preregistration

Automates preregistration of study protocols and analysis plans to multiple platforms.

6|2|Updated Jun 11, 2026
One-click install
npx skills add https://github.com/pradyumnasagar/open-research-skills --skill preregistration
Or copy as Structured Prompt for Agent
Please help me install this Agent Skill.
Skill: preregistration
Source: https://github.com/pradyumnasagar/open-research-skills/tree/main/skills/open-science/preregistration
Command: npx skills add https://github.com/pradyumnasagar/open-research-skills --skill preregistration

SYSTEM DOCUMENTATION & REQUIREMENTS

💡 This Skill includes scripts (resource) and references (resource) components.

What problem does it solve?

This Skill streamlines the process of preregistering research studies, ensuring compliance and facilitating transparency.

Core Features & Use Cases

  • Preregistration: Automates the preregistration of study designs, analysis plans, and outcomes.
  • Platform Support: Integrates with OSF Registries, AsPredicted, ClinicalTrials.gov, and Registered Report formats.
  • Use Case: When you need to preregister a clinical trial or study protocol to ensure transparency and replicability.

Quick Start

Run the 'preregister' command to initiate the preregistration process for your study.

Frequently Asked Questions about preregistration

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

FAQPage Schema
How do I automate study preregistration for clinical trials and research protocols?

You can automate study preregistration by running the 'preregister' command, which requires a study protocol and relevant platform account to initiate the process for your research design.

Does this support OSF Registries, AsPredicted, and ClinicalTrials.gov formats?

Yes, preregistration supports multiple platforms including OSF Registries, AsPredicted, ClinicalTrials.gov, and Registered Report formats to ensure compliance and facilitate transparency.

What do I need to specify when preregistering a study design for transparency?

To preregister a study design for transparency, you need to provide a study protocol, specify your analysis plan, and define the expected outcomes to ensure full replicability.

When should I use an automated preregistration tool for research studies?

You should use automated preregistration when you need to preregister a clinical trial or study protocol to ensure research ethics, transparency, and replicability before data collection begins.

Can I use this skill to document my analysis plan and outcome specification?

Yes, the skill automates the documentation of your analysis plan and outcome specification, streamlining the process to ensure your study design is fully compliant and transparent.