Recruiting NCT06907927
Using Artificial Intelligence to Improve Radiologists' Performance in Radiology Report Writing: a Randomised Controlled Trial
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: Control group, Experimental group.
- Who it may be relevant to
- Registry conditions: Healthy. 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 →
Unsure about the terms? Read our patient guide →
Overview
This is a randomised controlled trial to assess whether artificial intelligence software can improve radiologists' performance in radiology report writing and improve the quality of radiology reports.
Interventions
- Behavioral Control group
the radiologists enrolled in the study will be randomly divided into two groups: the experimental group used AI(Artificial Intelligence) software to assist in the submission of radiology reports and the control group did not use any AI software to submit their reports - Behavioral Experimental group
the radiologists enrolled in the study will be randomly divided into two groups: the experimental group used AI(Artificial Intelligence) software to assist in the submission of radiology reports and the control group did not use any AI software to submit their reports
Primary outcome measures
- Error rates in radiology reports [Time frame: 1 month]
Eligibility criteria
Inclusion criteria
- Radiologists who submit reports;
- Clinical experience of less than 10 years and more than six months;
- An average of more than 10 radiology reports are submitted per day;
- Participants provided signed informed consent.
Exclusion criteria：
- Radiologists who review reports;
- Clinical experience of less than 6 months or more than 10 years;
- An average of less than 10 radiology reports are submitted per day.）
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
- Union Hospital，Tongji Medical College，Huazhong University of Science and Technology — Wuhan
Identifiers
NCT: NCT06907927 · 2025-0033