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临床试验/NCT02921087
NCT02921087已完成不适用

Connecting Contact Lenses and Digital Technology

State University of New York College of Optometry1 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2017年1月1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
23
试验地点
1
主要终点
Subjective Symptom Improvement

研究概览

简要总结

This study seeks to address whether or not different types of daily disposable soft contact lenses may be a beneficial option for patients complaining of eye strain and visual discomfort while using digital devices.

详细描述

This was a prospective, single site, randomized, double-masked, crossover pilot study. Subjects were randomized to begin with either multifocal or single vision distance contact lenses. The lenses used in this study were the 1-Day Acuvue (AV) Moist spherical single-vision soft contact lenses (SSCL) in the 8.5 base curve and the 1-Day AV Moist Multifocal (MFSCL) in the low ADD (etafilcon A, 58% water content). The preferred viewing distance on digital devices for a similar age group to our study was 63 cm which would require a near ADD of +1.59D. A low addition (ADD) yielding up to +1.25D was selected to provide an intermediate near addition without compromising distance vision as much as would be expected with higher add powers. The multifocal lens utilizes an aspheric center-near design. Subjects wore the lenses on a daily wear, daily disposable schedule. Following one week (± 2 days) of lens wear, subjects were evaluated and the alternate lenses dispensed. Adverse events were collected and assessed at each study visit.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 18 to 35 years of age
  • Spectacle prescription of -0.75 to -6.00 D sphere with no more than 0.75 diopters of refractive cylinder
  • Current single-vision soft contact lens wearer
  • Monocular acuity of 20/25 or better in each eye (Snellen)
  • Self-reported minimum of 6 hours a day on digital devices
  • Self-reported complaint of eyestrain on digital devices
  • No ocular pathology and/or history of eye surgery
  • No history of strabismus or strabismus surgery
  • No gas permeable lens wear for at least 3 months
  • Subjects may not be optometrists, opticians or optometry students

排除标准

  • Corneal staining, blepharitis and/or Meibomian Gland Dysfunction (MGD) worse than Grade 2 using the Efron Grading Scale
  • Negative Relative Accommodation (NRA) less than +1.50 D
  • Exophoria at near > 6 prism diopters10
  • Vertical phoria > 1 prism diopter
  • Presence of tropia
  • Response of 3 or higher on question 2b of the Contact Lens Dry Eye Questionnaire- 8 (CLDEQ-8)
  • Unacceptable contact lens fit (i.e. substantially decentered, excessive movement)

结局指标

主要结局

Subjective Symptom Improvement

时间窗: Baseline and after 1 week of wearing each lens.

The primary outcome measure was change in average score on a ten question Visual Comfort Survey using a Visual Analogue Scale (VAS) from baseline to day 7 in multifocal contact lenses and single vision contact lenses. The Visual Analogue Scale ranges from 0-100 (100 being the worst symptoms) for each of the ten questions. The maximum total score is 1000, the minimum total score is 0 (no symptoms).

次要结局

  • Convergence Insufficiency Symptom Survey (CISS)(1 week)
  • Lens Preference(2 weeks)
  • Contact Lens Dry Eye Questionnaire- 8 Survey (CLDEQ-8)(1 week)
  • Near Phoria at 40cm in Multifocal Contact Lens vs Single Vision Contact Lens(1 week)
  • Lag of Accommodation in Study Lenses(1 week)

研究者

发起方
State University of New York College of Optometry
申办方类型
Other
责任方
Principal Investigator
主要研究者

Danielle Iacono

Assistant Clinical Professor

State University of New York College of Optometry

研究点 (1)

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