Refraction Determination Analysis

NCT ID: NCT01995435

Last Updated: 2015-09-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-02-28

Study Completion Date

2015-06-30

Brief Summary

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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.

Detailed Description

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Conditions

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Myopia, Hyperopia, Astigmatism, Presbyopia, Eye Strain,

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Telemedicine refraction before traditional refraction

We will first refract an individual using telemedicine refraction, and then refract them using a traditional refraction method.

Group Type EXPERIMENTAL

Telemedicine refraction

Intervention Type DEVICE

Traditional refraction

Intervention Type DEVICE

Traditional refraction before telemedicine refraction

We will first refract an individual using a traditional refraction, and then refract them using a telemedicine refraction method.

Group Type EXPERIMENTAL

Telemedicine refraction

Intervention Type DEVICE

Traditional refraction

Intervention Type DEVICE

Interventions

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Telemedicine refraction

Intervention Type DEVICE

Traditional refraction

Intervention Type DEVICE

Other Intervention Names

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Glasses, Contact lenses, Refractive surgery,

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Lee, Steven, M.D.

INDIV

Sponsor Role lead

Responsible Party

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Coad Dow, MD

Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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SPL-321-REF

Identifier Type: -

Identifier Source: org_study_id

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