Menu
Not yet recruiting NCT06962423

AI-driven Automated Biomedical Research

No phase Interventional Biomedical Research Artificial Intelligence (AI)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: AI system.
Who it may be relevant to
Registry conditions: Biomedical Research, Artificial Intelligence (AI). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Study on Artificial Intelligence-based Automated Biomedical Research

Overview

This study will evaluate the effects of the AI system developed by our team on biomedical research.

Detailed description

It i a randomized-controlled study. Participants will be randomly assigned to the Intervention Group using our AI system and the Control Group. Both groups will perform the same biomedical research tasks and submit reports. At the end of the study, the research performance of the two groups will be evaluated.

Interventions

  • Other AI system
    Participants will complete the research task with the AI system developed by out team to perform automated biomedical research.

Primary outcome measures

  • Research quality evaluation scale [Time frame: Through study completion, an average of 1 week]
Secondary outcome measures (4)
  • Model performance [Time frame: Through study completion, an average of 1 week]
  • Research time cost [Time frame: Through study completion, an average of 1 week]
  • User evaluation [Time frame: Through study completion, an average of 1 week]
  • Model resource consumption [Time frame: Through study completion, an average of 1 week]

Eligibility criteria

Inclusion criteria

  • (1) Age ≥ 18 years old;
  • (2) Agree to sign consent form and invest time in this study;
  • (3) Able to understand and complete research tasks.

Exclusion criteria

  • (1) Currently participating in other projects that may interfere with this research and unable to ensure participation time;
  • (2) Have a history of major diseases or poor physical condition in the past three months that may affect research participation;
  • (3) Unwilling or unable to understand and complete the research tasks.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

China · 1 center
  • Tsinghua University — Beijing

Identifiers

NCT: NCT06962423 · THU01-20250025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗