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Clinical Trials/NCT06839573
NCT06839573Not yet recruitingNot Applicable

Effectiveness of Immersive Virtual Reality to Improve Learning Outcomes in Nursing Degree Students: A Randomized Clinical Trial

Universitat Jaume I0 sites140 target enrollmentStarted: March 5, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
140
Primary Endpoint
Compare the satisfaction

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Triple (Participant, Care Provider, Investigator)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Arms & Interventions

NON RV CONTROL

No Intervention

Group Control

RV INTERVENTION

Experimental

Experience with virtual reality glasses

Intervention: Experience with virtual reality glasses (Other)

Outcomes

Primary Outcomes

Compare the satisfaction

Time Frame: Five months

To compare the satisfaction acquired by students when performing basic cardiopulmonary resuscitation and patient examination between both teaching groups (experimental group - EG: VR plus in-person simulation, control group - CG: in-person simulation). We will mesure this with Satisfaction and Self-Confidence in Learning Scale (SCLS-Sp) (Farrés-Tarafa et al., 2021) .

Compare the self-confidence

Time Frame: Five months

To compare the self-confidence acquired by students when performing basic cardiopulmonary resuscitation and patient examination between both teaching groups (experimental group - EG: VR plus in-person simulation, control group - CG: in-person simulation). We will mesure this with Satisfaction and Self-Confidence in Learning Scale (SCLS-Sp) (Farrés-Tarafa et al., 2021) .

Secondary Outcomes

  • To compare the acquisition of knowledge in each teaching group.(Five months)
  • To compare the acquisition of skills in each teaching group.(Five months)
  • To evaluate students' tolerance to VR headset technology.(Five months)
  • To assess the usability of VR headsets by students.(Five months)
  • To analyze the costs of traditional teaching with in-person simulation compared to teaching with VR.(Five months)

Investigators

Sponsor
Universitat Jaume I
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Isabel Almodóvar Fernández

Principal Investigator

Universitat Jaume I

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