Clinical Trials Directory

Trials / Completed

CompletedNCT02177669

Test-Retest Variability of Quick Contrast Sensitivity Function Testing

Status
Completed
Phase
Study type
Observational
Enrollment
100 (actual)
Sponsor
Nova Southeastern University · Academic / Other
Sex
All
Age
20 Years – 89 Years
Healthy volunteers
Accepted

Summary

The contrast sensitivity function (CSF) provides a comprehensive characterization of spatial vision and predicts functional vision better than visual acuity, but long testing times prevent its psychophysical assessment in clinical applications. Dr. Luis Lesmes et al. (2010) developed the qCSF method to obtain precise CSF measurements in only 30-50 trials using a computerized software program that presents letters on a large monitor that are identified by a patient similar to typical visual acuity testing with an eye chart. The quick CSF method is a Bayesian adaptive method that estimates the full shape of the CSF, and the test duration is only about 3-6 minutes. Some preliminary testing has been performed at other sites with this test in patients with vision loss due to amblyopia and glaucoma, but data from individuals without eye disease who have normal visual acuity has not been systematically collected with the latest version of this test procedure across a wide range of ages. In addition, we aim to gain a better understanding of the typical test-retest variability that is obtained between-sessions that are about a week apart from individuals with good ocular health and visual acuity.

Conditions

Interventions

TypeNameDescription
OTHERquick Contrast Sensitivity Function test

Timeline

Start date
2014-06-01
Primary completion
2016-11-01
Completion
2016-11-01
First posted
2014-06-30
Last updated
2017-04-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02177669. Inclusion in this directory is not an endorsement.