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Pilot Study of Virtual Reality Therapy for Students With Anxiety

Pilot Study of Virtual Reality Therapy for Students With Anxiety

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05319509
Enrollment
100
Registered
2022-04-08
Start date
2022-04-01
Completion date
2027-08-01
Last updated
2025-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety

Keywords

virtual reality, college students

Brief summary

The purpose of this study is to assess changes in self-reported anxiety over the course of six virtual reality (VR) sessions and to assess changes in academic self-efficacy, as well as examine the feasibility and acceptability of a relatively short and time intensive VR intervention (i.e.,six sessions over the course of three weeks) for reducing anxiety symptoms in college students.

Interventions

DEVICEgameChange

Staff will explain the rationale behind gameChange, and briefly explain the different scenarios: a doctor's office, a waiting room, a pub, a café, a grocery store, a public street and a bus. Each scenario contains five levels, each increasing with anxiety stimuli and certain tasks the participant must complete. The participant will put on the Oculus headset, and go through a preliminary orientation game. The headset will be casted to an external monitor. Once they start gameChange, it will take the participants to the virtual therapist's room. They will be asked to choose which scenario they would like to participate in first and will complete all five levels for one scenario. Research staff will be taking event sampling-style observations of the participant. After completion of the levels, the participant will return to the virtual therapist's room for debriefing, and then will be asked to exit the game.

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* enrolled in The University of Texas Health Science Center School of Public Health San Antonio regional campus * competent in English * total score of at least 3 on the Generalized Anxiety Disorder (GAD-2)

Exclusion criteria

* Currently receiving psychological treatment for anxiety symptoms, or has received treatment in the last year. * Report photosensitive epilepsy. * Report stereoscopic vision or balance problems

Design outcomes

Primary

MeasureTime frameDescription
Change in physiology such as perspirationWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide
Change in anxiety related behaviors such as LaughterWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide
Change in Psychomotor agitation such as pacingWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide
Change in Psychomotor agitation such as FidgetingWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide
Change in Psychomotor agitation such as Rubbing hands/neck/headWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide
Change in state anxiety as assessed by the Liebowitz Social Anxiety Scale-Self Report version (LSAS-SR)before first session in week 1, before third session in week 2 and before sixth session in week 3The LSAS-SR questionnaire is composed of 24 items divided into 2 subscales, 13 concerning performance anxiety, and 11 pertaining to social situations. The 24 items are first rated on a Likert Scale from 0(none) to 3(severe) on fear felt during the situations, and then the same items are rated from 0(never)-3(usually)regarding avoidance of the situation. Combining the total scores for the Fear and Avoidance sections provides an overall score with a maximum of 144 points. Score of 30 or less indicates social anxiety disorder(SAD) is unlikely, score of 30-60 shows that SAD is probable and score 60-90 indicates that SAD is highly probable.
Change in depressive symptoms as assessed by score on the Patient Health Questionnaire-4 (PHQ-4)Baseline(before the first session in week 1)The PHQ-4 questionnaire consists of 4 questions and each is rated on a 4 point scale from 0(not at all) to 3(every day) for a maximum score of 12,a higher number indicating a worse outcome.
Change in anxiety related behaviors such as rate of speechWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide
Change in anxiety related behaviors such as volume of speechWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide
Change in anxiety related behaviors such as Negative self-talkWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide
Change in anxiety related behaviors such as Utterances about experienceWeek 1(session1 and session 2), week 2( session 3 and session 4), week 3 (session 5 and session 6)Anxiety-related behaviors will be recorded using an event sampling observation guide

Secondary

MeasureTime frameDescription
change in feasibility as assessed by the rating on a short questionnaireafter the third session in week 2 , after sixth session in week 3The usability questionnaire is developed by gameChange about the ease of VR software use, believability of VR environment, and level of engagement. this consists of 5 questions and each one is scored form 1(very difficult) to 5(very easy) for a maximum score of 25, a higher number indicating more easiness in using the VR software
Change in acceptability as assessed by the rating on a short questionnaireafter the third session in week 2 , after sixth session in week 3The usability questionnaire is developed by gameChange about the ease of VR software use, believability of VR environment, and level of engagement. this consists of 5 questions and each is scored form 1(strongly disagree) to 5(strongly agree) for a maximum score of 25
Change in perceived presence in the virtual environment (as indicated by continuous score on the Igroup Presence Questionnaire (IPQ)after the third session in week 2 and the sixth session in week 3There are 14 questions and each one is scored form -3 to +3. A total negative score indicates that the participant personally felt very disconnected from VR world, and that they lacked believable presence within world, and rather felt like they were manipulating a machine from an outside perspective.
Change in self-reported academic performance as assessed by the Motivated Strategies for Learning Questionnaire (MSLQ)before first session in week 1, before third session in week 2 and before sixth session in week 3The MSLQ questionnaire consists of 9 questions each one is scored from 1= not at all true of me to 7=very true of me, a higher number indicating a better outcome with a maximum score of 63

Countries

United States

Contacts

Primary ContactTsai Jack, PhD
Jack.Tsai@uth.tmc.edu210-276-9022
Backup ContactAbigail Lipe
Abigail.R.Lipe@uth.tmc.edu210-722-8218

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026