rct

Generate CONSORT-aligned reporting content for randomized controlled trials.

Updated Feb 23, 2026
One-click install
npx skills add https://github.com/olaTechie/scientific-paper-writer --skill rct
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: rct
Source: https://github.com/olaTechie/scientific-paper-writer/tree/main/skills/study-types/rct
Command: npx skills add https://github.com/olaTechie/scientific-paper-writer --skill rct

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes references (resource) components.

What problem does it solve?

RCT documentation and reporting consistency are enhanced by providing CONSORT-aligned templates, checklists, and guidance to draft transparent trial manuscripts.

Core Features & Use Cases

  • Structured templates for Methods, Results, and Discussion aligned to CONSORT 2010.
  • Guidance on trial design, eligibility criteria, randomisation, blinding, outcomes, and estimands.
  • References and mapping to the CONSORT checklist for audit-ready reporting.
  • Use case: a researcher drafts an RCT report with ensured compliance and reproducible methods.

Quick Start

Generate the CONSORT-aligned manuscript sections using the built-in templates provided.

Frequently Asked Questions about rct

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

FAQPage Schema
How do I write a CONSORT-aligned manuscript for a randomized controlled trial?

To write a CONSORT-aligned manuscript, use structured templates to generate Methods, Results, and Discussion sections. This ensures transparent reporting of trial design, randomisation, blinding, and outcomes for reproducible RCT documentation.

Can I generate CONSORT reporting for cluster and crossover trial designs?

Yes, you can generate CONSORT reporting for cluster and crossover trial designs. The templates support parallel, cluster, crossover, adaptive, and platform designs, providing specific guidance for each trial architecture.

What is the best way to define primary and secondary outcomes for clinical trial reporting?

The best way to define primary and secondary outcomes for clinical trial reporting is using structured templates that guide estimand definition and sample size rationale. This aligns your outcome reporting directly with CONSORT checklist requirements.

Does this RCT reporting template map to the CONSORT 2010 checklist?

Yes, the RCT reporting templates map directly to the CONSORT 2010 checklist. They provide integrated guideline references to ensure audit-ready compliance and complete reporting of randomisation and blinding details.

How do I document randomisation and blinding details for an RCT manuscript?

To document randomisation and blinding details for an RCT manuscript, use the built-in structured templates. They generate standardized sections that explicitly capture allocation methods and blinding protocols aligned with CONSORT guidelines.