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Telerehabilitation for Visually Impaired

Usability and Adherence of Visually Impaired to Telerehabilitation: a Multicentre Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05772793
Enrollment
50
Registered
2023-03-16
Start date
2021-07-07
Completion date
2022-01-27
Last updated
2023-03-16

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

Conditions

Visual Impairment

Brief summary

the purpose of the study is to evaluate the software usability and patient's adherence from five vision rehabilitation centres. In addition, the effect and benefits of a customizable telerehabilitation program were tested.

Detailed description

The software is used in our practice for every day vision rehabilitation training. So it is part of our routine medical care, and a we are going to study studies the effect of the intervention in several different centers.

Interventions

DEVICETelerehabilitation

The home visual telerehabilitation path using the EyeFitness software consisted of performing one visual training session per day, 5 days a week (from Monday to Friday) for a total of 6 weeks.

Sponsors

Amore Filippo
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years

Inclusion criteria

* All patients were eligible if they were over 18 years old and had a best corrected visual acuity (BCVA) between 1.3 logMAR and 0.4 LogMAR and/or a visual field of less than 60%, according to the WHO classification.

Exclusion criteria

* Subjects were excluded if they had a cognitive/psychiatric impairment or a motor disability that prevents the use of a computer pointing device (mouse).

Design outcomes

Primary

MeasureTime frameDescription
Utility of EyeFitness telerehabilitation6 monthsThe aim of this study is to evaluate the utility of the EyeFitness telerehabilitation software and the adherence of patients to the treatment. In order to evaluate the utility of the software the primary outcome measures were PSSUQ Version 3 scores defined as Overall, System Usefulness (Sysuse), Information Quality (Infoqual), Interface Quality (Iterqual).

Secondary

MeasureTime frameDescription
Effect of treatment6 monthsThe secondary outcome measures selected for the effectiveness analysis were distance Best Corrected Visual Acuity, MNRead reading acuity, reading speed (words per minute), contrast sensitivity (at Pelli - Robson charts) and fixation stability according to Microperimeter exame classification.

Countries

Italy

Outcome results

None listed

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