RecruitingNCT06907927Updated Apr 2, 2025

Using Artificial Intelligence to Improve Radiologists' Performance in Radiology Report Writing: a Randomised Controlled Trial

An interventional study of Control group and Experimental group in Healthy, sponsored by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology. Recruiting at 1 site in China. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-04-02.

Sponsored by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Not applicable, Interventional, and Other

From the registry’s dates

Primary completion was expected by Apr 2025, 1 year 5 months ago, but the record still lists the study as recruiting.

Phase: Not applicable
Study type: Interventional
Enrollment: 100
Allocation: Randomized
Ages: 18 Years and older
Sex: All

Study summary

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.

Conditions studied

Healthy

In context

Lead sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology is the lead sponsor of 172 studies on the registry; 136 are open to participants now.

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Who can participate

Ages eligible: 18 Years and older
Sexes eligible: All
Accepts healthy volunteers: Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.）

Study design

Phase: Not applicable
Primary purpose: Other
Allocation: Randomized
Intervention model: Parallel assignment
Masking: Single (Outcomes assessor)
Enrollment: 100 participants (estimated)

Study arms

Placebo comparator
Control group
Behavioral: Control group
Experimental
Experimental group
Behavioral: Experimental group

Interventions

BehavioralControl 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
BehavioralExperimental 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

What researchers measure

Primary outcomes

Error rates in radiology reports
Statistical analysis of errors in radiology reports submitted by study and control group physicians
Time frame: 1 month

Study locations

1 of 1 sites recruiting

Union Hospital，Tongji Medical College，Huazhong University of Science and Technology
Wuhan, Hubei 430000, China
- Lian Yang · Contact · yanglian@hust.edu · 18986273791
Recruiting

Timeline

Tracking since Sep 25, 2026

ElapsedEstimatedEstimated, not yet reached

Start is estimated for Apr 2025; primary completion for Apr 2025, 0 months later.

How these figures are worked out, and which studies are left out of them.

Registered: Mar 26, 2025
First posted: Apr 2, 2025
StartEst.: Apr 1, 2025
Primary completionEst.: Apr 30, 2025
CompletionEst.: Apr 30, 2025
Last update: Apr 2, 2025

What these dates mean

Start.: When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.: When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.: When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.: Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.

No changes since tracking began. The registry record was last updated on Apr 2, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗

Registry details

Key details

Study ID: NCT06907927
Lead sponsor: Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Responsible party: Sponsor
First posted: Apr 2, 2025
Start date: Apr 1, 2025 (estimated)
Primary completion: Apr 30, 2025 (estimated)
Completion: Apr 30, 2025 (estimated)
Last update: Apr 2, 2025

Study contacts

Lian Yang

Contact

yanglian@hust.edu

18986273791

Oversight

FDA-regulated drug: No
FDA-regulated device: No

View the source record on ClinicalTrials.gov ↗

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