Help define what Parkinson app data is clinically useful, safe, and not just noise.

This form asks clinicians about consultation friction, pre-visit summaries, red flags, app/game acceptability, and evidence or workflow requirements before recommending any tool.

Start MD questionnaire

Privacy note: Do not include clinician names, employer names, patient names, dates of birth, exact medication schedules, institutions, or identifiable patient stories.

Medical safety note: This site is for education and evidence translation. It does not replace a clinician, diagnosis, treatment plan, medication advice, or emergency care.

Storage

With consent, responses are stored in protected Cloudflare D1 storage for MJJ product discovery. Optional email is stored separately only if follow-up is selected.

Parkinson clinician / MD questionnaire

Workflow, safety, and clinical acceptability.

This is professional product discovery and research planning, not individual clinical decision support.

Evidence, safety, adoption, and follow-up What would need to be true before you would recommend or review output from this tool? What should an ideal one-page appointment summary contain? Advice for a small pilot

May we contact you for follow-up questions or prototype testing?

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Email address only if you want follow-up

Before submitting

This is product discovery and research planning, not clinical decision support.
Do not include identifiable patient cases, institutions, clinician names, or exact medication schedules.
Your response will be stored for MJJ discovery if you submit with consent.

I understand this is product discovery, not medical advice or clinical decision support, and I will not include identifiable patient/professional details. I consent to MJJ storing my clinician / MD questionnaire response for product discovery and research planning.

You can request deletion later using the reference ID returned after submission.