- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05251155
Accuracy of Mobile-Based Vision Charts.
March 13, 2022 updated by: Ahmed Abdelshafy, Benha University
Accuracy of Mobile-Based Vision Charts in Clinical Practice.
Analyzing the accuracy of mobile-based distant vision charts in clinical practice as an economic alternative for standard vision charts.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Accuracy of mobile-based visual acuity testing in clinical practice is still debatable.
The aim of this study was to analyze the accuracy of mobile-based distant vision chart in comparison to standard chart projector.
Study Type
Observational
Enrollment (Actual)
288
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
QA
-
Banhā, QA, Egypt, 13511
- Al-Nil Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
4 years to 70 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Subjects aimed to asses their best corrected visual acuity or seek spectacles prescription at ophthalmology clinic at Al-Nil Hospital, Banha, EGYPT.
Description
Inclusion Criteria:
- Subjects visited ophthalmology clinic at Al-Nil Hospital, Banha, EGYPT for visual acuity assessment.
- Subjects that their best corrected visual acuity was ranged from 0.1 to 1.0 in decimal form measured on snellen's chart.
Exclusion Criteria:
- Subjects that refuse to measure visual acuity twice during the same visit.
- Subjects that their best corrected visual acuity is less than 0.1 in decimal form by the standard chart projector.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Standard vision chart.
Best corrected visual acuity measured by standard chart projector.
|
Measuring distant visual acuity on snellen's chart using two methods and results were converted to equivalent logarithm of minimum angle of resolution to compare accuracy of mobile based chart to the standard vision chart.
|
|
Mobile based vision chart.
Best corrected visual acuity measured by mobile based chart with screen mirroring over 24 inch monitor.
|
Measuring distant visual acuity on snellen's chart using two methods and results were converted to equivalent logarithm of minimum angle of resolution to compare accuracy of mobile based chart to the standard vision chart.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Accuracy of mobile based "snellen chart" in measuring distant visual acuity.
Time Frame: Immediately after visual acuity testing using the standard chart projector.
|
To compare the decimal results of mobile based snellen chart for measuring distant vision with the decimal results of the standard snellen chart projector.
|
Immediately after visual acuity testing using the standard chart projector.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ahmed A Abdelshafy, MD, Benha University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2020
Primary Completion (Actual)
April 11, 2021
Study Completion (Actual)
July 21, 2021
Study Registration Dates
First Submitted
February 10, 2022
First Submitted That Met QC Criteria
February 18, 2022
First Posted (Actual)
February 22, 2022
Study Record Updates
Last Update Posted (Actual)
March 29, 2022
Last Update Submitted That Met QC Criteria
March 13, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- RC-15-2-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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