Randomized Clinical Trial of Bifocal Lenses Versus Computer-specific Progressive Addition Lenses

• ClinicalTrials.gov Identifier: NCT00585026
• Recruitment Status: Terminated
• First Posted: January 2, 2008
• Last Update Posted: June 15, 2011
• Sponsor: University of Alabama at Birmingham
• Information provided by: University of Alabama at Birmingham

Study Description

Brief Summary:

This is a research study designed to test the utility of D-shaped bifocal lenses and PRIO Computer Lenses for persons using a computer. We hypothesize that lenses specially designed for computer use may allow more comfortable and productive work on a computer.

Condition or disease	Intervention/treatment	Phase
Refractive Error; Presbyopia; Asthenopia; Eyeglasses	Device: D-28 bifocal lenses and frame; Device: Progressive addition computer lenses and frame	Phase 3

Detailed Description:

This is a research study designed to test the utility of D-shaped bifocal lenses and PRIO Computer Lenses for persons using a computer. These are different types of eyeglass lenses and are commonly used when performing computer work. D-shaped bifocal lenses are designed for general purpose use and PRIO Computer Lenses are progressive addition lenses designed for using a computer and are not useful for driving or other tasks requiring clear distance vision. The study will examine how much work a subject completes during a 2-hr visit to the laboratory (productivity) and how a subject feels when working (symptoms). The UAB Department of Optometry sponsors this research study. Interested individuals must be at least 40 years of age and have relatively good vision in each eye when wearing glasses and to do at least 4-hrs of computer work per workday. There are no other restrictions to enter the study.

Participating subjects will be provided one of two different types of lenses and a choice of eyeglass frames. All subjects will be required to use the pair of glasses provided for all computer work for a period of 4 months. During the fourth and eighth weeks of this period, subjects will be required to complete three short surveys over the phone (10 questions) a day for five days (morning, noon and afternoon) on how the glasses affect their work on a computer and how they feel. These surveys should take about 5 minutes or less to complete. During the fifth or sixth week, subjects would be required to visit the laboratory at the School of Optometry to do 2-hours of editing tasks on a computer and complete the same short survey before beginning and after finishing. Participants would be called once a week to confirm that they are wearing the glasses. These calls would last about 2-3 minutes or less.

Upon qualifying for the study, subjects will be randomly (like the flip of a coin) assigned by a computer to receive either the bifocal lenses or the variable focus computer glasses. This will be a single-blind study, which means that neither your doctors completing the survey and the on-site visit will not be informed which type of glasses the subject is using.

The following periodic measurements will be made during the study: visual and upper extremity comfort (surveys) and productivity (editing task). Subjects will be asked to return to the clinic for 1 2-hr visit. At each visit subjects will be asked if they have experienced any undesirable reactions and how they are tolerating the glasses.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 40 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Single
• Primary Purpose: Treatment
• Official Title: Randomized Clinical Trial of Bifocal Lenses Versus Computer-specific Progressive Addition Lenses on Symptoms and Performance on a Computer
• Study Start Date: October 2006
• Actual Study Completion Date: June 2007

Arms and Interventions

Outcome Measures

Primary Outcome Measures :

1. visual comfort index
2. productivity (correct words edited per hour)

Eligibility Criteria

• Ages Eligible for Study: 40 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

Inclusion Criteria:

• 40 yrs of age or greater
• 20/40 or better corrected visual acuity in each eye
• 4 hrs or more of computer use per workday

Exclusion Criteria:

• None

Contacts and Locations

Locations

United States, Alabama

School of Optometry

Birmingham, Alabama, United States, 35294-0010

Sponsors and Collaborators

University of Alabama at Birmingham

Investigators

• Principal Investigator: Kent M. Daum, O.D., Ph.D.; School of Optometry, University of Alabama at Birmingham

More Information

• ClinicalTrials.gov Identifier: NCT00585026
• Other Study ID Numbers: 1-Duam
• First Posted: January 2, 2008
• Last Update Posted: June 15, 2011
• Last Verified: December 2009

Keywords provided by University of Alabama at Birmingham:

Refractive error; Asthenopia; Presbyopia; Eyeglasses; Productivity; Visual comfort; Ergonomics

Additional relevant MeSH terms:

Presbyopia; Refractive Errors; Asthenopia; Eye Diseases