Virtual Reality to Cope With Academic Stress

NCT ID: NCT05828329

Last Updated: 2024-07-11

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

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-04-02

Study Completion Date

2024-06-30

Brief Summary

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The new technologies may facilitate the teaching-learning process through the ubiquitous and active approach. However, stress from academic exams remains being high among undergraduate students. Although new technologies could be useful to simulate and control academic stressful situations through immersive virtual reality, no studies to date have evaluated its effectiveness. This study is designed to evaluate the effects of a virtual reality program to visualize stressful academic situations like exams on the level of psychological and physiological stress and academic performance of Physiotherapy and Nursing undergraduate students. To this end, an experimental study with two experimental groups and one control group is designed: experimental group 1 (EG1) will complete a 4-weeks program of guided visualization of exams through immersive virtual reality; experimental group 2 (EG2) will complete a 4-weeks program of traditional guided visualization of exams (through audio); control group (CG) will not receive any visualization program, as the most habitual strategy to cope with exams among students. Before and after the intervention period, all students will fulfill an online questionnaire to inform about their level of academic stress (SISCO inventory) and perceived stress from the last month (Perceived Stress Scale). Also, just before starting the exam they will have been visualizing, level of stress (0 to 10 points), blood pressure (mmHg), maximal heart rate (ppm) and salivary cortisol level will be assessed in all students. Qualifications of the exam will be also collected. Intra-group differences and between-group differences at post-intervention time will be obtained.

Detailed Description

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As eligibility criteria, participants should be enrolled in at least 80% of subjects of an usual academic course during the year in which the study is carrying out; and not to have previous experience in similar guided visualization to cope with stressful situations.

Intervention of EG1: The 4-weeks program with virtual reality will consist of a 30-minutes guided visualization session through virtual reality glasses (two sessions per week). Students will visualize a 360º video that simulates the entire experience of an exam, from first person perspective.

Intervention of EG2: The 4-weeks program of traditional visualization will consist of a 30-minutes traditional guided visualization session, by listening only the part of the audio used for EG1.

CG will not receive any intervention, as the most used strategy to cope with exams among students. After finishing the study, this group will receive the same program that EG1 or EG2 received, if they are interested.

The main outcomes will be the intra-group and between-group changes in the level of academic stress and the perceived stress from the last month. Also, between-group differences in the level of stress (0 to 10 points), arterial tension (mmHg), maximal heart rate (ppm) and salivary cortisol level just before exams.

As secondary outcomes, between-group differences in qualifications of exams that they will have been visualizing will be also considered (it will be taken into account their average qualifications in the degree).

Conditions

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Stress, Physiological Stress, Psychological

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized controlled trial
Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Investigators Outcome Assessors
Participants will be randomly assigned with a code with which investigators and outcomes assessors will not be able to know from whom data are or the group to which participants belong.

Study Groups

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Experimental group 1

The program with virtual reality will consist of a 30-minutes guided visualization session through virtual reality glasses. Students will visualize a 360º video that simulates the entire experience of an exam, from first person perspective.

Group Type EXPERIMENTAL

Guided visualization of exams through immersive virtual reality

Intervention Type BEHAVIORAL

During 4 weeks (twice per week), students will visualize a 30-minutes 360º video that simulates the experience of an exam, from first person perspective.

Experimental group 2

The 4-weeks program will consist of a 30-minutes traditional guided visualization session, by listening only the part of the audio used for EG1.

Group Type ACTIVE_COMPARATOR

Guided visualization of exams through traditional method

Intervention Type BEHAVIORAL

During 4 weeks (twice per week), students will listen a 30-minutes audio that explains the experience of an exam from first person.

Control group

This group will not receive any intervention, as the most used strategy to cope with exams among students.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Guided visualization of exams through immersive virtual reality

During 4 weeks (twice per week), students will visualize a 30-minutes 360º video that simulates the experience of an exam, from first person perspective.

Intervention Type BEHAVIORAL

Guided visualization of exams through traditional method

During 4 weeks (twice per week), students will listen a 30-minutes audio that explains the experience of an exam from first person.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* To be enrolled in at least 80% of subjects of an usual academic course during the year in which the study is carrying out.
* Not to have previous experience in guided visualization to cope with stressful situations.

Exclusion Criteria

* Not to understand the Spanish language
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of the Balearic Islands

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Natalia Romero-Franco, PhD

Role: PRINCIPAL_INVESTIGATOR

University of the Balearic Islands

Locations

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University of the Balearic Islands

Palma de Mallorca, Balearic Islands, Spain

Site Status

Countries

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Spain

References

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Seabrook E, Kelly R, Foley F, Theiler S, Thomas N, Wadley G, Nedeljkovic M. Understanding How Virtual Reality Can Support Mindfulness Practice: Mixed Methods Study. J Med Internet Res. 2020 Mar 18;22(3):e16106. doi: 10.2196/16106.

Reference Type RESULT
PMID: 32186519 (View on PubMed)

Riva G, Banos RM, Botella C, Mantovani F, Gaggioli A. Transforming Experience: The Potential of Augmented Reality and Virtual Reality for Enhancing Personal and Clinical Change. Front Psychiatry. 2016 Sep 30;7:164. doi: 10.3389/fpsyt.2016.00164. eCollection 2016.

Reference Type RESULT
PMID: 27746747 (View on PubMed)

Lacey C, Frampton C, Beaglehole B. oVRcome - Self-guided virtual reality for specific phobias: A randomised controlled trial. Aust N Z J Psychiatry. 2023 May;57(5):736-744. doi: 10.1177/00048674221110779. Epub 2022 Jul 11.

Reference Type RESULT
PMID: 35818296 (View on PubMed)

Other Identifiers

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IB4958/22PI

Identifier Type: -

Identifier Source: org_study_id

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