Accommodation Disorders

NCT ID: NCT01329848

Last Updated: 2015-01-05

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

83 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-12-31

Study Completion Date

2013-08-31

Brief Summary

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This project will develop clinically useful, objective measurements of accommodative insufficiency and fatigue using continuous autorefraction recordings. The development of these procedures will help vision care professionals diagnose and treat accommodative anomalies.

Detailed Description

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This project studies accommodative function, the ability to focus while doing near work. Visual discomfort symptoms, such as headaches, sore eyes, and blurred vision are commonly associated with prolonged reading or other near work. Researchers have long suspected accommodative dysfunction was involved but most clinical studies have failed to establish a relationship between weak accommodation and symptoms or reading impairments. Recent research, however, has found that clinical measure overestimate accommodative function and encourage the use of objective, autorefraction methods to measure and study accommodative weakness. This project will accomplish three goals. First, using autorefraction objective reliable procedures will be developed for measuring accommodative lag, the difference between the target location and where the eye is focused. Second, experiments will measure in real-time the impact of accommodative lag on reading fluency and visual discomfort systems. Third, studies will explore the role of the slow adaptive component in accommodative weakness. This work will lead to better methods for diagnosing and treating accommodative disorders.

Conditions

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Accommodative Insufficiency Ill-sustained Accommodation

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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discomfort symptoms

level of discomfort symptoms while performing near work

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* older adolescent and young adult
* skilled readers who attend school
* are skilled readers
* have heavy reading demands

Exclusion Criteria

* Age \> 30.
* Abnormal vergence system.
* Dry-eye.
* Uncorrected visual defects or significant ocular pathology.
* Learning disability or low IQ
* Medical conditions that might cause uncomfortable visual symptoms (e.g., migraine headaches, epilepsy, head trauma); sensory defects (e.g., deafness), or neurological conditions (e.g., stuttering) that could impair reading development or oral reading fluency.
* Somatosensory amplification.
* Systemic illness or medication associated with accommodative dysfunction.
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Southern California College of Optometry at Marshall B. Ketchum University

OTHER

Sponsor Role collaborator

Western University of Health Sciences

OTHER

Sponsor Role lead

Responsible Party

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Christopher Chase

Professor of Optometry

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Chris Chase, PhD

Role: PRINCIPAL_INVESTIGATOR

Western University of Health Sciences

Locations

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Western University of Health Sciences

Pomona, California, United States

Site Status

Countries

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United States

Other Identifiers

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1R15EY021021

Identifier Type: NIH

Identifier Source: org_study_id

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