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CompletedNCT04936100Updated Jul 27, 2022

Assessment of the Validity, Reliability, and Feasibility of Two Smartphone Applications for Testing the Visual Acuity

An interventional study of Assessment of distance and near visual acuity using "Vision Screening module" of "Easy Vision" application and Assessment of distance and near visual acuity using "Test Yourself module" of "Easy Vision" application in Vision Impairment and Blindness, sponsored by Shahid Beheshti University of Medical Sciences. Completed at 1 site in Iran, Islamic Republic of. Open to participants aged 10 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-07-27.

Sponsored by Shahid Beheshti University of Medical Sciences · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
10 Years and older
Sex
All
01

Study summary

Visual acuity (VA) is the most common measure of visual function globally. In clinical settings and during screening events, VA is an important measure to quantify changes in vision over time. Additionally, in the context of epidemiological studies and population-based surveys, VA is a critical measure to determine the presence and degree of vision impairment and to report on the indicators of effective eye care service coverage (i.e. refractive error and cataract surgery), that are currently considered by World Health Organization (WHO) for monitoring progress towards the Universal Health Coverage.

There are numerous applications for assessing VA; however, the number of validated applications is limited. In this study, the investigators aim to evaluate the external validity, intra- and inter-observer reliability, and feasibility of two applications ("Easy Vision" and "Peek Acuity") for testing the visual acuity.

02

Conditions studied

  • Vision Impairment
  • Blindness

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Keywords

  • Visual acuity
  • Smartphone
03

In context

Blindness

161 studies on the registry are indexed under Blindness; 33 are open to participants now.

This study's enrollment of 120 is above the median of 30 across 105 interventional studies indexed under Blindness.

Browse Blindness studies →

Lead sponsor

Shahid Beheshti University of Medical Sciences is the lead sponsor of 221 studies on the registry; 19 are open to participants now.

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

04

Who can participate

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

Inclusion criteria

  • Age ≥10 years old

Exclusion criteria

Exclusion criteria:

  • Subjects who are not able to respond to the examiner
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
120 participants (actual)

Study arms

  • Experimental
    Visual acuity assessment using "Vision Screening module" of "Easy Vision" application

    Device: Assessment of distance and near visual acuity using "Vision Screening module" of "Easy Vision" application

  • Experimental
    Visual acuity assessment using "Test Yourself module" of "Easy Vision" application

    Device: Assessment of distance and near visual acuity using "Test Yourself module" of "Easy Vision" application

  • Experimental
    Visual acuity assessment using "Peek Acuity" application

    Device: Assessment of distance and near visual acuity using "Peek Acuity" application

  • Other
    Visual acuity assessment using the conventional methods

    Other: Assessment of distance and near visual acuity using the conventional methods

Interventions

  • DeviceAssessment of distance and near visual acuity using "Vision Screening module" of "Easy Vision" application

    The presenting visual acuity will be assessed using the Vision Screening module of the "Easy Vision" application.

  • DeviceAssessment of distance and near visual acuity using "Test Yourself module" of "Easy Vision" application

    The presenting visual acuity will be assessed using the Test Yourself module of the "Easy Vision" application.

  • DeviceAssessment of distance and near visual acuity using "Peek Acuity" application

    The presenting visual acuity will be assessed using the "Peek Acuity" application.

  • OtherAssessment of distance and near visual acuity using the conventional methods

    The presenting visual acuity will be assessed using the conventional methods \["Chart: Tumbling E optotype" for assessing distance visual acuity and "Handheld chart: Tumbling E Near Point Vision Chart" for assessing near visual acuity\]

06

What researchers measure

Primary outcomes

  1. Distance visual acuity assessment with Easy Vision versus Peek Acuity versus conventional distance visual acuity chart

    To assess the agreement between two smartphone-based evaluation of distance visual acuity (LogMAR unit) with Easy Vision and Peek Acuity and a conventional distance visual acuity chart (Tumbling E optotype)

    Time frame: Through study completion [an average of 6 months]

  2. Near visual acuity assessment with Easy Vision versus Peek Acuity versus conventional near visual acuity chart

    To assess the agreement between two smartphone-based evaluation of near visual acuity (LogMAR unit) with Easy Vision and Peek Acuity and a conventional near visual acuity chart (Handheld chart: Tumbling E Near Point Vision Chart)

    Time frame: Through study completion [an average of 6 months]

07

Study locations

1 site
  • Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences
    Tehran, Iran, Islamic Republic of
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 27, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04936100
Lead sponsor
Shahid Beheshti University of Medical Sciences
Responsible party
Zahra Rabbani Khah (Head of Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences) — Principal investigator
First posted
Jun 23, 2021
Start date
Jun 23, 2021
Primary completion
Dec 23, 2021
Completion
Jan 30, 2022
Last update
Jul 27, 2022

Oversight

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

Not currently enrolling

This study is completed, as verified in Apr 2021. You cannot join it, but the record below documents what was studied.

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