RECRUITING

Inherited Retinal Degenerative Disease Registry

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 My Retina Tracker® Registry is sponsored by the Foundation Fighting Blindness and is for people affected by one of the rare inherited retinal degenerative diseases studied by the Foundation. It is a patient-initiated registry accessible via a secure on-line portal at www.MyRetinaTracker.org. Affected individuals who register are guided to create a profile that captures their perspective on their retinal disease and its progress; family history; genetic testing results; preventive measures; general health and interest in participation in research studies. The participants may also choose to ask their clinician to add clinical measurements and results at each clinical visit. Participants are urged to update the information regularly to create longitudinal records of their disease, from their own perspective, and their clinical progress. The overall goals of the Registry are: to better understand the diversity within the inherited retinal degenerative diseases; to understand the prevalence of the different diseases and gene variants; to assist in the establishment of genotype-phenotype relationships; to help understand the natural history of the diseases; to help accelerate research and development of clinical trials for treatments; and to provide a tool to investigators that can assist with recruitment for research studies and clinical trials.

Official Title

Foundation Fighting Blindness My Retina Tracker Registry

Quick Facts

Study Start:2014-06
Study Completion:2037-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT02435940

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Diagnosed with an inherited retinal degenerative disease OR
  1. * Glaucoma only
  2. * Diabetic retinopathy only
  3. * Non-retinal disease
  4. * Not heritable retinal disease

Contacts and Locations

Study Contact

Registry Coordinator
CONTACT
800-683-5555
Coordinator@MyRetinaTracker.org

Principal Investigator

Todd Durham, PhD
PRINCIPAL_INVESTIGATOR
Vice President, Clinical and Outcomes Research

Study Locations (Sites)

Foundation Fighting Blindness
Columbia, Maryland, 21045
United States

Collaborators and Investigators

Sponsor: Foundation Fighting Blindness

  • Todd Durham, PhD, PRINCIPAL_INVESTIGATOR, Vice President, Clinical and Outcomes Research

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 Date2014-06
Study Completion Date2037-06

Study Record Updates

Study Start Date2014-06
Study Completion Date2037-06

Terms related to this study

Keywords Provided by Researchers

  • inherited retinal degenerative disease
  • retinitis pigmentosa
  • Usher
  • Leber
  • Bardet-Biedl
  • Batten
  • Best
  • cone dystrophy
  • cone-rod dystrophy
  • choroideremia
  • congenital night blindness
  • enhanced s-cone
  • cone monochromacy
  • Goldmann-Favre
  • Kearns-Sayre
  • Refsum
  • retinoschisis
  • rod-cone dystrophy
  • rod dystrophy
  • rod monochromacy
  • Sorsby pseudoinflammatory dystrophy
  • stargardt
  • achromatopsia
  • juvenile inherited macular degeneration
  • cone dichromacy
  • cone trichromacy
  • Charcot-Marie-Tooth
  • albipunctate dystrophy

Additional Relevant MeSH Terms

  • Eye Diseases Hereditary
  • Retinal Disease
  • Achromatopsia
  • Bardet-Biedl Syndrome
  • Bassen-Kornzweig Syndrome
  • Batten Disease
  • Best Disease
  • Choroidal Dystrophy
  • Choroideremia
  • Cone Dystrophy
  • Cone-Rod Dystrophy
  • Congenital Stationary Night Blindness
  • Enhanced S-Cone Syndrome
  • Fundus Albipunctatus
  • Goldmann-Favre Syndrome
  • Gyrate Atrophy
  • Juvenile Macular Degeneration
  • Kearns-Sayre Syndrome
  • Leber Congenital Amaurosis
  • Refsum Syndrome
  • Retinitis Pigmentosa
  • Retinitis Punctata Albescens
  • Retinoschisis
  • Rod-Cone Dystrophy
  • Rod Dystrophy
  • Rod Monochromacy
  • Stargardt Disease
  • Usher Syndrome