Evaluation of Screening for Visual Disorders of the Old Subject in Consultation Memory

Completed

• Conditions: Visual Disorders

• Registration Number: NCT02571647
• Lead Sponsor: Nantes University Hospital

Brief Summary

Visual disorders are often overlooked in the treatment of cognitive disorders of the elderly. Yet the visual deficit impacts the quality of life, the evolution of the autonomy and psycho-behavioral disorders in cognitive diseases. The main objective of the study is to evaluate the prevalence of visual disorders among elderly patients at consultant outpatient center of Nantes clinical gerontology as part of the consultation geriatric memory. Secondary objectives are to describe ophthalmological diseases detected and taken into the proposed ophthalmic load, to determine if there are associations between eye diseases and cognitive disorders, to estimate the proportion of patients who may have an ophthalmologic evaluation to determine the cognitive profiles and geriatric evaluation and ocular pathological, depending on the assessment of arterial stiffness. The results of this study will build a testing strategy to promote access of older patients with cognitive impairment to vision care.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2015-10-05
• Study First Submitted QC: 2015-10-06
• Study First Posted: 2015-10-08
• Study Start: 2016-01-11
• Primary Completion: 2017-04-24
• Study Completion: 2017-04-24
• Status Verified: 2019-05
• Last Update Submitted: 2019-05-09
• Last Update Posted: 2019-05-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

• Elderly over 65 years,
• Subject to consultation from memory Clinical Gerontology ambulatory center Nantes University Hospital
• Current use of spoken French
• Patient (or legal guardian, if applicable) has given its written consent
• Patient affiliated to a social security scheme

Exclusion Criteria

• Life expectancy lower 1 year
• Mobility limitation preventing the installation retinal
• Major disorders and productive behavior does not allow participation in diagnostic procedures.
• Inability to respond to instructions when performing ophthalmological examinations.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Number of participants with presence of an ophthalmological disease (symptomatic or not) after clinical evaluation.	6 month

Trial Locations

Locations (1)

Nantes University Hospital; 🇫🇷 Nantes, France