RECRUITING

Eye Movement Rehabilitation in Low Vision Patients

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

Approximately 217 million people worldwide currently suffer from low vision, which impacts a broad range of activities of daily living and is associated with depression and increased mortality. Over half of the patients presenting for low vision services have eye disease that affects the fovea and surrounding macula and leads to central vision loss (CVL). People with CVL are forced to use eccentric vision as a substitute for their impaired fovea, however eye movement control and visual function is impaired with eccentric vision. Recent evidence and preliminary results from the investigators show that rehabilitation methods can help improve oculomotor control and this can lead to improved functional outcomes. The investigators have developed new feedback-based training methods that aim to improve eccentric vision use by patients with CVL. In a series of studies, the investigators examine rehabilitation of fixation control, smooth pursuit eye movements that track moving objects and saccadic eye movements that abruptly change the point of regard. The investigators examine how visual feedback, scotoma awareness methods and hand-eye coordination can improve eccentric vision use. Improvements in oculomotor control are quantified with eye tracking methods and associated changes in visual function are quantified with acuity, contrast sensitivity and reading performance. The proposed research therefore develops and translates state-of-the-art methods in basic science to clinical applications. Accomplishing the proposed aims will provide new and improved methods for rehabilitation strategies for visual impairment. The ultimate goal of this proposal is to maximize the residual visual function of people with low vision and to help them to live independently, thereby improving quality of life and minimizing the economic and social burden of visual impairment.

Official Title

Eye Movement Rehabilitation in Low Vision Patients

Quick Facts

Study Start:2020-09-04
Study Completion:2024-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04929756

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:14 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * over 14 year of age
  2. * logMAR Acuity 0.5-1.0
  3. * Bi-lateral foveal scotomas \< 7 °radius
  4. * Mini Mental State questionnaire ≥ 29
  5. * no history of concurrent peripheral vision loss
  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

Peter J Bex, PhD
CONTACT
6173736214
p.bex@northeastern.edu
Nicole C Ross, O.D.
CONTACT
617-587-5626
rossn@neco.edu

Principal Investigator

Peter J Bex, PhD
PRINCIPAL_INVESTIGATOR
Northeastern University

Study Locations (Sites)

NECO Center for Eye Care
Boston, Massachusetts, 02215
United States
Lighthouse Guild
New York, New York, 10023
United States

Collaborators and Investigators

Sponsor: Northeastern University

  • Peter J Bex, PhD, PRINCIPAL_INVESTIGATOR, Northeastern University

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 Date2020-09-04
Study Completion Date2024-01-31

Study Record Updates

Study Start Date2020-09-04
Study Completion Date2024-01-31

Terms related to this study

Additional Relevant MeSH Terms

  • Low Vision
  • Age Related Macular Degeneration