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临床试验/NCT03305484
NCT03305484已完成不适用

Contact Lens Assessment in Youth - Soft Contacts Observation of Risk and Education (CLAY-SCORE)

Southern California College of Optometry at Marshall B. Ketchum University5 个研究点 分布在 2 个国家目标入组 171 人开始时间: 2017年12月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
171
试验地点
5
主要终点
Validation of the Contact Lens Risk Survey (CLRS)

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 39 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Validation of the Contact Lens Risk Survey (CLRS)

时间窗: twelve months

This study will further validate the CORS and facilitate its translation into clinical practice. A scoring algorithm will be developed.

Targeted Patient Education

时间窗: twelve months

Scripted patient education will be generated based on the results of the Contact Lens Risk Survey (CLRS) to determine if changes in behavior at the one and six month time point

次要结局

未报告次要终点

研究者

发起方
Southern California College of Optometry at Marshall B. Ketchum University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dawn Lam, MSc, OD

Associate Professor

Southern California College of Optometry at Marshall B. Ketchum University

研究点 (5)

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