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AI-agent enhanced training for chest-port insertion in interventional radiology trainees

Faculty-supervised artificial intelligence-agent enhanced competency-based training for chest-port insertion: an assessor-blinded three-arm randomized controlled educational trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260710008
Enrollment
90
Registered
2026-07-10
Start date
2026-07-07
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Interventional radiology procedural competency Chest-port insertion training Vascular access procedural education Artificial Intelligence Clinical Competence Education Medical Graduate Simulation Training Radiology Interventional Vascular Access Devices Central Venous Catheterization Chest Port Direct Observation of Procedural Skills Objective Structured Assessment of Technical Skills

Interventions

Participants will receive standard faculty-led chest-port insertion training, including didactic teaching, procedural videos, SIC-Port and RaCeVA checklist rehearsal, model-based demonstration, case d
Intervention Name: Conventional faculty-led training,AI-agent self-learning ,Faculty-supervised AI-agent training

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Interventional radiology residents, fellows, specialty trainees, visiting trainees, or junior physicians participating in structured vascular access training. 2. Currently receiving training related to chest-port insertion or ultrasound-guided central venous access. 3. Prior independent chest-port insertion experience of fewer than 30 cases. 4. Able to complete baseline assessment, assigned training activities, and post-training assessment. 5. Able and willing to provide informed consent for participation and anonymized educational data analysis.

Exclusion criteria

Exclusion criteria: 1. Prior independent chest-port insertion experience of 30 cases or more. 2. Prior participation in the development, testing, or validation of the IR-Port-Agent training system. 3. Inability to complete either baseline or post-training assessment. 4. Failure to complete the minimum assigned training dose. 5. Refusal to allow anonymized educational performance data to be used for research. 6. Concurrent participation in another structured chest-port insertion training intervention during the study period.

Design outcomes

Primary

MeasureTime frame
DOPS score change Baseline and within 14 days after completion of the assigned training Change in Direct Observation of Procedural Skills score from baseline to post-training assessment.

Secondary

MeasureTime frame
OSATS score change Baseline and within 14 days after training completion Change in Objective Structured Assessment of Technical Skills score from baseline to post-training assessment, rated by blinded expert assessors using a structured procedural skill rubric.,SIC-Port checklist adherence Post-training assessment within 14 days after training completion Percentage of required SIC-Port procedural checklist items correctly completed during simulated chest-port insertion assessment.

Countries

China

Contacts

Public ContactZeyang Fan

Peking Univeristy First Hospital

fanzeyang555@163.com15116920302

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026