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| Sponsor: | American Optometric Association |
|---|---|
| Information provided by: | American Optometric Association |
| ClinicalTrials.gov Identifier: | NCT00317525 |
Purpose
The aim of this study is to examine the relationship between optical blur from poor refractive corrections (glasses) of older workers using computers and their productivity and comfort in the workplace. The investigators believe that improving the visual status of subjects who use computers will have a beneficial effect on productivity and visual comfort.
| Condition | Intervention | Phase |
|---|---|---|
|
Refractive Errors Asthenopia |
Device: Spectacle Lenses |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Factorial Assignment, Efficacy Study |
| Official Title: | Effects of Different Add Powers on the Comfort and Productivity of Computer Users With Fixed or Free Head Movement |
| Estimated Enrollment: | 36 |
| Study Start Date: | May 2005 |
| Estimated Study Completion Date: | June 2006 |
The aim of this study is to examine the relationship between optical blur from poor refractive corrections (glasses) of older workers using computers and their productivity and comfort in the workplace. We believe that improving the visual status of subjects who use computers will have a beneficial effect on productivity and visual comfort. All subjects will be required to complete a vision screening at no charge to decide if they qualify for the study. This is a double-blind study, which means that neither the subject nor the doctors will know which pair of lenses you will be wearing during the parts of the study. Subjects will complete a total of 4 hours of testing. The total amount of testing will be divided into ten 15-minute periods. During each period, the investigator will place different lenses in a trial frame. The trial frame that the subject will wear during the experiment will have their prescription for near plus an unknown pair of lenses. During the testing, the subject will complete a task involving finding and deleting apostrophes from a manuscript on a standard computer. Either the investigator or co-investigator will explain how to do this simple task. Subjects will answer a short survey before and after these tasks to check on symptoms resulting from using the computer. The following periodic measurements will be made during the study: productivity and accuracy to search for apostrophes (‘) in a document on one of the states of the U.S. These tasks will require a total of 4 hours testing with a total of ten pairs of trial lenses during a single visit.
Eligibility| Ages Eligible for Study: | 40 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Contacts and Locations| United States, Alabama | |
| School of Optometry | |
| Birmingham, Alabama, United States, 35294-0010 | |
| Principal Investigator: | Kent M Daum, O.D., Ph.D. | School of Optometry, University of Alabama at Birmingham |
More Information
| Study ID Numbers: | X050314015 |
| Study First Received: | April 21, 2006 |
| Last Updated: | September 7, 2006 |
| ClinicalTrials.gov Identifier: | NCT00317525 History of Changes |
| Health Authority: | United States: Institutional Review Board |
|
Refractive error Asthenopia |
|
Eye Diseases Asthenopia Refractive Errors |