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Enrolling by invitation NCT07314788

Empathy and Virtual Reality (VR)

No phase Interventional Virtual Reality Fear

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Fear-inducing Virtual Reality (VR) experience, Neutral Virtual Reality (VR) experience.
Who it may be relevant to
Registry conditions: Virtual Reality, Fear. Basic parameters: 18 years — 25 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study will characterize the subjective and physiological changes associated with empathy following a fear-inducing virtual reality (VR) experience.

Interventions

  • Behavioral Fear-inducing Virtual Reality (VR) experience
    Participants will complete a single virtual reality (VR) exposure involving a fear-inducing scenario (e.g., walking a plank above a high-rise building or canyon).
  • Behavioral Neutral Virtual Reality (VR) experience
    Participants will complete a single virtual reality (VR) exposure involving a fear-inducing scenario (e.g., walking to the edge of a curb at street level).

Primary outcome measures

  • Change in self-reported empathy scores [Time frame: Baseline (prior to VR experience) and approximately 5 minutes post-VR experience.]
  • Change in heart rate [Time frame: Baseline (prior to VR experience) and approximately 5 minutes post-VR experience.]
Secondary outcome measures (1)
  • Change in the correlation between self-reported anxiety scores of self and another [Time frame: Baseline (prior to VR experience) and approximately 5 minutes post-VR experience.]

Eligibility criteria

Inclusion criteria

  • College-aged adults (18-25 years old)
  • English-speaking
  • Normal or corrected vision.
  • Able to provide consent.

Exclusion criteria

  • Presence of a significant and/or unstable medical illness (e.g., cardiovascular disease, cancer, neurological disorder) or head trauma (e.g., concussion).

Additional exclusion criteria apply to virtual reality (VR):

  • VR contraindications: epilepsy, migraines, flu, sleep deprivation, etc.
  • More than minimal VR experience assessed via self-report (e.g., How often have you used virtual reality in the past? 0=never, 6=very frequently)
  • Extreme phobia of heights and/or spiders will be assessed using Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) specific phobia subscale.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Basic science

Study locations

United States · 1 center
  • University of Miami — Coral Gables

Identifiers

NCT: NCT07314788 · 20241195

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗