NCT06706011

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
56

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 26, 2024

Completed
14 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 9, 2024

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 10, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

October 28, 2024

Completed
29 days until next milestone

First Posted

Study publicly available on registry

November 26, 2024

Completed
Last Updated

November 26, 2024

Status Verified

November 1, 2024

Enrollment Period

14 days

First QC Date

October 28, 2024

Last Update Submit

November 25, 2024

Conditions

Keywords

virtual patienteducation

Outcome Measures

Primary Outcomes (4)

  • General Self-Efficacy Scale

    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

    Measuring self-efficacy. Scale 1-10: 1=Low, 10=High.

    Up to two months

  • Level of Knowledge - Test

    Measuring level of knowledge. 15 multiple-choice question about inpartner violence.

    Up to two months

  • Level of Knowledge - Visual Analog Scale

    Measuring level of knowledge, Scale 1-10: 1=Low, 10=High.

    Up to two months

Study Arms (2)

Intervention

EXPERIMENTAL

Virtuel Patient

Other: Virtual Patient

Control

NO INTERVENTION

No Virtuel Patient

Interventions

Interactive Educational Activity

Intervention

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \* Students in Nursing Program

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre for Psychatry Research, Karolinska Institutet

Stockholm, Sweden

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

October 28, 2024

First Posted

November 26, 2024

Study Start

August 26, 2024

Primary Completion

September 9, 2024

Study Completion

September 10, 2024

Last Updated

November 26, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

Locations