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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02571647
Acronym
EVAM
Enrollment
300
Registered
2015-10-08
Start date
2016-01-11
Completion date
2017-04-24
Last updated
2019-05-10

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

Conditions

Visual Disorders

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.

Interventions

OTHERNon interventional study

Patients agreeing to participate in the study will have a cognitive assessment and geriatric assessment, carried out according to usual practices and grids clinical gerontology cluster. They will benefit in addition to a noninvasive screening and risk-free ophthalmic (visual acuity, intraocular pressure, examination of the eyelids and fundus).

Sponsors

Nantes University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Number of participants with presence of an ophthalmological disease (symptomatic or not) after clinical evaluation.6 month

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026