NCT07770880

Brief Summary

The purpose of this study is to examine whether repeated exposure to an active shooter or target practice virtual reality (VR) scenario alters physiological and psychological stress responses over time. Specifically, this study will determine whether the pattern and magnitude of stress habituation differ between the two VR conditions.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2026

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

August 13, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 18, 2026

Completed
Last Updated

August 18, 2026

Status Verified

August 1, 2026

Enrollment Period

7 months

First QC Date

August 13, 2026

Last Update Submit

August 13, 2026

Conditions

Keywords

StressStress biomarkersSalivary Alpha-Amylase (sAA)Salivary Secretory Immunoglobulin A (SIgA)Acute stressState Anxiety Inventory (SAI) scaleActive shooterVirtual Reality (VR) trainingLaw enforcement trainingTarget practice

Outcome Measures

Primary Outcomes (4)

  • State Anxiety Inventory (SAI)

    The SAI is a 6 question survey on a 24 point scale, asking the subject to record how they feel. Questions asked were "I am calm," I am tense," "I am worried," "I am relaxed," etc. Subjects were asked to fill this out 4 times throughout the study, alongside HR and saliva samples.

    Timepoint 1-4 were 20 minutes pre, immediately pre, immediately post, and 15 minutes post

  • Heart Rate

    Heart rate was recorded immediately prior to each saliva sample using a Polar Verity Sense heart rate wrist/arm strap.

    HR was recorded 4 times, before each saliva sample period

  • Secretory Immunoglobulin-A

    SIgA is a marker of immune function and salivary SIgA concentrations tend to increase when exposed to stress

    Measured using the saliva samples taken at timepoints 1-4 (20 min pre, immediately pre, immediately post, 15 min post)

  • Salivary Alpha Amylase

    sAA is an enzyme involved in digestive processes. Amylase concentrations in saliva have been shown to reflect sympathetic stress. Thus, as sympathetic stress increases, salivary amylase concentrations tend to increase.

    Measured using the saliva samples taken at timepoints 1-4 (20 min pre, immediately pre, immediately post, 15 min post)

Study Arms (2)

Active Shooter

EXPERIMENTAL

Group assigned to active shooter scenarios only

Other: Active Shooter

Target Practice

EXPERIMENTAL

Group assigned to two target practice scenarios and one active shooter scenario for the third trial only.

Other: Target Practice

Interventions

Participants experienced a virtual reality simulation lasting \~3 minutes. Participants took on the roll of a law enforcement officer responding to an active shooter situation in a gas station (trial 1), home (trial 2), and school (trial 3).

Active Shooter

Participants experienced a virtual reality simulation lasting \~3 minutes. Participants had two trials of target practice training and one trial of an active shooter scenario where they responded as a law enforcement officer in a school.

Target Practice

Eligibility Criteria

Age18 Years - 39 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Generally healthy
  • Between the ages of 18-39
  • Student at texas state

You may not qualify if:

  • No known cardiovascular or metabolic diseases
  • Free from a major stressor in the last 30 days (recent divorce, birth of child, miscarriage, etc.)
  • Not currently taking medication that can impact results (e.g., psychiatric medication typically prescribed for psychological disorders such as depression, anxiety, etc.)
  • Must also be free from any known psychiatric or physical illness (e.g., diabetes, myocardial infarction, stroke, Alzheimer's disease, alcoholism, epilepsy, severe motion sickness, etc.).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Texas State University

San Marcos, Texas, 78666, United States

Location

MeSH Terms

Conditions

Stress Disorders, Traumatic, Acute

Interventions

Mass Shooting Events

Condition Hierarchy (Ancestors)

Stress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

Intervention Hierarchy (Ancestors)

Mass Casualty IncidentsDisastersEnvironmentEnvironment and Public Health

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Subjects were randomly assigned to one of two groups, active shooter (AS) or target practice (TP).
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

August 13, 2026

First Posted

August 18, 2026

Study Start

October 1, 2025

Primary Completion

May 1, 2026

Study Completion

May 1, 2026

Last Updated

August 18, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

IRB at Texas State does not allow the sharing of individual data, and all data has already been made unidentifiable for this study.

Locations