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Clinical Trials/NCT03076606
NCT03076606
Terminated
Not Applicable

Nurses Ability to Assess Visual Acuity in Geriatric Consultation

University Hospital, Caen1 site in 1 country15 target enrollmentMarch 20, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Visual Acuity
Sponsor
University Hospital, Caen
Enrollment
15
Locations
1
Primary Endpoint
visual acuity values concordance between nurses and ophthalmologist
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

Nurses participate to geriatric evaluations for falling patients. For these patients, it is recommended to evaluate,especially, visual acuity but this is not currently done because it is difficult to systematically combine with an ophthalmologic consultation.

The HAS french recommendations propose to detect visual acuity deficiency using Monoyer and Parinaud scales, without specifying the professional qualification. According to the nurse competence decree of State Graduates, "sensory disorders" screening is a "non-vulnerable" examination, and can be performed by nurses. Therefore, they can use these scales, after training.

We propose to evaluate the correlation between visual acuity scores obtained by nurses in geriatric consultations and an ophthalmologist.

This study should include 204 patients over 65 years, who have fallen at least twice in the last 12 months. These patients will benefit from an evaluation by an ophthalmologist, after the geriatric consultation.

Registry
clinicaltrials.gov
Start Date
March 20, 2017
End Date
May 4, 2020
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • at least 2 falls in the last 12 months,
  • applied in geriatric evaluation
  • talking French
  • affiliated to the social security system

Exclusion Criteria

  • not communicating
  • illiterate
  • Total blindness

Outcomes

Primary Outcomes

visual acuity values concordance between nurses and ophthalmologist

Time Frame: day 1

On 2 (near and far) binocular values per patient with their usual glasses. Concordance is assessed on the assignment of patients to one of the 3 groups: ≤ 5 / 10e, 6-7 / 10 e, ≥ 8/10 e

Secondary Outcomes

  • new diagnosis or ophthalmologic pathology aggravation(day 1)
  • cognitive influence(day 1)

Study Sites (1)

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