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Vision, Low clinical trials

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NCT ID: NCT00946062 Completed - Aged Clinical Trials

Evaluation of a Standardised Orientation and Mobility Training in Older Adults With Low Vision

Start date: November 2007
Phase: N/A
Study type: Interventional

The purpose of this study is: 1. to develop a standardised orientation and mobility training (O&M-training) in the use of an identification/symbol cane by older adults with low vision, and; 2. to evaluate this newly developed standardised O&M-training with respect to effectiveness and feasibility in a randomised controlled trial.

NCT ID: NCT00545220 Completed - Low Vision Clinical Trials

Problem Solving Training and Low Vision Rehabilitation

Start date: October 2007
Phase: N/A
Study type: Interventional

Vision loss can result in feelings of frustration, helplessness, anxiety, depression, and anger, which compromise a person's activities of everyday living. While emotional distress may resolve in some persons without intervention, unmanaged and persistent distress places the person at risk for continued decrements in health status and the potential development of more severe conditions (i.e., depression, poor health outcomes). Persons with low vision will be recruited and randomly assigned to either an innovative, problem-solving training (PST) intervention group designed specifically for persons with low vision or a sham intervention/control group. Primary and secondary outcomes will be assessed at baseline prior to intervention and at 3 month follow-up, 7 month follow-up, 12 month follow-up, and 24 month follow-up by a research interviewer masked to participants' randomization. This project will: (1) demonstrate how specified physical and emotional outcomes of persons with low vision change across time, (2) evaluate the effectiveness of a PST intervention that will be delivered to persons with low vision; and (3) identify persons with low vision who are at risk for adverse emotional and health outcomes.

NCT ID: NCT00366392 Completed - Vision, Low Clinical Trials

Project Magnify - A Comparison of Two Strategies to Improve Reading Ability

Start date: May 2005
Phase: Phase 4
Study type: Interventional

The purpose of Project Magnify is to determine which of the two current strategies (large print versus optical aids) for helping visually impaired students improve their reading abilities works better. Our hypothesis is that optical aids work better than providing the student with large print materials. Since large print materials are of one size only, and the level of visual impairments among students varies greatly, it seems apparent that large print materials will work well for some students, but not for all. An optical aid designed for each individual student's level of impairment seems to hold more promise in helping each student reach their maximum level of performance. Although Project Magnify is designed to increase reading abilities, it is expected that students will also develop greater independence and confidence in home and community activities that require the use of vision.

NCT ID: NCT00348621 Completed - Cataract Clinical Trials

A Study of Interventions to Reduce Disability From Visual Loss in Nursing Home Residents

Start date: June 1999
Phase: Phase 4
Study type: Interventional

The purpose of this clinical trial is to determine if interventions within the nursing home to restore vision, or cope with visual loss, in residents with visual impairment result in improvement or less decline in mobility scores, and socialization scores, compared to residents with visual impairment in nursing homes with no such intervention. The investigators hypothesized that nursing home residents with visual loss who receive cataract surgery, or refractive correction, or low vision aids would have have better socialization scores and mobility scores at 6 months and 12 months compared to nursing home residents with visual impairment who are advised to seek services, but have no specific program.

NCT ID: NCT00223756 Completed - Vision, Low Clinical Trials

VA Low Vision Intervention Trial

LOVIT
Start date: November 2004
Phase: N/A
Study type: Interventional

The primary purpose of this research study is to evaluate the effectiveness of a new outpatient low vision rehabilitation program that is targeted to serve legally blind veterans with central vision loss. The hypothesis is that veterans in the treatment group will self-report less difficulty performing daily activities than veterans in the control group who are on a waiting list for VA low vision or blind rehabilitation programs.

NCT ID: NCT00219427 Completed - Vision, Low Clinical Trials

Retina Projection System Trials for Low Vision People

Start date: January 2005
Phase: N/A
Study type: Observational

1. Purpose a. Examination on Efficacy of Retina Projection System 2. Patients a. Low vision patients 3. Methods 1. Vision aids - Retina Projection System - Face-mounted video display as control 2. Comparison of Reading Speeds with both vision aids

NCT ID: NCT00013377 Completed - Low Vision Clinical Trials

Predictors of Driving Performance and Successful Mobility - Rehabilitation in Patients With Medical Eye Condition

Start date: April 1999
Phase: Phase 2
Study type: Interventional

There are two diseases in particular that may have serious consequences for driving and mobility due to their potentially severe impact on visual function: glaucoma and diabetic neuropathy. In this project we will develop predictive models of driving for these patients and will train them to use low-vision aids to improve driving mobility. We will determine how best to train patients with hemianopic field loss due to cerebral vascular accidents and identify predictors of long-term success in the use of low-vision aids.

NCT ID: NCT00001346 Completed - Clinical trials for Diabetic Retinopathy

Diabetic Retinopathy and Visual Function Study

Start date: November 1992
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate possible mechanisms of central visual loss in patients with diabetes mellitus. The visual loss of interest to be investigated is that associated with macular edema (prior to and following laser photocoagulation treatment) and that associated with panretinal photocoagulation. The evaluation will be performed with psychophysical testing, i.e., static perimetry and contrast sensitivity function. Of particular interest, the mechanisms of visual loss associated with macular edema (prior to and following laser photocoagulation) will be further investigated. Photoreceptor-mediated visual loss will be assessed by measurements of the Stiles-Crawford effect. Visual loss mediated by post-receptoral retinal changes will be assessed by measuring the Westheimer spatial desensitization/sensitization effect.