Effects of Optical Blur on Performance and Comfort of Computer Users

The recruitment status of this study is unknown because the information has not been verified recently.
Verified April 2006 by Vision Council of America.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Vision Council of America
ClinicalTrials.gov Identifier:
NCT00318045
First received: April 21, 2006
Last updated: NA
Last verified: April 2006
History: No changes posted
  Purpose

The aim of this study is to examine the relationship between optical blur from poor refractive corrections (glasses) of 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.


Condition Intervention Phase
Refractive Error
Device: Eyeglass lenses
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Official Title: Effects of Optical Blur on Performance and Comfort of Computer Users

Resource links provided by NLM:


Further study details as provided by Vision Council of America:

Primary Outcome Measures:
  • Visual comfort
  • Productivity (correct output per hour)

Estimated Enrollment: 35
Study Start Date: October 2005
Estimated Study Completion Date: April 2006
Detailed Description:

The aim of this study is to examine the relationship between optical blur from poor refractive corrections (glasses) of 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 you qualify for the study. Subjects will select a frame to be worn during the period of the study. Subjects will wear either your best correction or your present prescription in the frame for a period of 1-month. This will be a double-blind study, which means that neither the subject nor your doctors will know which pair of glasses the subjects will be wearing during the parts of the study. Subjects will complete 4 hours of testing during the first period (4 weeks) then the lenses will be switched for the second period (4 weeks). During the testing, subjects will complete two tasks on a standard computer. Either the investigator or co-investigator will explain to you how to do these simple tasks. One of these tasks will involve looking at printed material and entering correct information into the computer. The other task involves finding and deleting apostrophes from a manuscript on the computer. All subjects will answer a short survey before and after these tasks to check on symptoms resulting from using the computer. Before and after each period, the subjects also will answer another survey to measure their visual functioning using these glasses.

The following periodic measurements will be made during the study: productivity and accuracy to enter a list of state populations, and a search for apostrophes (‘) in a document on one of the states of the U.S. These tasks will require 4 hours testing with each of the two pairs of trial glasses for two periods (each period lasts for one month). Subjects will be asked to return to the clinic for 4 hrs during the first 4-week period and for 4 more hrs during the second 4-week period. At each visit subjects will be asked if they have experienced any undesirable reactions and will complete a short survey.

Subjects will also be required to complete a short 9-question survey to determine their visual comfort before and after 1-hour of work on their own computer at your home or job during each 1-month period of the study. These short phone surveys will take less than 5-minutes to complete and will be arranged at the subject’s convenience before and after the subjects are going to be working on your computer for at least 1-hr. This survey will be repeated on five occasions. Finally, 3-months after the experimental portion of the study is completed, all subjects will be required to also answer the same short 9-question survey as you work on your computer. This will also be a phone survey and will be completed on three occasions before and after 1-hr of work on their own computer at home or job.

  Eligibility

Ages Eligible for Study:   19 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • 19 yrs of age or more
  • Use a computer for 1 hr per day or more
  • 20/40 or better visual acuity in each eye

Exclusion Criteria:

  • None
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00318045

Locations
United States, Alabama
School of Optometry
Birmingham, Alabama, United States, 35294-0010
Sponsors and Collaborators
Vision Council of America
Investigators
Principal Investigator: Kent M. Daum, O.D., Ph.D. School of Optometry, University of Alabama at Birmingham
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00318045     History of Changes
Other Study ID Numbers: X050208014
Study First Received: April 21, 2006
Last Updated: April 21, 2006
Health Authority: United States: Institutional Review Board

Keywords provided by Vision Council of America:
Refractive error
Asthenopia

Additional relevant MeSH terms:
Refractive Errors
Eye Diseases

ClinicalTrials.gov processed this record on September 14, 2014