Assessing quality of life in visually impaired patients in Italy
Observational Study on Quality of Life in Visually Impaired Patients Through the Questionnaire VA LV VFQ in Italy
Fondazione Policlinico Universitario Agostino Gemelli IRCCS · NCT05752214
This study is trying to see how visual rehabilitation affects the quality of life for adults in Italy who have vision problems.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Fondazione Policlinico Universitario Agostino Gemelli IRCCS (other) |
| Locations | 1 site (Roma) |
| Trial ID | NCT05752214 on ClinicalTrials.gov |
What this trial studies
This observational study aims to create a clinical register of visual rehabilitation activities and validate the Visual Acuity Low Vision Functional Questionnaire (VA LV VFQ) within the Italian context. It will involve patients aged 18 and older who are receiving visual rehabilitation for various visual pathologies. Participants will be asked to complete the questionnaire to assess their quality of life related to visual impairment. The study will help gather data that can improve rehabilitation services and patient care.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older with any form of visual impairment seeking rehabilitation.
Not a fit: Patients under 18 years old or those with cognitive impairments that hinder understanding of the consent process or questionnaire will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the understanding of quality of life in visually impaired patients, leading to improved rehabilitation strategies.
How similar studies have performed: While this study focuses on a specific population in Italy, similar observational studies have shown success in validating quality of life assessments for visually impaired individuals in other contexts.
Eligibility criteria
Show full inclusion / exclusion 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.
Where this trial is running
Roma
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS — Roma, Italy (RECRUITING)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Visual Impairment