RecruitingACTRN12607000399493

A randomised controlled trial of a low vision self-management program

A randomised controlled trial of a low vision self-management program on quality of life in people with low vision.


Sponsor

Associate Professor Jill Keeffe

Enrollment

240 participants

Start Date

Mar 1, 2007

Study Type

Interventional

Conditions

Summary

Study objectives • To determine the effectiveness of the ‘Living with Low Vision’ program in improving vision-specific quality of life and emotional well-being at 4, 10 and 16 months following baseline assessment in comparison with a control group with access to usual rehabilitation services. • To explore the impact of the ‘Living with Low Vision’ program on the uptake of rehabilitation services, use of low vision aids and devices, and home modification strategies. • To explore factors are associated with beneficial outcomes.


Eligibility

Sex: Both males and femalesMin Age: 55 Yearss

Plain Language Summary

Simplified for easier understanding

This study is testing a self-management program called 'Living with Low Vision' for older adults who have low vision. Low vision is when sight is reduced enough to affect daily life but cannot be fully corrected with glasses or surgery. The program aims to help people with low vision adapt to their condition, feel better emotionally, and stay as independent as possible. Participants will be compared to a group receiving usual rehabilitation services to see whether the program makes a measurable difference in quality of life and wellbeing. You may be eligible if: - You are 55 years of age or older - You are a client of Vision Australia and have had a low vision assessment in the last 12 months - Your vision in your better eye is below 6/12 but better than 6/480 with your usual glasses - You are living independently (not in a nursing home) - You speak English - You do not have significant cognitive impairment - You can hear well enough to follow a normal conversation You may NOT be eligible if: - There are no specific exclusion criteria for this study Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Participants are randomised to receive either the new low vision self-management program “Living with Low Vision” or continued access to usual low vision rehabilitation services. The “Living with

Participants are randomised to receive either the new low vision self-management program “Living with Low Vision” or continued access to usual low vision rehabilitation services. The “Living with Low Vision” program has been developed specifically for this study. It consists of eight 3-hour weekly facilitated group sessions. The program is structured and a facilitator manual clearly outlines the content and delivery. As well as providing information, the topics in the program are covered by exploring participants’ experiences, difficulties and solutions. Participants are encouraged to draw on their extensive life experience and coping mechanisms and to develop new skills and strategies and apply these new techniques in their daily life. Participants are given the option to bring a relative, friend or carer to the program with them.


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ACTRN12607000399493