before printing, and the PDF when the text is set and you just need to fill and sign. Both include the acknowledgment checkbox and a dated signature block with a witness line so the consent is ready to use.

Typical fields

  • Participant name
  • Date of birth
  • Description of procedure, study, or service
  • Risks and benefits
  • Voluntary participation and right to withdraw
  • Acknowledgment checkbox
  • Participant signature and date
  • Witness name, signature, and date

Best for

  • Research studies and trials
  • Clinics and elective procedures
  • Wellness and treatment services
  • Any documented, voluntary agreement

When to use PDF vs online

Use the PDF or Word download for in-person sign-ups, fax, or email attachments. Choose an online form when you need automatic notifications, payment integrations, or a shareable link for customers.

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Common questions about this form

The participant's details, a clear description of the procedure or study, a statement of the risks and benefits, a note that participation is voluntary and can be withdrawn, an acknowledgment checkbox, and a dated signature — with a witness line. This template includes all of those.

The person must understand what they are agreeing to — the procedure, the risks and benefits, and their right to withdraw — and agree freely without pressure. Stating those plainly and giving time for questions is what separates informed consent from a rushed signature.

It is a general-purpose layout, not legal or medical advice. Requirements vary by context — research studies, for example, often need ethics-board approval — so have the appropriate professional review the wording before you rely on it. For a minor, add a parent or guardian signature.