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Pablo Rodriguez

Privacy Ethics

Respecting user data and privacy is part of good UX. Make privacy and ethics explicit across planning, recruitment, sessions, storage, and sharing.

  • Informed consent
    • Explain purpose, procedures, risks, benefits, and data handling.
    • Cover recording, storage, retention periods, access, and withdrawal rights.
  • Data minimization
    • Collect only what you need for the study. Avoid unnecessary PII.
    • Prefer IDs to names in notes; scrub identifying details in clips.
  • Secure handling
    • Store recordings and notes in approved, access‑controlled locations.
    • Define retention and deletion timelines; follow through and log deletions.
    • Limit access to a need‑to‑know audience; review access periodically.
  • Voluntary participation
    • Allow questions and breaks anytime; make it easy to stop without penalty.
  • Equity and inclusion
    • Recruit beyond convenience samples; include underrepresented users.
    • Budget time and resources for accommodations as a first‑class requirement.
  • Transparency
    • Be clear about prototype limitations and what is or isn’t functional.
    • Avoid overpromising or implying commitments beyond the study.
  • Personally identifiable information (PII)
    • Names, home addresses, email addresses, phone numbers.
  • Sensitive personally identifiable information (SPII)
    • SSNs, driver’s license/passport numbers, financial accounts, date of birth, race, disability status, gender, sexuality, criminal history, medical info.
    • Combine with PII increases risk; avoid collecting unless strictly necessary and approved.

Assistive Tech Readiness

  • Test your platform with screen readers, captions, and keyboard nav.
  • Provide transcripts and alt paths if visual content is essential.
  • Share setup instructions and support contacts before sessions.

Sharing Insights

  • Prefer anonymized clips and quotes; get re‑consent for broader sharing.
  • Limit raw data access; provide synthesized insights to stakeholders.
  • Track who has access; remove access when no longer needed.

Vulnerable Populations

  • Some groups have special privacy concerns or limited ability to consent (e.g., minors, elderly, incarcerated individuals, people with disabilities, LGBTQIA+).
  • Consult a research/ethics expert and follow applicable laws and guidelines.
  • De‑identification
    • Remove identifying info in notes and artifacts (use “Participant 1,” neutral pronouns, avoid unique descriptors).
  • Non‑disclosure agreements (NDA)
    • When testing unreleased ideas, NDAs protect your team’s intellectual property. Obtain signatures before sessions begin.

Summary: Treat privacy and ethics as design requirements. Minimize data, store it securely, be inclusive and transparent, and share findings responsibly to protect participants and maintain trust.