RECRUITING

Smartphone Flicker Fusion Test for Patients With Optic Disorders.

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this project is to validate a quick, easy-to-use and administer smartphone flicker fusion test. The app (called eyeFusion) can potentially be used to easily and quickly collect critical flicker fusion measurements on patients admitted with optic disorders as part of the clinical care process.

Official Title

Validation of a Smartphone-Based Flicker Fusion Test

Quick Facts

Study Start:2017-01-27
Study Completion:2028-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03475147

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.

Ages Eligible for Study:18 Years to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age matched 18-80 years of age.
  2. * Healthy normal controls with no known eye disorders.
  1. * Scotoma or any other ocular disorder
  2. * Age 18-80
  3. * Clinically associated scotoma

Contacts and Locations

Study Contact

Julie K Nellis, BSN
CONTACT
319-356-2780
julie-nellis@uiowa.edu
Jan Full, BSN
CONTACT
319-356-8299
jan-full@uiowa.edu

Principal Investigator

Randy Kardon, MD, PhD
PRINCIPAL_INVESTIGATOR
University of Iowa

Study Locations (Sites)

University of Iowa
Iowa City, Iowa, 52240
United States

Collaborators and Investigators

Sponsor: Randy Kardon

  • Randy Kardon, MD, PhD, PRINCIPAL_INVESTIGATOR, University of Iowa

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 Registration Dates

Study Start Date2017-01-27
Study Completion Date2028-01-01

Study Record Updates

Study Start Date2017-01-27
Study Completion Date2028-01-01

Terms related to this study

Additional Relevant MeSH Terms

  • Scotoma