RECRUITING

Objectively Diagnose and Monitor Treatment of Light Sensitivity

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 provide a new framework for diagnosing and monitoring treatment of light sensitivity and headache by objective measurement of facial features, pupil responses, retinal electrical responses and autonomic nerve responses to light.

Official Title

Use of Facial Feature to Objectively Diagnose and Monitor Treatment of Light Sensitivity

Quick Facts

Study Start:2019-07-11
Study Completion:2028-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03694626

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 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Julie Nellis, BSN
CONTACT
319-356-2780
julie-nellis@uiowa.edu
Jan Full, BSN
CONTACT
3193562780
jan-full@uiowa.edu

Study Locations (Sites)

University of Iowa Health Care
Iowa City, Iowa, 52242
United States

Collaborators and Investigators

Sponsor: Randy Kardon

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 Date2019-07-11
Study Completion Date2028-01-01

Study Record Updates

Study Start Date2019-07-11
Study Completion Date2028-01-01

Terms related to this study

Additional Relevant MeSH Terms

  • Photophobia
  • Traumatic Brain Injury
  • Migraine