Soft Contacts Observation of Risk and Education (SCORE)
Status: | Not yet recruiting |
---|---|
Healthy: | No |
Age Range: | 18 - 39 |
Updated: | 10/12/2017 |
Start Date: | October 2017 |
End Date: | September 2018 |
Contact: | Dawn Lam, OD |
Email: | dlam@ketchum.edu |
Phone: | 7145018879 |
Contact Lens Assessment in Youth - Soft Contacts Observation of Risk and Education (CLAY-SCORE)
Specific Aims
1. Develop risk assessment scores for SCL wearers
2. Test the scoring algorithm in SCL wearers who present with adverse events
3. Explore targeted patient education to reduce risk behaviors associated with SCL wear.
1. Develop risk assessment scores for SCL wearers
2. Test the scoring algorithm in SCL wearers who present with adverse events
3. Explore targeted patient education to reduce risk behaviors associated with SCL wear.
This will be a multi-center, case-control prospective study. Subjects will be enrolled at
five geographically diverse locations across North America. The intent is to enroll cases
with new (untreated) red eyes and controls that are representative of the contact lens
wearing population and test the new scoring algorithm on this population.
A total of 232 participants are expected to complete the study (116 case-control sets).
Enrollment will be competitive. After consent, subjects will complete the Contact Lens Risk
Survey (CLRS) online at www.claystudy.org. Data related to symptoms, medical history and
anterior segment evaluation will be collected. Subjects will be treated as usual and
customary by the investigator. No intervention of treatment in this study. Subjects will be
asked to repeat the CLRS at one and six months post initial visit.
Initial factor analysis from the previous CLRS data were used to develop and test the CLRS
algorithm. Five sub-scales were identified in the areas of contact lens care, contact lens
dependence, hygiene, living arrangements and wellness. Assuming a 10% missing data rate, a
total of 58 SCL wearers with "serious and significant" red eye events will allow for
detection of 0.4 or larger effect size.
There are multiple steps to "compliant wear" of contact lenses and while many patients do
many of the correct wear behaviors, it's not realistic for practitioners to re-educate all
wearers on all of the steps necessary to successfully wear SCLs. The CLRS allows patients to
quickly report their specific wear behaviors and then receive only the targeted information
on which behaviors they are doing that puts them at higher risk. A previous CLAY study
demonstrated good repeatability of the CLRS survey one week after initial fielding.
five geographically diverse locations across North America. The intent is to enroll cases
with new (untreated) red eyes and controls that are representative of the contact lens
wearing population and test the new scoring algorithm on this population.
A total of 232 participants are expected to complete the study (116 case-control sets).
Enrollment will be competitive. After consent, subjects will complete the Contact Lens Risk
Survey (CLRS) online at www.claystudy.org. Data related to symptoms, medical history and
anterior segment evaluation will be collected. Subjects will be treated as usual and
customary by the investigator. No intervention of treatment in this study. Subjects will be
asked to repeat the CLRS at one and six months post initial visit.
Initial factor analysis from the previous CLRS data were used to develop and test the CLRS
algorithm. Five sub-scales were identified in the areas of contact lens care, contact lens
dependence, hygiene, living arrangements and wellness. Assuming a 10% missing data rate, a
total of 58 SCL wearers with "serious and significant" red eye events will allow for
detection of 0.4 or larger effect size.
There are multiple steps to "compliant wear" of contact lenses and while many patients do
many of the correct wear behaviors, it's not realistic for practitioners to re-educate all
wearers on all of the steps necessary to successfully wear SCLs. The CLRS allows patients to
quickly report their specific wear behaviors and then receive only the targeted information
on which behaviors they are doing that puts them at higher risk. A previous CLAY study
demonstrated good repeatability of the CLRS survey one week after initial fielding.
Inclusion Criteria:
- CASES
- Current SCL wear (as defined by having worn lenses in previous week) without
restriction on lens material, design, indication, wearing schedule or lens power
- 18 - 39 years of age
- New (untreated) symptomatic red eye CONTROLS
- Current SCL wear (as defined by having worn lenses in previous week) without
restriction on lens material, design, indication, wearing schedule or lens power
- 18 - 39 years of age and gender and age-matched (± 3 years) to Case
- Have not had an eye care examination within the past three months
Exclusion Criteria:
- CASES
- Faculty, staff or student at an optometry college or school
- Family or household member of an eye care provider, ophthalmic technician,
ophthalmology or optometry residents or optometry students
- Pregnancy (by self-report)
- Currently enrolled in another eye/vision clinical trial
- Previous participant in a CLAY study
- Wearing SCL in conjunction with gas permeable (GP) lenses (i.e., piggyback
design, hybrid lens.) CONTROLS
- Same exclusion criteria as cases
We found this trial at
5
sites
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4901 Calhoun Road
Houston, Texas 77204
Houston, Texas 77204
Principal Investigator: Kathryn Richdale, OD
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338 West 10th Avenue
Columbus, Ohio 43210
Columbus, Ohio 43210
Principal Investigator: Aaron Zimmerman, OD
Phone: 614-292-4196
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Fort Lauderdale, Florida 33328
Principal Investigator: Chandra Mickles, OD
Phone: 908-675-1543
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200 Columbia Street West
Waterloo, Ontario N2L 3G1
Waterloo, Ontario N2L 3G1
Principal Investigator: Luigina Sorbara, OD
Phone: 905-702-2451
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