🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Spain / NCT06809634
Recruiting Phase 2

Large Linguistic Model for Clinical Reaoning of Physical Therapy Students

NCT06809634 · tracked via the Priya Life Science Spain tracker
Phase
Phase 2
Started
2023-09-01
Last updated
2025-12-04

Condition(s) studied

HealthyArtificial Intelligence (AI)

Investigational drug(s) / intervention(s)

Large Language ModelConventional

Large Language Model: The intervention in the experimental group is distinguished by the integration of a Large Language Model (LLM)-based interactive platform (ChatGPT) into clinical reasoning training for physical therapy students. Unlike traditional educational approaches, this intervention provides real-time, AI-generated patient interactions, allowing students to actively engage in virtual clinical case simulations.

Conventional: The intervention in the control group follows a traditional case-based learning approach, which is commonly used in physical therapy education. Unlike the experimental group, this training method relies solely on human-led instruction and written case analysis, without the integration of artificial intelligence or interactive digital tools.

Study summary

Clinical reasoning is a fundamental skill for physical therapy students, enabling them to collect and interpret patient information to make accurate diagnoses and treatment decisions. Traditional training methods often limit students' exposure to a diverse range of clinical cases, which can restrict the development of these skills. The integration of Large Language Models (LLMs), such as ChatGPT, into physical therapy education offers a novel approach to enhance clinical reasoning by simulating interactive and realistic patient scenarios.

This randomized controlled trial aims to evaluate the effectiveness of an LLM-based educational intervention in improving clinical reasoning skills in physical therapy students. The study will recruit a total of 200 third-year physiotherapy students from multiple university institutions. Participants will be randomly assigned to one of two groups:

1. Experimental Group - Students will receive LLM-based training, engaging with a conversational artificial intelligence model to solve clinical cases over an 8-week period. The model will provide real-time responses to their questions, allowing them to refine their diagnostic and treatment reasoning.
2. Control Group - Students will follow the standard curriculum, participating in conventional case-based learning and supervised clinical reasoning exercises without AI-based assistance.

The primary outcome of the study is the improvement in clinical reasoning skills, assessed through standardized written case evaluations and structured practical examinations. Secondary outcomes include changes in digital competence, student engagement levels, overall satisfaction with the educational approach, and cost-effectiveness of the intervention.

By assessing the impact of LLMs on clinical reasoning training, this study seeks to determine whether AI-driven educational tools can effectively complement traditional physiotherapy education and improve student preparedness for real-world clinical practice.

Eligibility

Sex
ALL
Min age
18 Years
Max age
30 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Students enrolled in the third year of the Physiotherapy program at La Salle Centre for Higher University Studies (LCHUS) * Participants must be between 18 and 30 years old. * Students must agree to participate in the study by signing an informed consent form after being briefed about the study's objectives, procedures, and potential risks. * Participants must be willing to engage with the LLM-based platform (for the experimental group) or participate in traditional learning activities (for the control group) for the duration of the study. Exclusion Criteria: * Students with previous clinical experience beyond the third year of physiotherapy education. * Physical or cognitive disabilities that may interfere with the ability to participate in or benefit from the intervention (e.g., vision, hearing, or motor impairments). * Students who do not provide informed consent to participate in the study. * Students who do not possess sufficient proficiency in Spanish or English to understand the materials and the intervention.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centro Superior de Estudios Universitarios La Salle Madrid Madrid Recruiting

More Neuron, Spain trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06809634 on ClinicalTrials.gov ↗ ← All trials in Spain