Clinical Assessment of a Customized Free-form Progressive Addition Lens Spectacle
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 39 - 80 |
Updated: | 4/19/2017 |
Start Date: | February 2009 |
End Date: | October 2009 |
The purpose of this study was to compare objective clinical measures of visual performance
and subjective measures of satisfaction and preference between standard progressive addition
lens (PAL) spectacles and a new type of free-form surfaced, optically customized PAL
spectacle.
and subjective measures of satisfaction and preference between standard progressive addition
lens (PAL) spectacles and a new type of free-form surfaced, optically customized PAL
spectacle.
In a double-masked crossover trial, 95 experienced wearers wore customized free-form PAL
spectacles (Test) and standard non-free-form PAL spectacles (Control) for one week each. All
subjects wore both Test and Control spectacles, and the pair to be worn first was randomly
assigned. At dispensing and after 1 week of wear, subjects were tested for distance and near
visual acuity (VA) under both high and low contrast; in addition, 30 degree off-axis VA was
measured using a novel apparatus, as was the horizontal extent of undistorted vision at
reading distance. Subjects also completed a set of questionnaires detailing their
satisfaction levels, adaptation times, and preferences for Test or Control spectacles for
different visual tasks.
spectacles (Test) and standard non-free-form PAL spectacles (Control) for one week each. All
subjects wore both Test and Control spectacles, and the pair to be worn first was randomly
assigned. At dispensing and after 1 week of wear, subjects were tested for distance and near
visual acuity (VA) under both high and low contrast; in addition, 30 degree off-axis VA was
measured using a novel apparatus, as was the horizontal extent of undistorted vision at
reading distance. Subjects also completed a set of questionnaires detailing their
satisfaction levels, adaptation times, and preferences for Test or Control spectacles for
different visual tasks.
Inclusion Criteria:
- Presbyope
- Experienced PAL spectacle wearer
- Correctable to at least 20/25 in both eyes
- Able and willing to use Test and Control spectacles for 1 week each as primary form
of presbyopia correction
- Able and willing to complete all laboratory measurements and questionnaire batteries
Exclusion Criteria:
- Purchasing free-form PAL spectacles from the UC Berkeley Eyewear Center
- Having eye conditions or diseases that could potentially cause a decrease in visual
acuity over the course of participation in the study
- Having eye conditions or diseases that could potentially interfere with ability to
use Test and Control spectacles as primary form of presbyopia correction
We found this trial at
1
site
380 Minor Lane
Berkeley, California 94720
Berkeley, California 94720
Click here to add this to my saved trials