Virtual Patients - An Interactive Educational Module for Higher Education

November 25, 2024 updated by: Karolina Sörman, Karolinska Institutet

Swedish Title: Virtuella Patienter - en Interaktiv Utbildningsmodul Inom Universitet Och högskola. In English: Virtual Patients - An Interactive Educational Module in Universities and Colleges.

Popular Science Summary (for the whole project)

In modern healthcare, several challenges exist: short patient visits, highly specialized care, and limited opportunities for education and professional development among healthcare staff. In theoretical training efforts, it can be difficult to highlight and provide opportunities to practice complex patient interactions. The overall goal of this project is to evaluate the effects of an interactive educational module that includes training with virtual patients (VP). Single training sessions rarely lead to behavioral changes in clinical practice, but concrete training with a clear connection to clinical tasks can have a better effect.

In this research project, VPs will be part of an educational module at universities and colleges, where the overarching goal is for students to practice clinically relevant communication areas. Two main areas have been selected for the VP in this project: intimate partner violence and suicide risk assessment. Both of these areas are of great significance to public health and have direct relevance to clinical care, especially in psychiatry. Specific objectives of the project include exploring the user experience of the VP, examining whether the VP contributes to increased knowledge and confidence in asking questions within the chosen focus area, studying students' experiences of using the VP, how it has influenced their work with patients after graduation, and finally, examining user patterns on the VP platform.

Previous research suggests that virtual patient cases can have positive effects on learning and engagement and may even be more effective than traditional education in improving clinical decision-making and critical thinking skills. VPs have been studied in various medical specialties, but there is a lack of knowledge specifically in psychiatry. In this project, researchers will evaluate the use of VPs in psychiatric training within medical, nursing, and psychology programs.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Overall purpose (for the whole project):

To investigate virtual patient cases (VP) as an interactive educational module for students in universities and colleges. The educational module will consist of three parts: a theoretical and preparatory lecture, training with VP, and a follow-up seminar. The aim is to evaluate how well this module prepares students to ask clinically relevant questions in focus areas such as intimate partner violence and suicide risk assessment. The target group for the project is students in nursing, medical, and psychology programs at various universities and colleges in Sweden.

Specific aims for this study:

To investigate whether VP contributes to an increased level of knowledge and confidence in asking questions within the selected focus areas among students in nursing, medical, and psychology programs.

Focus areas for VP:

Intimate partner violence

Study Type

Interventional

Enrollment (Actual)

56

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Stockholm, Sweden
        • Centre for Psychatry Research, Karolinska Institutet

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

* Students in Nursing Program

Exclusion Criteria:

* None, except if the student does not want to participate

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
Virtuel Patient
Interactive Educational Activity
No Intervention: Control
No Virtuel Patient

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
General Self-Efficacy Scale
Time Frame: Up to two months
This scale is a self-report measure of self-efficacy. Likert scale 1-4: 1=Not at all true, 2=Hardly true, 3=Moderately true, 4=Exactly true.
Up to two months
General Self-Efficacy - Visual Analog Scale
Time Frame: Up to two months
Measuring self-efficacy. Scale 1-10: 1=Low, 10=High.
Up to two months
Level of Knowledge - Test
Time Frame: Up to two months
Measuring level of knowledge. 15 multiple-choice question about inpartner violence.
Up to two months
Level of Knowledge - Visual Analog Scale
Time Frame: Up to two months
Measuring level of knowledge, Scale 1-10: 1=Low, 10=High.
Up to two months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 26, 2024

Primary Completion (Actual)

September 9, 2024

Study Completion (Actual)

September 10, 2024

Study Registration Dates

First Submitted

October 28, 2024

First Submitted That Met QC Criteria

November 25, 2024

First Posted (Estimated)

November 26, 2024

Study Record Updates

Last Update Posted (Estimated)

November 26, 2024

Last Update Submitted That Met QC Criteria

November 25, 2024

Last Verified

November 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 2023-06687-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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