NCT05419713

Brief Summary

The ability to judge the locations of various objects from oneself during self-motion in the intermediate distance range (\~2-25m) is crucial for successful performance of activities of daily living, such as walking and driving. However, little is known about the mechanisms of visual space perception involved in judging distance, the focus of this project, in the planning and/or execution of self-motion in the natural 3D environment. The theoretical knowledge to be gained from this project will contribute to the scientific literature and provide insights into how eye and neurological defects could impair visual space perception, wayfinding, and mobility.

Trial Health

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Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
180

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2021

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
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 Start

First participant enrolled

September 30, 2021

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

June 1, 2022

Completed
14 days until next milestone

First Posted

Study publicly available on registry

June 15, 2022

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2025

Completed
Last Updated

September 25, 2024

Status Verified

September 1, 2024

Enrollment Period

3.8 years

First QC Date

June 1, 2022

Last Update Submit

September 23, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • Visual mechanisms of intermediate distance space perception (distance) before and after self-motion

    Subjects will judge perceived distances (cm) of test targets from themselves before self-motion to establish a baseline measure. Subjects will then undergo self-motion for an average of 10 sec, and stop at a predetermined location. Then subjects will again judge the perceived distance (cm) of test targets after the self-motion. The change in perceived distance (cm) from baseline will reveal if their perception is affected by environmental factors, internal perceptual process and/or cognitive process.

    During procedure, an average of 10 sec.

  • Visual mechanisms of intermediate distance space perception (height) before and after self-motion.

    Subjects will judge perceived heights (cm) of test targets relative to the floor or ceiling before self-motion to establish a baseline measure. Subjects will then undergo self-motion for an average of 10 sec, and stop at a predetermined location. Then subjects will again judge the perceived height (cm) of test targets after the self-motion. The change in perceived height (cm) from baseline will reveal if their perception is affected by environmental factors, internal perceptual process and/or cognitive process.

    Druing procedure, an average of 10 sec.

Study Arms (1)

Visual scences

EXPERIMENTAL

Lit target locations in visual environment will be varied and subjects' perceived locations will be measured.

Other: Visual Stimuli for Space Perception

Interventions

The visual environment (e.g., target locations and texture backgrounds) will be varied and human behavioral responses (judged distances) will be measured to reveal the space perception and cognitive processes underlying space perception and navigation.

Visual scences

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Adults (up to 40 years of age)
  • Children (18 years and older)
  • Normal, or corrected-to-normal, visual acuity (at least 20/20)
  • Stereo acuity (\<20 arc sec).

You may not qualify if:

  • Self-reported history of visual and eye diseases
  • Physical movement restrictions.
  • Vulnerable populations such as pregnant women will be excluded owing to the extensive time commitment required of the subjects.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Louisville

Louisville, Kentucky, 49292, United States

RECRUITING

Study Officials

  • Zijiang He

    University of Louisville

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Zijiang He, Ph.D.

CONTACT

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
Professor

Study Record Dates

First Submitted

June 1, 2022

First Posted

June 15, 2022

Study Start

September 30, 2021

Primary Completion

June 30, 2025

Study Completion

June 30, 2025

Last Updated

September 25, 2024

Record last verified: 2024-09

Locations