Post-Study Informed Consent Comprehension Assessment
Assesses whether research participants understood key elements of informed consent—study purpose, risks, data handling, and participant rights. Designed for post-study administration to support IRB compliance and iterative improvement of consent materials.
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。
Before starting the study, did you read the consent information provided to you?
- Yes, thoroughly
- Yes, I skimmed it
- I started but did not finish
- No
- Not sure
In your own words, what was the main purpose of the study you participated in?
To the best of your recollection, how were your study data handled?
- Anonymous (no identifiers collected)
- De-identified (coded; no direct identifiers)
- Identifiable (name or contact info attached)
- Not sure
Were you provided with contact details for questions or concerns about the study?
- Yes
- No
- Not sure
The consent information was an appropriate length.
What is your age range?
- 18–24
- 25–34
- 35–44
- 45–54
- 55–64
- 65+
- Prefer not to say
Thank you for completing this survey. Your feedback is invaluable and will help us improve our consent materials and the participant experience in future studies. If you have any questions, please contact the research team using the details provided in your consent form.
Approximately how long did you spend reading the consent information?
- Less than 1 minute
- 1–2 minutes
- 3–5 minutes
- 6–10 minutes
- More than 10 minutes
- I did not read it
How clear was the study's purpose to you before you began?
Which of the following best matches what you recall about how your data may be shared?
- Only the study team could access my data
- The team and approved collaborators could access my data
- De-identified data might be shared publicly (e.g., repositories)
- Data would not be shared beyond the team
- I don't remember
Do you recall being told how to request that your data be deleted or corrected?
- Yes, I remember how
- I was told but don't remember the details
- I don't recall being told
- Not sure
Was any information in the consent materials missing, unclear, or in need of improvement? Please explain.
How do you describe your gender? Select all that apply.
- Woman
- Man
- Non-binary
- Another gender identity
- Prefer not to say
Was this your first time participating in a study with this research team?
- Yes
- No
- Not sure
How clearly were the potential risks of the study explained to you?
What do you recall about how long your data will be retained?
- Only during data analysis
- For several years
- Indefinitely
- I don't remember
I understood that I could withdraw from the study at any time without penalty.
We'd like to understand your experience with the consent process in a bit more depth. An AI moderator will ask you a couple of follow-up questions.
In which region do you currently reside?
- Africa
- Asia
- Europe
- North America
- Oceania
- South America
- Prefer not to say
Based on what you were told, what level of risk did this study pose to you?
- None
- Minimal
- Moderate
- High
- Not sure
How confident are you that your data will be kept confidential as described in the consent information?
I understood that I had the right to ask questions about the study at any point.
Based on your responses in this survey, is there anything else you would like to share about the consent information or your study experience?
What is the highest level of education you have completed?
- Less than high school
- High school or equivalent
- Some college / Associate degree
- Bachelor's degree
- Master's degree
- Doctoral or professional degree
- Prefer not to say
I was clearly informed about any compensation or incentives for participating.
What is your current employment status?
- Employed full-time
- Employed part-time
- Self-employed
- Student
- Not employed
- Retired
- Prefer not to say
To what extent did payment or incentives influence your decision to participate?
- Not at all
- A little
- Somewhat
- A lot
- Prefer not to say
Have you previously participated in academic research at any institution?
- Yes
- No
- Prefer not to say
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
- Directly tests comprehension of purpose, risks, data handling, and rights with dedicated opinion-scale and multiple-choice items rather than just collecting a signature
- Includes an AI follow-up interview that adaptively probes participants' understanding of the consent process in their own words, going beyond fixed-choice recall questions
- Open-text items capture verbatim participant explanations of study purpose and flag any consent materials that were unclear or incomplete, directly supporting iterative consent-form improvement
- Captures prior research experience and demographic context so IRBs can check whether comprehension varies across participant subgroups
Jotform
Research Informed Consent Form TemplateThis is a pre-study consent FORM used to obtain and document a participant's agreement to join a study, not a post-study instrument for checking whether they actually understood what they agreed to. It's a fielding-ready static form, well suited for the consent-collection step but not for measuring comprehension afterward. Teams would need a separate instrument (like this one) to verify understanding and support IRB reporting.
優れている点
- Quick to deploy for the consent-signing step of a study
- Customizable form fields and layout typical of Jotform's builder
- Likely supports e-signature/acknowledgment capture for compliance records
物足りない点
- Collects a signed agreement rather than testing whether participants understood purpose, risks, data handling, or rights
- Static form with no adaptive follow-up questioning or voice AI interview to probe understanding
- No automated per-response quality scoring or generated comprehension report for IRB review
よくあるご質問
「Post-Study Informed Consent Comprehension Assessment」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29問含まれており、最初の設問は次のとおりです:「Welcome, and thank you for taking part in our study. This short survey (approximately 13 minutes) asks about your experi…」・「Before starting the study, did you read the consent information provided to you?」・「In your own words, what was the main purpose of the study you participated in?」。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、29問を約12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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