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.