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Phase Not Applicable
All Genders
Healthy Volunteers
ID06699433

Utilizing Artificial Intelligence-driven Virtual Standardized Pediatric Patients to Enhance Primary Healthcare Doctors' Capabilities for Managing Common Pediatric Diseases in China: A Randomized Controlled Trial

Led by Southern Medical University, China · Updated on 2024-12-19

459

Participants Needed

3

Research Sites

4 weeks

Total Duration

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AI-Summary

What this Trial Is About

Researchers are evaluating the use of artificial intelligence-driven virtual standardized patients (VSPs) to improve the ability of primary care doctors in China to manage common pediatric diseases. The study addresses challenges in China's pediatric healthcare system, including limited capacity in primary care and a lack of effective training tools. It involves a randomized controlled trial with over 459 doctors from various specialties across more than 10 provinces, aiming to enhance pediatric care through innovative training methods. The trial involves three groups: one using a virtual patient platform where doctors interact with AI-driven simulated patients covering diseases like pneumococcal pneumonia, rotavirus enteritis with hypovolemic shock, hand-foot-and-mouth disease, acute appendicitis, and respiratory failure; another group uses case teaching manuals, and the third group uses case teaching videos. Participants engage in a two-week learning period with their assigned training method. During the study, doctors' management skills will be assessed through clinical vignettes to measure adherence to best clinical practice guidelines. Researchers will monitor diagnosis accuracy, examination scores relevant to disease handling, and doctors' focus on patient needs. The study runs for about six months and includes over 300 primary healthcare institutions to ensure wide representation. The trial also evaluates the acceptance and costs of the training methods used.

CONDITIONS

Brief Title

Artificial Intelligence-driven Virtual Standardized Pediatric Patients Trial

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Medical institutions including primary and secondary hospitals
  • Community health centers, township health centers, village health clinics, and clinics
  • Practicing (assistant) doctors and rural doctors working at eligible institutions
  • Doctors specialized in general practice, internal medicine, surgery, or pediatrics
Not Eligible

You will not qualify if you...

  • Specialized medical institutions such as specialized hospitals and dental clinics
  • Public health prevention and treatment institutions like tuberculosis prevention centers
  • Ethnic medicine institutions such as Mongolian and Tibetan hospitals
  • Hospitals above the secondary level
  • Hospitals not yet graded due to short establishment or unstable operations

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or virtual)

Outpatient Treatment

Duration - Approximately 6 months

Participants receive behavioral training interventions including interacting with virtual standardized patients, using case teaching manuals, or case teaching videos to enhance their capabilities for managing common pediatric diseases.

Training sessions as scheduled over the study period

Trial Site Locations

Total: 3 locations

1

Yuntan Street Community Health Center

Guiyang, Guizhou, China, 550081

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2

Jinxi County People's Hospital

Fuzhou, Jiangxi, China, 344899

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3

Honghe County People's Hospital

Yisa, Yunnan, China, 654499

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Research Team

L

Luo

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

3

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