# Default Intake & Protocol Design Prompt

Copy, complete, and send the following to initiate a high-quality protocol design session:

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Act as Vesper, the Microdosing Protocol Architect. Design a rigorous, safety-first, personalized microdosing protocol for me as a proper n-of-1 experiment.

**Demographics & Context**
- Age, gender/sex (relevant for biology):
- Country/region (legal context only):
- Occupation and general life structure:

**Primary Goals** (be specific and, where possible, measurable):
1.
2.
3.

**Substance Preference & Access**
- Preferred substance (psilocybin mushrooms / LSD / other):
- Form and estimated potency (if known):
- Prior experience (macro or micro doses and dates):

**Mandatory Health & Safety Disclosure** (incomplete answers will delay or prevent protocol design)
- Current medications (including dose and duration):
- Current supplements:
- Diagnosed mental or physical health conditions (past and present):
- Family mental health history (psychosis, bipolar, suicide, schizophrenia):
- Cardiovascular health summary:
- Pregnancy / breastfeeding / trying to conceive status:
- Age considerations or any other relevant medical notes:

**Lifestyle & Practical Constraints**
- Typical weekly schedule and high-stakes days I cannot dose:
- Current sleep, exercise, diet, and stress patterns:
- Do you have (or can you obtain) a 0.001 g precision scale?
- Support system (therapist, partner, trusted friend aware of this plan):

**Motivation & History**
- Why are you considering microdosing at this specific time?
- What have you already tried for these goals?
- Any specific concerns, fears, or past difficult experiences with psychedelics?

Please:
1. Acknowledge the information and ask any critical additional screening or clarifying questions.
2. Summarize your understanding of my goals and reframe them into measurable terms.
3. Present 2 protocol options with clear trade-offs.
4. Provide a detailed recommended protocol including exact dose ranges, calendar, titration rules, and preparation instructions.
5. Supply a ready-to-use daily tracking template with specific metrics and recommended tools.
6. Detail integration practices, red flags, exit criteria, and scheduled review points.
7. Include all necessary legal, medical, and safety disclaimers.

Begin now.

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This prompt elicits the information required for a truly personalized, responsible, and high-quality protocol design.