Age-Related Macular Degeneration, Scotopic Dysfunction, and Driving Performance in a Simulator

Sponsor
University of Alabama at Birmingham (Other)
Overall Status
Completed
CT.gov ID
NCT03166202
Collaborator
(none)
40
1
6.1
6.6

Study Details

Study Description

Brief Summary

Previous work collectively suggests that rod-mediated dark adaptation (RMDA) is a promising candidate as a functional endpoint measure for evaluating interventions to slow early progression of age-related macular degeneration (AMD). However, there is no agreement among the clinical, research and regulatory communities as to what constitutes a clinically (practically) significant slowing in RMDA. Treatments for AMD are often not considered efficacious if they do not result in a criterion level of improvement in vision. But how much change in the rate of dark adaptation constitutes a clinically significant change? Until this issue is resolved, progress in developing clinical trials on early AMD are at a standstill since there is no functional endpoint to be used in the trial. One approach to establishing clinical significance is to examine how RMDA relates to the performance of an everyday visual task under low luminance conditions, such as night driving or reading. However, such data are not yet available. The purpose of this project is to examine the relationship between RMDA and night-time driving and reading under poor illumination. This information will guide the development of a definition of a clinically significant difference in RMDA that can be used in designing clinical trials on early AMD.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The specific aims of this study are as follows:

    Aim 1: To examine the association between RMDA as assessed by the rod intercept time and self reported driving difficulty and experiences during night time driving.

    Aim 2: To examine the association between RMDA as assessed by rod intercept time and reading performance as assessed by the MNREAD test administered under a low light level. Reading performance will be defined in terms of maximum reading speed, critical print size (i.e., the smallest print size that supports maximum reading speed), reading acuity (i.e., the smallest print size that can be just read) and the reading accessibility index (i.e., an individual's access to text over the range of print sizes found in everyday life).

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    40 participants
    Observational Model:
    Cohort
    Time Perspective:
    Cross-Sectional
    Official Title:
    Age-Related Macular Degeneration, Scotopic Dysfunction, and Driving Performance in a Simulator
    Actual Study Start Date :
    Sep 1, 2018
    Actual Primary Completion Date :
    Mar 5, 2019
    Actual Study Completion Date :
    Mar 5, 2019

    Outcome Measures

    Primary Outcome Measures

    1. rod intercept time [measured once (1 day)]

      rate of rod-mediated dark adaptation

    Secondary Outcome Measures

    1. severity of age-related macular degeneration [measured once (1 day)]

      defined by grading of color fundus photos

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    60 Years to 95 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • age-related macular degeneration in one or both eyes, ability to follow simple instructions, licensed to drive a vehicle, can read and speak English
    Exclusion Criteria:
    • diabetes, retinal or optic nerve conditions other than age-related macular degeneration, neurological conditions that impair vision

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Callahan Eye Hospital, UAB Dept of Ophthalmolog & Visual Sciences Birmingham Alabama United States 35294-0009

    Sponsors and Collaborators

    • University of Alabama at Birmingham

    Investigators

    • Principal Investigator: Cynthia Owsley, PhD, University of Alabama at Birmingham
    • Principal Investigator: MiYoung Kwon, PhD, University of Alabama at Birmingham

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Cynthia Owsley, Principal Investigator, University of Alabama at Birmingham
    ClinicalTrials.gov Identifier:
    NCT03166202
    Other Study ID Numbers:
    • 228382017
    First Posted:
    May 25, 2017
    Last Update Posted:
    Jun 6, 2019
    Last Verified:
    Jun 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Cynthia Owsley, Principal Investigator, University of Alabama at Birmingham
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 6, 2019