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write-protocol

Convert study inputs into structured IRB protocol documents with core and skeleton sections.

243|60|Updated Apr 6, 2026
Search Tags:#templates#protocol#ethics#IRB#research-design#sample-size#cross-skill
One-click install
npx skills add https://github.com/Aperivue/medsci-skills --skill write-protocol
Or copy as Structured Prompt for Agent▼
Please help me install this Agent Skill.
Skill: write-protocol
Source: https://github.com/Aperivue/medsci-skills/tree/main/skills/write-protocol
Command: npx skills add https://github.com/Aperivue/medsci-skills --skill write-protocol

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes references (resource) components.

What problem does it solve?

Drafting IRB/ethics submission documents is time-consuming and error-prone when translating study ideas into formal submission content. This skill automates the creation of a structured protocol by synthesizing inputs from related skills (design-study, calc-sample-size, and search-lit) and by applying approved templates from the referenced materials.

Core Features & Use Cases

  • Generates 4 core sections with full prose: Background and Rationale; Study Design and Eligibility Criteria; Sample Size Justification; Statistical Analysis Plan.
  • Provides 6 skeleton sections with [TODO] markers to accommodate institution-specific content.
  • Integrates outputs from design-study, calc-sample-size, and search-lit to ensure consistency and traceability.
  • Outputs can be adapted for different regulatory environments using the included ethics_checklist and protocol templates in references.

Quick Start

Provide the required inputs and let the skill generate a complete protocol draft using the templates and cross-skill outputs.

Frequently Asked Questions about write-protocol

High-intent search queries and answers about installing and using this skill.

FAQPage Schema
How do I draft an IRB protocol from my study design inputs?▼

Auto-generate an IRB protocol by synthesizing study design, sample size, and literature review inputs into a structured document with full prose core sections and marked skeleton sections for institutional review.

What sections are included in an auto-generated ethics submission protocol?▼

An auto-generated ethics submission protocol includes four fully drafted core sections—Background, Study Design, Sample Size Justification, and Statistical Analysis Plan—plus six skeleton sections marked with TODOs for custom institutional content.

Does this protocol generation tool work with both prospective and retrospective studies?▼

Yes, this protocol generation tool works for both prospective and retrospective studies requiring a full protocol, ensuring alignment with available templates and preparing artifacts for institutional review.

Can I integrate sample size calculations and literature search results into my IRB submission?▼

Yes, you can integrate sample size calculations and literature search results into your IRB submission. The tool synthesizes outputs from design-study, calc-sample-size, and search-lit to ensure protocol consistency and traceability.

What's the best way to prepare an ethics checklist for regulatory review?▼

The best way to prepare an ethics checklist for regulatory review is to apply the included ethics_checklist and protocol templates to adapt your generated protocol draft for different regulatory environments.

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