NCT05141604

Brief Summary

The investigators are developing a new test of pedestrian hazard detection in virtual reality (VR) head-mounted display (HMD) headset, which shows virtual oncoming pedestrians in 3D while subjects are walking in real-world environment, for evaluation of visual field expansion to improve mobility in people with visual field loss.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
15

participants targeted

Target at below P25 for not_applicable

Timeline
1mo left

Started May 2022

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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 Progress98%
May 2022May 2026

First Submitted

Initial submission to the registry

November 19, 2021

Completed
13 days until next milestone

First Posted

Study publicly available on registry

December 2, 2021

Completed
6 months until next milestone

Study Start

First participant enrolled

May 17, 2022

Completed
3.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 30, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2026

Expected
Last Updated

October 24, 2025

Status Verified

October 1, 2025

Enrollment Period

3.9 years

First QC Date

November 19, 2021

Last Update Submit

October 22, 2025

Conditions

Keywords

walkingcollisionfield expansionvisual field loss

Outcome Measures

Primary Outcomes (1)

  • Response time

    During the pedestrian detection task, average response time to the colliding pedestrian with and without prisms

    Through study completion, an average of four months

Secondary Outcomes (4)

  • Head movement range

    Through study completion, an average of four months

  • Walking speed

    Through study completion, an average of four months

  • Pedestrian detection rate

    Through study completion, an average of four months

  • Error rate

    Through study completion, an average of four months

Study Arms (1)

Field expansion view

EXPERIMENTAL

Various configurations of field expansion views will be additionally displayed on HMD

Other: Field expansion view

Interventions

Overlaid small window on HMD to show the part of the scene in the blind field into portions of the participants' remaining, seeing, field of vision

Field expansion view

Eligibility Criteria

Age14 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • At least 14 years of age (no upper age limit)
  • In sufficiently good health to be able to complete sessions lasting 2-3 hours
  • Able to understand English
  • Able to give voluntary, informed consent
  • Able to independently move short distances
  • Binocular vision parameters within normal limits (Stereopsis ≤ 100 arc sec on any stereo test)
  • Visual field loss, either peripheral field loss (\<30 degrees diameter) or hemianopic field loss (blind in half of visual field)
  • Better than 20/100 visual acuity in the worse eye

You may not qualify if:

  • Patients with any self-reported physical or mental disabilities, including cognitive dysfunction, balance problems, or other deficits that could impair their ability to respond to the stimuli presented in this study
  • Any person with a self-reported medical history (such as pacemaker use or photosensitive epilepsy) or physical condition listed on the device manual of the Oculus / HMD system used for the experiment as a contraindication
  • Any self-reported history of seizures (any type) in the last 6 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Schepens Eye Research Institute

Boston, Massachusetts, 02114, United States

Location

MeSH Terms

Conditions

Hemianopsia

Condition Hierarchy (Ancestors)

Vision DisordersSensation DisordersNeurologic ManifestationsNervous System DiseasesBlindnessEye DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Eli Peli, OD, MSc

    Senior Scientist

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Senior Scientist

Study Record Dates

First Submitted

November 19, 2021

First Posted

December 2, 2021

Study Start

May 17, 2022

Primary Completion

March 30, 2026

Study Completion (Estimated)

May 31, 2026

Last Updated

October 24, 2025

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations