- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01329848
Accommodation Disorders (AD)
December 23, 2014 updated by: Christopher Chase, Western University of Health Sciences
Using Accommodative Lag to Diagnose Accommodation Disorders
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.
Study Overview
Status
Completed
Detailed Description
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.
Study Type
Observational
Enrollment (Actual)
83
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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California
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Pomona, California, United States, 91766
- Western University of Health Sciences
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 30 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Graduate students from Western University of Health Sciences
Description
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.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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discomfort symptoms
level of discomfort symptoms while performing near work
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Accommodation Lag 5D
Time Frame: 3 week period
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Lag will be measured at different viewing distances and durations using autorefraction.
Accommodation error refers to the difference between the distance where the target is located and where the eyes focus.
Lag refers error that is under focussed; lead is error that is over focussed.
This distance is measured in diopters, or 1/meter.
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3 week period
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Conlon Symptom Survey
Time Frame: 3 weeks
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Measures visual discomfort symptoms while doing near work.
23 item survey using a 4-point rating scale (never, occasionally, often, almost always).
Total raw score reported on a range from 0 to 69 with higher scores indicating more frequent symptoms.
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3 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Chris Chase, PhD, Western University of Health Sciences
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2010
Primary Completion (ACTUAL)
December 1, 2012
Study Completion (ACTUAL)
August 1, 2013
Study Registration Dates
First Submitted
April 4, 2011
First Submitted That Met QC Criteria
April 4, 2011
First Posted (ESTIMATE)
April 6, 2011
Study Record Updates
Last Update Posted (ESTIMATE)
January 5, 2015
Last Update Submitted That Met QC Criteria
December 23, 2014
Last Verified
December 1, 2014
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1R15EY021021 (NIH)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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