Effectiveness of Immersive Virtual Reality in Nursing Students' Learning

NCT ID: NCT06839573

Last Updated: 2025-02-21

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

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

140 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-05

Study Completion Date

2025-05-08

Brief Summary

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Teaching using VR for basic cardiopulmonary resuscitation and patient examination (experimental group) will not result in differences in knowledge and skill acquisition compared to traditional classroom-based simulation teaching (control group), but it will lead to greater satisfaction and self-confidence. Open, single-center randomized clinical trial involving fourth-year nursing degree students at a public university. Participants will be assigned based on their usual teaching groups (ratio of 6-8 students per instructor) and, according to randomization, will receive a 1:1 assignment to either the control group (classroom-based simulation teaching) or the experimental group (classroom-based simulation teaching combined with VR headset teaching). The CONSORT checklist will be followed to report the study.

Detailed Description

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Conditions

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Informed Consent

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Open, single-center randomized clinical trial involving fourth-year nursing degree students at a public university. Participants will be assigned based on their usual teaching groups (ratio of 6-8 students per instructor) and, according to randomization, will receive a 1:1 assignment to either the control group (classroom-based simulation teaching) or the experimental group (classroom-based simulation teaching combined with VR headset teaching). The CONSORT checklist will be followed to report the study.
Primary Study Purpose

OTHER

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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RV INTERVENTION

Experience with virtual reality glasses

Group Type EXPERIMENTAL

Experience with virtual reality glasses

Intervention Type OTHER

If the group belongs to GE (teaching with in-person simulation in the classroom and teaching with VR headsets), they will also receive the two training sessions described for GC:

30 minutes of individual training through VR (headsets and controllers to perform actions while receiving immediate feedback through VR) before the in-person simulation.

NON RV CONTROL

Group Control

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Experience with virtual reality glasses

If the group belongs to GE (teaching with in-person simulation in the classroom and teaching with VR headsets), they will also receive the two training sessions described for GC:

30 minutes of individual training through VR (headsets and controllers to perform actions while receiving immediate feedback through VR) before the in-person simulation.

Intervention Type OTHER

Other Intervention Names

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Formative intervention

Eligibility Criteria

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Inclusion Criteria

\- having completed the scheduled in-person simulation in previous years of the degree .

Exclusion Criteria

-the student does not sign the informed consent to participate in the study.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Barcelona

OTHER

Sponsor Role collaborator

Universidad Complutense de Madrid

OTHER

Sponsor Role collaborator

Universitat Jaume I

OTHER

Sponsor Role lead

Responsible Party

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Isabel Almodóvar Fernández

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Isabel Almodóvar-Fernández, PhD

Role: CONTACT

+0034636760923

Marta Raurell-Torredà, phD

Role: CONTACT

Other Identifiers

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UB-UJI-RV25

Identifier Type: -

Identifier Source: org_study_id

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