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RecruitingNCT07216534Updated Jun 22, 2026

Virtual Reality Viewing of Unaltered Streetscape Versus Digitally Manipulated Opposite Streetscape to Assess Psychosocial Response in Participants

An interventional study of Survey Administration and Virtual Technology Intervention in Hematopoietic and Lymphatic System Neoplasm, Malignant Solid Neoplasm and Psychiatric Disorder, sponsored by Ohio State University Comprehensive Cancer Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-22.

Sponsored by Ohio State University Comprehensive Cancer Center · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This clinical trial compares virtual reality viewing of an unaltered streetscape versus a digitally manipulated opposite streetscape to assess the psychosocial response in participants. Visible measures of neighborhood factors might be associated with health outcomes and risk factors of those outcomes. Short-term exposure to virtual reality environments representing very high or very low levels of neighborhood physical disorder - presence or absence of garbage/litter, presence or absence of graffiti, presence or absence of an abandoned building, presence or absence of large dumpsters, poor or very well-kept building conditions, poor or very well-kept yard conditions, poor or very well-kept road verge conditions may be a safe and effective way to assess psychosocial response in participants.

Read the detailed description

PRIMARY OBJECTIVES:

I. Compare sympathetic autonomic measures (heart rate variability and skin conductance) between participants viewing, in virtual reality, their streetscape as a digitally manipulated opposite version with respect to physical disorder indicators versus participants viewing their streetscape as a digital twin with respect to physical disorder indicators.

II. Compare self-report measures (Self-Assessment Manikin and state anxiety ratings) between participants viewing, in virtual reality, their streetscape as a digitally manipulated opposite version with respect to physical disorder indicators versus participants viewing their streetscape as a digital twin with respect to physical disorder indicators.

III. Record side effects of interacting within a virtual reality environment over short periods of time (3-5 min):

IIIa. Quantify frequency of side effects; IIIb. Explore whether side effects increase across subsequent VR sessions of the cross-over study; IIIc. Explore whether side effects vary by VR intervention arm (digital twin of own streetscape or digitally manipulated opposite indicators of physical disorder of own streetscape).

IV. Analyze impact of covariates on study outcomes.

EXPLORATORY OBJECTIVES:

I. Compare eye gaze density between participants viewing, in virtual reality, their streetscape as a digitally manipulated opposite version with respect to physical disorder indicators versus participants viewing their streetscape as a digital twin with respect to physical disorder indicators.

II. Compare self-report measures (neighborhood social cohesion and neighborhood disorder) between participants viewing, in virtual reality, their streetscape as a digitally manipulated opposite version with respect to physical disorder indicators versus participants viewing their streetscape as a digital twin with respect to physical disorder indicators.

OUTLINE: Participants are randomized within their residing neighborhood to 1 of 2 arms.

ARM I: Participants have their streetscape photographed. Participants view a standard residential streetscape using virtual reality (VR) for up to 5 minutes. Patients then view a digital twin of their streetscape with identical physical disorder using VR for up to 5 minutes followed by viewing their streetscape with the opposite physical disorder using VR for up to 5 minutes.

ARM II: Participants have their streetscape photographed. Participants view a standard residential streetscape using VR for up to 5 minutes. Patients then view their streetscape with the opposite physical disorder using VR for up to 5 minutes followed by viewing a digital twin of their streetscape with identical physical disorder using VR for up to 5 minutes.

02

Conditions studied

  • Hematopoietic and Lymphatic System Neoplasm
  • Malignant Solid Neoplasm
  • Psychiatric Disorder

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03

In context

Mental Disorders

2,107 studies on the registry are indexed under Mental Disorders; 416 are open to participants now.

This study's planned enrollment of 32 is below the median of 94 across 1,574 interventional studies indexed under Mental Disorders.

Browse Mental Disorders studies →

Lead sponsor

Ohio State University Comprehensive Cancer Center is the lead sponsor of 369 studies on the registry; 81 are open to participants now.

Of its 38 completed or terminated interventional studies of FDA-regulated products, 19 (50%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Adults 18+
  • Must currently live (4+ night/week) at the residence being studied. Only one resident per household will be selected
  • Must understand and be able to read English
  • Must agree to have residence photographed
  • Must be able to wear a VR head mounted display
  • Must live in neighborhood that has been selected for study
  • Must be willing and able to attend an approximately 2 hour in-person visit on Ohio State University (OSU) campus

Exclusion criteria

Exclusion Criteria:

  • Pregnant women
  • Visual or mobility impairment
  • Cannot have epilepsy or other condition that would inhibit them from being able to use a VR headset
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
32 participants (estimated)

Study arms

  • Experimental
    Arm I (twin followed by opposite streetscape)

    Participants have their streetscape photographed. Participants view a standard residential streetscape using VR for up to 5 minutes. Patients then view a digital twin of their streetscape with identical physical disorder using VR for up to 5 minutes followed by viewing their streetscape with the opposite physical disorder using VR for up to 5 minutes.

    Other: Survey Administration · Other: Virtual Technology Intervention

  • Experimental
    Arm II (opposite followed by twin streetscape)

    Participants have their streetscape photographed. Participants view a standard residential streetscape using VR for up to 5 minutes. Patients then view their streetscape with the opposite physical disorder using VR for up to 5 minutes followed by viewing a digital twin of their streetscape with identical physical disorder using VR for up to 5 minutes.

    Other: Survey Administration · Other: Virtual Technology Intervention

Interventions

  • OtherSurvey Administration

    Ancillary studies

  • OtherVirtual Technology Intervention

    View standard streetscape

    Also known as: Virtual Reality Intervention, Virtual Technology

  • OtherVirtual Technology Intervention

    View digital twin of streetscape

    Also known as: Virtual Reality Intervention, Virtual Technology

  • OtherVirtual Technology Intervention

    View opposite digital streetscape

    Also known as: Virtual Reality Intervention, Virtual Technology

06

What researchers measure

Primary outcomes

  1. Change in heart rate variability

    Mean heart rate variability over the entire session of each VR condition will be calculated from electrocardiograph data. Will compare the difference between two VR conditions (viewing opposite neighborhood image versus viewing twin neighborhood image) using a crossover design. Analyses of outcomes will be conducted using generalized linear mixed model approaches.

    Time frame: From baseline to completion of virtual reality (VR) viewings, up to 1 day

  2. Change in skin conductance

    Skin conductance, measured as microsiemens, will be calculated as the mean value over each VR condition. Will compare the difference between two VR conditions (viewing opposite neighborhood image versus viewing twin neighborhood image) using a crossover design. Analyses of outcomes will be conducted using generalized linear mixed model approaches.

    Time frame: From baseline to completion of VR viewings, up to 1 day

  3. Affective reaction

    Assessed via Self-assessment Manikin. Will compare the difference between two VR conditions (viewing opposite neighborhood image versus viewing twin neighborhood image) using a crossover design. Analyses of outcomes will be conducted using generalized linear mixed model approaches.

    Time frame: After completion of VR viewings, up to 1 day

  4. Anxiety

    Assessed via Spielberger State-Trait Anxiety Inventory short form. Will compare the difference between two VR conditions (viewing opposite neighborhood image versus viewing twin neighborhood image) using a crossover design. Analyses of outcomes will be conducted using generalized linear mixed model approaches.

    Time frame: After completion of VR viewings, up to 1 day

  5. Participant reported discomfort

    This is an open-ended outcome measure. Discomfort reported by participants will be recorded by study staff.

    Time frame: After completion of VR viewings, up to 1 day

07

Study locations

1 of 1 sites recruiting
  • Ohio State University Comprehensive Cancer Center
    Columbus, Ohio 43210, United States
    • Jesse Plascak, PhD, MPH · Contact · 614-293-8024
    • Jesse Plascak, PhD, MPH · Principal investigator
    Recruiting
08

References and documents

Related links

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07216534
Lead sponsor
Ohio State University Comprehensive Cancer Center
Responsible party
Jesse Plascak (Principal Investigator, Ohio State University Comprehensive Cancer Center) — Principal investigator
First posted
Oct 14, 2025
Start date
Sep 1, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Jun 22, 2026

Study contacts

The Ohio State University Comprehensive Cancer Center
Contact
OSUCCCClinicaltrials@osumc.edu
800-293-5066
Jesse Plascak, PhD, MPH
principal investigator · Ohio State University Comprehensive Cancer Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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