AI in Hypertension Treatment Education: Comparing GPT and Traditional Methods

NCT ID: NCT06776354

Last Updated: 2025-12-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

52 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-20

Study Completion Date

2025-07-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Medical Education Hypertension GPT

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

GPT-based training

Generative Pre-trained Transformer (GPT)-based training system

Group Type EXPERIMENTAL

GPT-based training

Intervention Type BEHAVIORAL

GPT-based training whether could improve the ability of students to develop effective hypertension management plans

traditional training

traditional training method

Group Type ACTIVE_COMPARATOR

traditional training

Intervention Type BEHAVIORAL

traditional teaching methods

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

GPT-based training

GPT-based training whether could improve the ability of students to develop effective hypertension management plans

Intervention Type BEHAVIORAL

traditional training

traditional teaching methods

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

zhen wang

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

zhen wang

physician-in-charge

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

xianrui luo

Role: STUDY_CHAIR

The Second Hospital of Anhui Medical University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

678 Furong Road, Economic Development Zone, Hefei City, Anhui Province, China

Hefei, Anhui, China

Site Status

Countries

Review the countries where the study has at least one active or historical site.

China

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2023jyxm1150

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

2023jyxm1150

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Smart-CKD/BP Study
NCT03501745 UNKNOWN NA
Standardized Antihypertensive Treatment Protocol
NCT06790927 NOT_YET_RECRUITING NA