- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05828329
Virtual Reality to Cope With Academic Stress
Virtual Reality to Cope With Academic Exams: Effects on Stress and Academic Performance in Physiotherapy and Nursing Students of University of the Balearic Islands
Study Overview
Status
Conditions
Detailed Description
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).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Balearic Islands
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Palma De Mallorca, Balearic Islands, Spain, 07122
- University of the Balearic Islands
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 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.
|
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.
|
|
Active Comparator: 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.
|
During 4 weeks (twice per week), students will listen a 30-minutes audio that explains the experience of an exam from first person.
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|
No Intervention: Control group
This group will not receive any intervention, as the most used strategy to cope with exams among students.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Academic stress
Time Frame: 4 weeks
|
Between-group and intra-group differences in academic stress, which will be registered with the SISCO Inventory version-21.
This is the 21-items "Inventario SIStémico COgnoscitivista" for the study of the academic stress, composed by 21 items: the first item is dichotomous (yes-no) and the remaining 20 items are 5-point Likert scale, scored from 1 (never) to 5 (always).
The maximal punctuation is 100 (maximal stress).
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4 weeks
|
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Perceived stress in the last month
Time Frame: 4 weeks
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Between-group and intra-group differences in perceived stress of the last month, which will be registered with the Perceived Stress Scale.
This survey has 10 questions (using Likert scales from 0-5, being 0 never and 5 very often).
To interpret this questionnaire, individual scores can range from 0 to 40 with higher scores indicating higher perceived stress.
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4 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exam qualification (0 to 10 punctuation) pondered by the average qualification of the degree
Time Frame: One week after the exam (an only measurement)
|
Between-group differences in the exam qualification (it refers to exam that students will have been visualizing) just before starting the exam.
The qualification of the exam will range from 0 (the worst punctuation) to 10 (perfect punctuation).
In this outcome, the average qualification of the degree for each student will be considered (from the worst, 0 points, to the best, 10 points).
For example, if the student has 8 points as average qualification of the degree and obtains an exam qualification of 9 points, it will be pondered as follows: 9/8 = 1.125.
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One week after the exam (an only measurement)
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Level of current perceived stress
Time Frame: Immediately before the exam
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Between-group differences in the level of perceived stress just at the moment prior to start the exam (10 minutes earlier).
To evaluate it, students will inform about what level of stress they are feeling at that moment (being 0, no stress, and 10 maximal stress).
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Immediately before the exam
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Blood pressure
Time Frame: Immediately before the exam
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Between-group differences in the blood pressure just before starting the exam.
It will be recorded by a healthcare professional by using a stethoscope and registering the systolic and diastolic blood pressure.
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Immediately before the exam
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Maximal heart rate
Time Frame: Immediately before the exam
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Between-group differences in the maximal heart rate just before starting the exam
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Immediately before the exam
|
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Salivary cortisol level
Time Frame: Immediately before the exam
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Between-group differences in the salivary cortisol level just before starting the exam
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Immediately before the exam
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Collaborators and Investigators
Investigators
- Principal Investigator: Natalia Romero-Franco, PhD, University of the Balearic Islands
Publications and helpful links
General Publications
- 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.
- 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.
- 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.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IB4958/22PI
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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