Clinical Effectiveness of Low Vision Rehabilitation in Glaucoma Patients (LOVIT)
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|ClinicalTrials.gov Identifier: NCT01262209|
Recruitment Status : Completed
First Posted : December 17, 2010
Last Update Posted : September 9, 2016
Our team is interested in what can be done to improve the functioning of patients who suffer from glaucoma, a chronic and irreversible eye disease. Patients with vision loss as a result of this disease may feel like they have been 'given up on', or lost to our medical system when no further interventions can be offered to treat their eye disease. It is our intent to investigate what alternatives we can provide our patients, instead of simply saying, 'nothing more can be done'. We have learned from studies done on other chronic eye diseases, like age related macular degeneration, that low vision rehabilitation can improve visual function.
What exactly is low vision? It can involve a loss of visual acuity, making activities such as reading or writing a challenge; it can involve loss of contrast sensitivity, making shapes and edges hard to discern, like those of a stair edge, or person's face. It could also involve a loss of peripheral, or side vision which is a symptom common to most glaucoma patients. Whatever the cause of low vision, doing day-to-day activities can become increasingly difficult, and many suffer from a loss of their independence and may even become depressed. Low vision rehabilitation involves helping patients to use their remaining vision in optimal, and sometimes even new, ways. This involves an assessment of a person's baseline vision, and an idea of what their needs are. Patients are then given low vision aids (such as magnifiers, telescopes, video screens which magnify images, and other tools) as well as instructions and support for adapting to living and functioning with altered vision.
Although there currently exists no cure for glaucoma, and we are certainly not promising a reversal of the damage done to the eyes from this chronic disease, we do believe that these types of rehabilitation services may offer some hope and potential visual benefit to patients living with vision loss. Our hypothesis is that the use of state-of-the-art low vision aids in patients with advanced glaucomatous visual loss will provide an improvement in visual tasks and thereby an improvement in quality of life.
|Condition or disease||Intervention/treatment||Phase|
|Glaucoma||Device: portable CCTV Device: Telescopes, telemicroscopes and microscopes Device: Absorptive filters||Not Applicable|
Show Detailed Description
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||16 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Supportive Care|
|Official Title:||Clinical Effectiveness of Low Vision Rehabilitation in Glaucoma Patients With Moderate or Severe Vision Loss|
|Study Start Date :||May 2011|
|Actual Primary Completion Date :||April 2015|
|Actual Study Completion Date :||August 2015|
Experimental: Low Vision Aids
All patients will receive:
Device: portable CCTV
This is a small handheld mini screen intended to improve reading.Device: Telescopes, telemicroscopes and microscopes
These are either worn like glasses, or held in one's hand and are intended to improve distance vision (like details of a hockey game), intermediate vision (like reading a sign), or 'up-close' vision (like reading small print).Device: Absorptive filters
These are worn like glasses, and have tinted colour lenses. They are intended to improve contrast sensitivity, or being able to tell light from dark (like reading gray letters on a white background).
- Visual reading ability and visual mobility. [ Time Frame: 2 weeks ]The primary outcome measure will be visual reading ability and visual mobility.
- Other visual ability domains. [ Time Frame: 2 weeks ]Mean changes in other visual ability domains (overall ability, visual information processing and visual motor skills) on the VA LV VFQ-48 from baseline to two weeks are the secondary outcome measures.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01262209
|Ivey Eye Institute|
|London, Ontario, Canada, N6A 4V2|
|Principal Investigator:||Cindy ML Hutnik, Bsc(Hon), MD, PhD, FRCSC||Ivey Eye Institute|