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Recruiting NCT05752214

Quality of Life in Italian Visually Impaired Patients

Observational Visual Impairment

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: WEB Register.
Who it may be relevant to
Registry conditions: Visual Impairment. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Observational Study on Quality of Life in Visually Impaired Patients Through the Questionnaire VA LV VFQ in Italy

Overview

Clinical register of visual rehabilitation activity and observational study on the validation of the VA LV VFQ questionnaire in the Italian context

Interventions

  • Other WEB Register
    Observational, non-profit, multicentre longitudinal study on the assessment of quality of life and its association with demographic variables and visual function of visually impaired patients attending the visual rehabilitation service.

Primary outcome measures

  • VA-LV-VFQ-48 questionnaire score [Time frame: 10 years]

Eligibility criteria

Inclusion criteria

  • Subjects aged 18 years or older, suffering from any visual pathology, who are admitted to specialised visual rehabilitation centres for visual rehabilitation.
  • Ability to understand and sign the informed consent for participation in the study.

Exclusion criteria

  • Less than 18 years of age.
  • Cognitive impairment that, in the opinion of the investigator, limits understanding of the informed consent or the questionnaire.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Italy · 1 center
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS — Roma

Identifiers

NCT: NCT05752214 · 3904

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗