clinical-research-tools

Name: clinical-research-tools
Availability: InStock
Author: DrugClaw

Guide clinical research protocol design, endpoint selection, and reporting guideline adherence.

126|8|Updated Mar 10, 2026

Search Tags:#protocol design #reporting guidelines #evidence synthesis #study design #clinical research #human subjects research

Ready to run

npx skills add https://github.com/DrugClaw/DrugClaw --skill clinical-research-tools

💬 Prompt for ChatGPT / Claude Chat▼

Please help me install this Agent Skill.
Skill: clinical-research-tools
Source: https://github.com/DrugClaw/DrugClaw/tree/main/skills/medical/clinical-research-tools
Command: npx skills add https://github.com/DrugClaw/DrugClaw --skill clinical-research-tools

SYSTEM DOCUMENTATION & REQUIREMENTS

What problem does it solve?

This Skill streamlines the complex process of designing, planning, and reporting human-subjects research, ensuring adherence to best practices and guidelines.

Core Features & Use Cases

Protocol Design: Assists in defining study designs, endpoints, and eligibility criteria.
Guideline Selection: Helps choose appropriate reporting guidelines (e.g., CONSORT, STROBE).
Evidence Synthesis: Guides the creation of clinical evidence summaries and reviews.
Use Case: A researcher needs to design a new clinical trial and is unsure about the best study design, primary endpoints, and reporting standards. This Skill provides a structured approach to define these elements and select the appropriate reporting guideline.

Quick Start

Use the clinical-research-tools skill to help design a protocol for a new randomized controlled trial.

Frequently Asked Questions about clinical-research-tools

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

FAQPage Schema

How do I design a clinical trial protocol with proper endpoints and eligibility criteria?▼

Clinical trial protocol design requires structured selection of study designs, primary endpoints, and eligibility criteria to ensure valid human-subjects research. This Skill provides a guided approach to define these protocol elements and establish appropriate statistical planning.

What reporting guidelines do I need for observational studies versus randomized controlled trials?▼

Reporting guidelines like CONSORT for randomized controlled trials and STROBE for observational studies ensure adherence to best practices in human-subjects research. This Skill helps you select the appropriate reporting guideline based on your specific study design.

Can I use this for clinical evidence synthesis and creating study reports?▼

Clinical evidence synthesis and study report creation are supported through guided generation of clinical evidence summaries, CSRs, and reviews. This Skill facilitates evidence grading and structured reporting to streamline the complex research reporting process.

What's the best way to plan statistical analysis for a new human-subjects research study?▼

Statistical planning for human-subjects research benefits from a structured protocol design approach that defines study designs and endpoints first. This Skill supports selecting appropriate statistical planning methods aligned with your chosen study design and reporting standards.

Does this help with evidence grading for clinical research summaries?▼

Evidence grading for clinical research summaries is a core feature that guides the creation of structured clinical evidence reviews. This Skill provides the necessary framework to evaluate and synthesize evidence according to established best practices.

When do I need to use specific reporting guidelines for clinical research?▼

Reporting guidelines are needed whenever you design and report human-subjects research to ensure adherence to best practices. This Skill helps you determine which guidelines apply based on your study type, whether it is a clinical trial or observational study.