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eConsent Clarity & Usability Assessment for Clinical Trials

Evaluates patient comprehension, usability, and decision confidence with electronic informed consent (eConsent) in clinical trials. Designed for post-consent administration to identify barriers and improve the consent experience.

What's Included

AI-Powered Questions

Intelligent follow-up questions based on responses

Automated Analysis

Real-time sentiment and insight detection

Smart Distribution

Target the right audience automatically

Detailed Reports

Comprehensive insights and recommendations

Template Overview

25

Questions

AI-Powered

Smart Analysis

Ready-to-Use

Launch in Minutes

This professionally designed survey template helps you gather valuable insights with intelligent question flow and automated analysis.

Sample Survey Items

Q1
Chat Message
Welcome to this survey about your experience with electronic informed consent (eConsent) in a clinical trial. This survey takes approximately 7–9 minutes to complete. Your participation is entirely voluntary, and you may stop at any time. There are no right or wrong answers — we are interested in your honest opinions. All responses are confidential and will be reported only in aggregate to improve future eConsent processes. No individual responses will be shared with your study team or affect your clinical trial participation in any way. By continuing, you agree to participate in this survey.
Q2
Dropdown
When did you most recently complete an electronic informed consent (eConsent) process for a clinical trial?
  • Within the last month
  • 1–3 months ago
  • 4–6 months ago
  • 7–12 months ago
  • More than 12 months ago
  • I have not completed an eConsent
Q3
Multiple Choice
Which device(s) did you use to review or complete the eConsent? Select all that apply.
  • Smartphone
  • Tablet
  • Laptop
  • Desktop computer
  • Clinic-provided shared device
  • Someone assisted by reading it to me
  • Other
Q4
Multiple Choice
Where did you complete most of the eConsent process?
  • At the clinic with staff present
  • At home or outside the clinic
  • A mix of clinic and home
  • Other
  • Not sure
Q5
Dropdown
Approximately how long did it take you to review and complete the eConsent, including reading?
  • Less than 5 minutes
  • 5–10 minutes
  • 11–20 minutes
  • 21–30 minutes
  • 31–45 minutes
  • More than 45 minutes
  • I don't remember
Q6
Opinion Scale
How clear was the eConsent in explaining the purpose and goals of the study?
Range: 1 7
Min: Not at all clearMid: NeutralMax: Extremely clear
Q7
Opinion Scale
How clear was the eConsent in explaining the potential risks and side effects?
Range: 1 7
Min: Not at all clearMid: NeutralMax: Extremely clear
Q8
Opinion Scale
How clear was the eConsent in explaining how your personal data will be used and protected?
Range: 1 7
Min: Not at all clearMid: NeutralMax: Extremely clear
Q9
Opinion Scale
How clear was the eConsent in explaining your right to withdraw from the study at any time?
Range: 1 7
Min: Not at all clearMid: NeutralMax: Extremely clear
Q10
Opinion Scale
How clear was the eConsent in explaining what procedures and visits are involved?
Range: 1 7
Min: Not at all clearMid: NeutralMax: Extremely clear
Q11
Opinion Scale
Overall, how easy was the eConsent to understand?
Range: 1 7
Min: Very difficult to understandMid: NeutralMax: Very easy to understand
Q12
Multiple Choice
Which of the following features, if any, did you use while reviewing the eConsent? Select all that apply.
  • Search or glossary for terms
  • Short informational videos
  • Illustrations or diagrams
  • Inline definitions next to terms
  • Text-to-speech or screen reader
  • Translation to another language
  • Ability to enlarge text
  • I did not use any of these features
Q13
Opinion Scale
How would you rate the overall layout and readability of the eConsent?
Range: 1 7
Min: Very poorMid: NeutralMax: Excellent
Q14
Ranking
If anything made the eConsent harder to understand, please rank the factors below from biggest barrier to smallest. Skip this question if none applied to you.
Drag to order (top = most important)
  1. Medical jargon or technical language
  2. Length of the document
  3. Small text or screen size
  4. Too many steps or screens
  5. Distractions or fatigue
  6. English is not my primary language
  7. Internet or device issues
Q15
Multiple Choice
Before making your participation decision, were your questions about the study adequately answered?
  • I had no questions
  • Yes, by study staff
  • Yes, by the eConsent materials
  • Partly
  • No
Q16
Opinion Scale
How confident were you in your decision about participating after reviewing the eConsent?
Range: 1 7
Min: Not at all confidentMid: NeutralMax: Extremely confident
Q17
Long Text
Based on your experience, what would make the eConsent process clearer or easier? Please share any additional thoughts.
Max chars
Q18
AI Interview
We'd like to explore your eConsent experience in a bit more depth. An AI moderator will ask you a couple of follow-up questions based on your responses.
AI InterviewLength: 2Personality: [Object Object]Mode: Fast
Reference questions: 6
Q19
Multiple Choice
What is your age group?
  • 18–24
  • 25–34
  • 35–44
  • 45–54
  • 55–64
  • 65–74
  • 75+
  • Prefer not to say
Q20
Multiple Choice
How do you describe your gender?
  • Woman
  • Man
  • Non-binary
  • Prefer to self-describe
  • Prefer not to say
Q21
Dropdown
In which region do you currently live?
  • North America
  • Europe
  • Latin America
  • Africa
  • Middle East
  • Asia
  • Oceania
  • Prefer not to say
Q22
Multiple Choice
What is the highest level of education you have completed?
  • Less than high school
  • High school or equivalent
  • Some college or associate degree
  • Bachelor's degree
  • Graduate or professional degree
  • Prefer not to say
Q23
Multiple Choice
Is English your primary language?
  • Yes
  • No
  • Prefer not to say
Q24
Multiple Choice
In the last 12 months, how often did you need help reading medical forms or documents?
  • Never
  • Rarely
  • Sometimes
  • Often
  • Always
  • Prefer not to say
Q25
Chat Message
Thank you for completing this survey. Your feedback will be used to improve the eConsent experience for future clinical trial participants. Your responses are confidential and will be reported only in aggregate.

Frequently Asked Questions

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