AI-driven Automated Biomedical Research

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorTsinghua University

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

(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.

Disqualifiers

(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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • AI system

    Other intervention

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

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Control groupNo intervention 0 interventions
Group B: Intervention groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Research quality evaluation scale

Independent senior experts will evaluate the research reports from the Intervention Group and the Control Group using a standardized 100-point Research Quality Evaluation Scale. A higher score indicates better research quality.

Time frame
Through study completion, an average of 1 week

Secondary outcomes

1

Model performance

The diagnostic accuracy, sensitivity, specificity, and area under the receiver-operating characteristic curve (AUC-ROC) will be reported to compare the performance of models generated by the Intervention Group and the Control Group.

Time frame
Through study completion, an average of 1 week
2

Research time cost

The time spent by the Intervention Group and the Control Group to complete tasks will be compared.

Time frame
Through study completion, an average of 1 week
3

User evaluation

User evaluation on the study will be assessed by Likert Scales.

Time frame
Through study completion, an average of 1 week
4

Model resource consumption

GPU usage rate and time and model size will be tracked and compared to evaluate the computational resource consumption of the Intervention Group and Control Group.

Time frame
Through study completion, an average of 1 week

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: