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Peripheral Reading

Factors Limiting Peripheral Reading

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03640130
Enrollment
6
Registered
2018-08-21
Start date
2018-11-01
Completion date
2019-03-01
Last updated
2018-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Central Visual Impairment

Brief summary

The purpose of this study is to evaluate reading performance in the visual periphery by simulating central vision loss using a computer-controlled gaze-contingent display with an eye tracker. Participants will read a page of text at a comfortable rate. Several manipulations hypothesized to improve reading will be tested, such as an inverted-text spotlight of a single word that follows the participant's gaze.

Detailed description

Participants will view paragraphs of multiple sentences of text with their central vision blocked computationally with a simulated scotoma. Participants will be free to move their eyes around the page of text at a comfortable rate. The three outcomes described elsewhere will be evaluated. In different blocks, text will contain one or more of several dynamic assistive manipulations that are hypothesized to enhance reading: 1) inverting the text at a given position, with instructions for the participant to attend to that location, which simulates a surrogate fovea of a patient with central vision loss. 2) horizontally expanding text to alleviate within-word crowding. 3) highlighting the next word with a visible indicator to encourage proper eye movements.

Interventions

BEHAVIORALGaze-contingent text enhancement

In different testing blocks, the efficacy of the different enhancements will be evaluated, such as inverting the text in a gaze-contingent inverted spotlight.

Sponsors

University of Houston
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Normal vision * English language

Exclusion criteria

* Less than 20/20 vision in either eye * Abnormalities which affect vision (amblyopia, keratoconus, etc.) * Ortho-K lenses

Design outcomes

Primary

MeasureTime frameDescription
Reading speedFrom enrollment to completion of testing (<2 weeks)Average time/word it takes to read a paragraph of text.
Reading accuracyFrom enrollment to completion of testing (<2 weeks)Ability to correctly answer comprehension questions or orally read words
Efficiency of eye movementFrom enrollment to completion of testing (<2 weeks)Ability to move the eyes systematically from word to word

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026