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Development and Validation of a Training System for Management of Women with Abnormal Cervical Cancer Screening Results Based on AI Virtual Patients and Intelligent Coaching

Development and Validation of a Training System for Management of Women with Abnormal Cervical Cancer Screening Results Based on AI Virtual Patients and Intelligent Coaching

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115267
Enrollment
Unknown
Registered
2025-12-24
Start date
2025-12-28
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Cervical cancer

Interventions

Physician Intervention Group:AI-SP/coach training
Physician Control Group:Traditional training
Patient Intervention Group:Patients are seen by physicians in the intervention group.
Patient Control Group:Patients are seen by physicians in the control group.

Sponsors

Chinese Academy of Medical Sciences and Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Physicians: 1. Responsible for clinical tasks related to the interpretation of abnormal cervical cancer screening results, clinical decision-making, and follow-up management. 2. Capable of using computers and the Internet for online learning. 3. Provide informed consent and voluntarily participate in this study. Patients: 1. Female patients aged >=18 years; 2. Attend outpatient consultations with participating physicians regarding cervical cancer screening-related issues (e.g., receiving an abnormal result, seeking guidance on subsequent management); 3. Possess normal comprehension and communication abilities; 4. Understand the study and voluntarily provide written or verbal informed consent.

Exclusion criteria

Exclusion criteria: Physicians: 1. Primarily engaged in administrative or teaching work rather than clinical practice; 2. Previously involved in any development or testing of the training system; 3. Hold senior professional titles with extensive clinical experience (thus not representing the target trainee group); 4. Unable to complete online training due to practical constraints (e.g., lack of stable Internet access). Patients: 1. Individuals with severe cognitive impairment or mental disorders that impede effective communication; 2. Those currently in an emergency medical condition; 3. Individuals with language or hearing impairments without access to an appropriate interpreter.

Design outcomes

Primary

MeasureTime frame
Quality of Management Decisions;Communication Skills;

Secondary

MeasureTime frame
System Usability;Patient Psychological Outcomes;Patient Adherence;Patient Satisfaction with Care;

Countries

China

Contacts

Public ContactMingyang Chen

Chinese Academy of Medical Sciences and Peking Union Medical College

chenmy265@163.com+86 159 8900 2908

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026