- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00341744
Providing Access to the Visual Environment
Study Overview
Status
Conditions
Detailed Description
Subjects are enrolled each school year based on referrals from school systems in Tennessee, ophthalmologists, and optometrists. A total of 90 new students are enrolled each year. Students are provided a comprehensive low vision rehabilitation evaluation by a low vision optometrist and prescribed optical devices to improve distance appreciation, near reading, and other tasks based on individual needs. Students are then trained to use the devices efficiently by master's level teachers of the visually impaired. The teachers travel to the students environment (school/home/work) for the training.
Variables such as ocular disease, age, visual acuity, visual improvement with optical devices, type of optical device, and reading speed are defined for each student. Providing Access to the Visual Environment also provides...
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Lori Ann F Kehler, O.D.
- Phone Number: 615-936-2020
- Email: lori.ann.kehler@Vanderbilt.Edu
Study Contact Backup
- Name: Saige Wilkins, CTS
- Phone Number: 615-936-1474
- Email: saige.wilkins@vumc.org
Study Locations
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Tennessee
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Nashville, Tennessee, United States, 37232
- Recruiting
- Saige Wilkins
-
Contact:
- Saige A Wilkins, CTS
- Phone Number: 615-936-1474
- Email: saige.wilkins@vumc.org
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Contact:
- Lori Ann Kehler, O.D.
- Phone Number: 615-936-2020
- Email: lori.ann.kehler@Vanderbilt.Edu
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Principal Investigator:
- Lori Ann Kehler, O.D
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
Children age 3 to 21 years of age Enrollment in a school in Tennessee (private or public)
- Children that are eligible for services due to visual impairment Low vision
Exclusion Criteria:
- Children who do not have the potential to become readers or use their vision for reading
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Success to utilize optical devices
Time Frame: 3-4 months
|
Training with external optical devices to improve visual outcome
|
3-4 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Lori Ann Kehler, O.D., Vanderbilt Eye Institute
Study record dates
Study Major Dates
Study Start
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
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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