AI in Hypertension Treatment Education: Comparing GPT and Traditional Methods (AIHT-EDU)

zhen wang

Status

Completed

Conditions

Hypertension

Medical Education

GPT

Treatments

Behavioral: GPT-based training

Behavioral: traditional training

Study type

Interventional

Funder types

Other

Identifiers

NCT06776354

2023jyxm1150 (Other Grant/Funding Number)

Details and patient eligibility

About

Educational Trial: GPT-Based Training vs. Traditional Teaching for Hypertension Management

The goal of this educational trial is to determine whether a Generative Pre-trained Transformer (GPT)-based training system is more effective than traditional teaching methods in helping medical students master hypertension management plans. It will also evaluate the educational effectiveness and engagement of the GPT-based system. The main questions it aims to answer are:

Does the GPT-based training improve the ability of students to develop effective hypertension management plans compared to traditional methods? How do students perceive the use of the GPT system in their learning process? Researchers will compare the GPT-based training system to traditional teaching methods to see if the innovative AI approach enhances learning outcomes in medical education.

Participants will:

Engage with either the GPT-based system or traditional teaching materials. Visit the educational facility periodically for assessments and feedback sessions.

Keep a diary of their learning experiences, noting any difficulties or advantages they observe in the training method they are assigned.

Enrollment

52 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Graduate or regulatory trainee, currently rotating in cardiology and willing to participate in research.
Age between 18-30 years old, gender not limited.
No specialized training experience in hypertension diagnosis and treatment, only possessing basic medical theoretical knowledge.
Able to accept a 4-week teaching intervention (2 hours of study per week).
Sign the informed consent form and be aware of the research purpose and process.

Exclusion criteria

Graduate students or trained interns who have received specialized training in hypertension medication treatment.
Students unable to complete the full course of study (e.g., rotations shorter than four weeks or potential mid-course withdrawal).
Unable to consistently participate in educational interventions (e.g., conflicts with study schedule).
Have severe physical or mental health issues that may affect the learning process.
Have language comprehension barriers or cognitive impairments, making it difficult to complete learning tasks.