- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00013351
Restricted Useful Field View as a Risk Factor in Older Adults
January 20, 2009 updated by: US Department of Veterans Affairs
The relationship between Useful Field of Vision (UFOV) and falls taken by the elderly will be investigated.
UFOV is a test which measures visual attention.
The test has been used in correlating the visual attention in the elderly with their driving safety record.
The test is administered using a computer and consists of three parts: a) subject views figures which appear in the center of the computer screen and identified them as quickly as possible; b)the subject has to identify figures in the center of the screen while at the same time point to another symbol which will appear in one of eight places on the outer portion of the screen; c) the third section is similar to the second except while the subject is identifying and pointing there is a background noise.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment
150
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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Georgia
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Decatur, Georgia, United States
- VAMC, Decatur
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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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Vision impaired adults at risk for falls
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
- Time Perspectives: Prospective
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- John Fryer, Ph.D. Asst. Director, Program Analysis and Review Section (PARS), Rehabilitation Research & Development Service
- Nancy Rocheleau, Program Analyst, Program Analysis and Review Section (PARS), Rehabilitation Research & Development Service
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
April 1, 1998
Study Completion (Actual)
March 1, 2001
Study Registration Dates
First Submitted
March 14, 2001
First Submitted That Met QC Criteria
March 15, 2001
First Posted (Estimate)
March 16, 2001
Study Record Updates
Last Update Posted (Estimate)
January 21, 2009
Last Update Submitted That Met QC Criteria
January 20, 2009
Last Verified
January 1, 2001
More Information
Terms related to this study
Other Study ID Numbers
- C1830R
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.