Refraction Determination Analysis

NCT01995435 — Not applicable, Completed, 30 participants, Lee, Steven, M.D.

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RegistryNCT01995435
StatusCompleted
PhaseNot applicable
Study typeInterventional; randomized, crossover, masking: triple, diagnostic
Enrollment30 (Actual)
SponsorLee, Steven, M.D. (Indiv)
ConditionsMyopia,, Hyperopia,, Astigmatism,, Presbyopia,, Eye Strain,
InterventionsTelemedicine refraction, Traditional refraction (Device)
Datesstart 2015-02-01, primary completion 2015-06-01, completion 2015-06-01, first posted 2013-11-26, last updated 2015-09-07

Related Papers Related Patents Related Grants Related Experts
All trials for Myopia, All trials for Hyperopia, All trials of Telemedicine refraction All trials of Traditional refraction

-Summary

Correlating the accuracy of a refraction done over telemedicine to that of a standard refraction, with a study hypothesis that the results will be equivalent.

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+Arms and interventions

ArmTypeInterventionsDescription
Telemedicine refraction before traditional refractionExperimentalDevice: Telemedicine refraction; Device: Traditional refractionWe will first refract an individual using telemedicine refraction, and then refract them using a traditional refraction method.
Traditional refraction before telemedicine refractionExperimentalDevice: Telemedicine refraction; Device: Traditional refractionWe will first refract an individual using a traditional refraction, and then refract them using a telemedicine refraction method.
  • Telemedicine refraction (Device), also known as Glasses,, Contact lenses,, Refractive surgery,
  • Traditional refraction (Device)

+Outcome measures

Primary outcomes

  • refraction in diopters over telemedicine compared standard phoropter refraction [an average of 1 year]

Secondary outcomes

  • telemedicine refraction results beyond dioptric readings [an average of 1 year]: to see if there are other uses for telemedicine refraction results

Other outcomes

  • patient satisfaction from telerefraction [an average of 1 year]

+Eligibility

Sex: All, ages: 18 Years to 40 Years, accepts healthy volunteers

Inclusion Criteria:

* 18-40 years old
* healthy eyes

Exclusion Criteria:

* mid level ocular diseases (glaucoma, hypertension, retinal issues)
* psychiatric disorders
* brain tumor or history of
* under 18, or over 40 years old