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Improving Vision and Quality of Life in the Nursing Home

Improving Vision and Quality of Life in the Nursing Home

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00347620
Enrollment
400
Registered
2006-07-04
Start date
2000-08-31
Completion date
2003-12-31
Last updated
2010-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract, Refractive Error

Brief summary

The primary purpose of this study is to evaluate whether interventions to improve vision in nursing home residents have an impact on residents' health-related quality of life. The interventions being evaluated are correction of refractive error (near-sightedness, far-sightedness, presbyopia) and cataract surgery.

Detailed description

The purpose of this project is two-fold: 1.) to establish the psychometric properties of the Nursing Home Vision-Specific Health-Related Quality of Life (HRQOL) instrument, and; 2.) to evaluate the responsiveness of this instrument. Responsiveness will be assessed in two independent preliminary prospective intervention evaluations. The first responsiveness evaluation will involve a new spectacle intervention and the second will involve first eye cataract surgery. In addition, we will examine the association between the responsiveness of this instrument, and changes in visual functioning measures and other demographic variables.

Interventions

DEVICEspectacles
PROCEDURECataract Surgery

Sponsors

Retirement Research Foundation
CollaboratorOTHER
National Institute on Aging (NIA)
CollaboratorNIH
National Eye Institute (NEI)
CollaboratorNIH
Research to Prevent Blindness
CollaboratorOTHER
EyeSight Foundation of Alabama
CollaboratorOTHER
Pearle Vision Foundation
CollaboratorUNKNOWN
University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* at least 60 years of age or older * expected to stay in facility foe at least 8 months * stable medical condition * moderately cognitively impaired or better

Exclusion criteria

* those not meeting inclusion criteria

Design outcomes

Primary

MeasureTime frame
vision-targeted health-related quality of life

Secondary

MeasureTime frame
generic health-related quality of life
functional independence
participation in group activities
depression
falls
life space
physical activities

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 6, 2026