Research Informed Consent & Enrollment
A complete consent flow for research studies: plain-language study information, granular consent statements with a comprehension check, signature capture, and contact enrollment. Built for IRB-style requirements — participants confirm they understand, not just that they scrolled.
設問の例
テンプレートの内容をプレビューできます。すべての設問は公開前に自由に編集できます。
STUDY INFORMATION — Purpose: [describe the study purpose in plain language]. What participation involves: [sessions, duration, recordings]. Risks and discomforts: [describe honestly]. Benefits and compensation: [amount and conditions]. Data handling: your data is stored securely, reported only in aggregate or pseudonymized form, and retained for [period]. Contact: [researcher name, institution, email]. This study has been approved by [IRB/ethics board reference].
Please review and confirm your consent to participate.
Recording consent (required for sessions that are recorded).
Quick comprehension check: what happens if you decide to stop participating halfway through the study?
- I can withdraw at any time, no reason needed
- I must complete the study once enrolled
- I can only withdraw with the sponsor's approval
Please type your full legal name.
Please sign below to record your consent.
Today's date:
Email address for study communications:
Thank you — your consent is recorded and a copy of this form will be sent to your email. Welcome to the study; you'll hear from the research team with next steps.
含まれる機能
AIによる深掘り
自由回答に合わせてAIが追加で質問し、固定のフォームでは拾えない具体的な内容を引き出します。
注意確認設問
急いだ回答や質の低い回答者を除外する仕組みを標準で備えています。
AIが作成する設問文
文言、設問の順序、条件分岐をAIが調査の目的に合わせて作成します。
自動レポート
回答が集まると、テーマ、引用、わかりやすい要約が自動で作成されます。
他ツールとの比較
ほかのアンケートツールで最も近いテンプレートを調べました。それぞれの優れている点と、このテンプレートがさらに踏み込んでいる点をまとめています。
このテンプレートを選ぶ理由
- A comprehension check verifies participants understood withdrawal rights — consent beyond scrolled-past text
- Granular consent statements separate participation from recording and quote usage, each individually confirmable
- Signature, date, and email receipt complete an IRB-style enrollment record in one flow
- Plain-language structure with clearly marked slots for study details, risks, and ethics-board references
Jotform
Research Informed Consent Form TemplatePurpose-built research consent form with participant/representative/parent-guardian/witness name fields, a consent & authorization block, e-signature widgets, up to three researcher signature blocks, and conditional logic. Strong on signature capture and roles, but it is a standalone form, not a consent gate that conditionally admits/blocks entry to the actual research instrument.
優れている点
- Dedicated signature capture for participants, representatives, guardians, witnesses, and up to three researchers
- E-signature widgets plus conditional logic to ensure required information is captured
- Role selection (participant vs. legal representative vs. guardian) built in
- Framed around collecting, managing, and protecting consent data for human-subjects research
物足りない点
- Consent lives as its own form; no native gating that routes non-consenting respondents away from the study and admits consenting ones into the same instrument
- No attention/comprehension check to confirm the participant actually understood key risk elements before signing
- No adaptive follow-up (e.g., clarifying questions when a participant hesitates on a specific authorization)
- No auto-generated participant-facing PDF receipt described beyond standard form submission
Qualtrics
Building a Consent Form (support guide)Official Qualtrics guide (not a one-click template) for building a research consent gate using skip logic for simple studies or Survey Flow branch logic for complex designs, plus an insertable downloadable file to review before consenting. Covers the consent-gating pattern well, but the core walkthrough is a yes/no consent question and does not cover digital signature capture.
優れている点
- Teaches the consent-gate pattern: skip logic (simple) or Survey Flow branch logic (complex) to end the survey for non-consenting respondents
- Supports inserting a downloadable consent document for review before responding
- Addresses GDPR/personal-data considerations in its FAQ
- Flexible enough for advanced multi-condition study designs
物足りない点
- Guide covers only a yes/no consent question; digital signature capture is not part of this walkthrough (it must be added separately)
- Requires manually wiring skip/branch logic; no packaged consent+signature question type
- No comprehension/attention check to verify understanding before consenting
- No adaptive follow-up or plain-language explainer surfaced to hesitant participants
よくあるご質問
「Research Informed Consent & Enrollment」テンプレートにはどのような設問が含まれていますか?
すぐに使える設問が10問含まれており、最初の設問は次のとおりです:「Before joining the study, please review what participation involves. Take your time — a researcher's contact details are…」・「STUDY INFORMATION — Purpose: [describe the study purpose in plain language]. What participation involves: [sessions, dur…」・「Please review and confirm your consent to participate.」。すべての設問は上でプレビューでき、自由に編集できます。
このアンケートの回答にはどのくらい時間がかかりますか?
回答者は通常、10問を約3分で回答し終えます。
テンプレートは編集できますか?
はい。公開前であれば、すべての設問、選択肢、順序を編集できます。設問の追加や削除のほか、調査の目的に合わせた作り直しをAIエディターに依頼することもできます。
このテンプレートは無料で使えますか?
はい。エディターで開けば、すぐに編集を始められます。お試しにアカウントは不要で、無料プランでアンケートを公開できます。
公開の準備はできましたか?
このテンプレートをエディターで開いてみてください。最初の回答者が目にする前に、すべてを自由に変更できます。
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