Write Protocol

Write-Protocol Skill

Draft the scientific core of an IRB/ethics protocol and leave institution-specific sections as [TODO] skeletons. Read both reference files before generating a protocol draft:

• ${CLAUDE_SKILL_DIR}/references/protocol_template.md -- the 10-section structure, per-section guidance, and the [TODO] blocks for Sections 5-9
• ${CLAUDE_SKILL_DIR}/references/ethics_checklist.md -- jurisdiction-specific ethical requirements

Inputs

Collect the required inputs before generating; ask for any that are missing.

• Required: research question / hypothesis (specific, testable); study type (retrospective cohort, prospective cohort, cross-sectional, RCT, diagnostic accuracy, case-control, case series); target population (who, where, when); primary outcome; secondary outcomes (if any).
• Optional: key references (DOIs or search terms); institution name (header and ethics guidance); regulatory context -- Korea (PIPA), US (HIPAA/Common Rule), EU (GDPR), other.

Use prior skill outputs directly when they exist; when they do not, ask the user or call the skill:

• design-study: design recommendations, analysis unit, comparator design, validation strategy.
• calc-sample-size: protocol/sample_size_justification.md (canonical IRB-ready prose) and protocol/sample_size_calc.{R,py} (reproducible code).
• search-lit: Background references with verified citations.
• define-variables: variable_operationalization.md -- literature-grounded definitions, cutoffs, DB-variable mappings for the Methods section. Precondition: if the study is observational and no operationalization artifact exists, call /define-variables before drafting Methods. Do not invent phenotype/cutoff definitions from the data dictionary inside this skill.

Protocol Structure -- 10 Sections

Core Sections (Fully Generated)

Section 1: Background and Rationale (400-600 words)

Full paragraphs, no bullet points, flowing from clinical context (disease burden, current practice) through the knowledge gap and rationale (what this study adds) to the research question or hypothesis. Call /search-lit if key references are not provided. Cite a reference only with a /search-lit-confirmed DOI or PMID; otherwise mark it [UNVERIFIED - NEEDS MANUAL CHECK].

Section 2: Study Design and Eligibility Criteria (300-500 words)

Prose covering the study design with its justification (why this design answers this question), the setting (single-center vs multi-center, institution description) and the study period, followed by numbered inclusion and numbered exclusion criteria. If design-study output is available, incorporate its analysis unit (patient vs lesion vs exam), comparator design, validation strategy, and leakage risks with mitigations. Mark any clinical definition, diagnostic criterion or guideline recommendation you cannot confirm [VERIFY] and ask the user.

Section 3: Sample Size Justification (150-300 words)

• If protocol/sample_size_justification.md exists (calc-sample-size output): embed it VERBATIM. Do not rephrase numbers.
• If not available: prompt the user to run /calc-sample-size first; only fall back to a basic justification if the user explicitly declines.
• Must include: test type, expected effect size (with literature source), alpha level, power, attrition adjustment.
• Final statement: "We plan to enroll N participants."

Section 4: Statistical Analysis Plan (300-500 words)

Full prose covering: descriptive statistics (continuous as mean (SD) or median (IQR); categorical as count (%)); the primary analysis (test, assumptions, handling of violations); pre-specified secondary analyses; pre-specified subgroup analyses with interaction tests; missing-data handling (complete case, multiple imputation, sensitivity analysis); software name and version (e.g., R 4.4.0, Python 3.12, SAS 9.4); two-sided alpha = 0.05 unless otherwise justified.

Skeleton Sections (TODO Markers)

Sections 5-9 are the [TODO] blocks from protocol_template.md, copied as they are; never fill them with invented institutional content.

• Section 5: Study Title and Registration
• Section 6: Data Collection and Management
• Section 7: Ethical Considerations -- also add the template's jurisdiction guidance for the regulatory context, and use ethics_checklist.md for the full checklist.
• Section 8: Timeline and Milestones
• Section 9: Budget

Section 10: References

A numbered list of the Section 1 citations, the Section 3 effect-size sources, and any references in the calc-sample-size output. Every entry has a verified DOI or PMID or is marked [UNVERIFIED - NEEDS MANUAL CHECK].

Output Format

Generate a single markdown file: protocol_draft.md

• All 10 sections with clear numbering (1. through 10.)
• Core sections (1-4) in full prose; the Section 2 eligibility criteria are the only lists
• Skeleton sections (5-9) with [TODO] markers clearly visible
• Word count targets noted in comments at the start of each core section
• Institution name in the header if provided

After generating, tell the user which sections are ready for review, which [TODO] items need their input, and the next steps (e.g., "Fill in Section 5 title and registration, then adapt Section 7 to your IRB form").

Quality Checks

Before delivering the protocol:

1. Citation integrity: every reference has a DOI or PMID, or is marked [UNVERIFIED - NEEDS MANUAL CHECK]
2. Internal consistency: sample size in Section 3 matches the analysis plan in Section 4
3. Design alignment: study type in Section 2 matches the statistical approach in Section 4
4. TODO completeness: all institution-specific items have [TODO] markers
5. Word counts: core sections fall within target ranges
6. No AI patterns: avoid phrases like "it is worth noting", "comprehensive", "plays a crucial role"