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Evaluation of an Updated Version of the Program BlinkBlink for Alleviation of Dry Eye Symptoms Induced by Computer Work

Evaluation of an Updated Version of the Program BlinkBlink for Alleviation of Dry Eye Symptoms Induced by Computer Work

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04637516
Enrollment
30
Registered
2020-11-19
Start date
2018-04-01
Completion date
2018-08-17
Last updated
2020-11-19

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

Conditions

Computer Vision Syndrome, Dry Eye Syndromes

Keywords

dry eye disease, computer work, computer vision syndrome

Brief summary

The program BlinkBlink was developed to alleviate dry eye symptoms during prolonged computer work. This study aimed to show subjective and objective improvement of dry eye problems in a sample size of office workers

Detailed description

The increased use of digital devices and the resulting increase in near work has increased the prevalence of dry eye disease (DED). Studies show that blink frequency reduced considerably during computer work, hence the tear film is spread less regularly over the anterior surface of the eye giving rise to an unstable tear film. This may lead to tired, dry eyes. The aim of this study was to observe if the tear film quality and dry eye symptoms may improve with the use of the computer animation program BlinkBlink during prolonged computer work. Participating subjects test two versions of the program, whereby one version applies the animation in a much lower frequency, hence serving as a near placebo version. The testing order of the versions is randomized. The variables tested in this study are non-invasive tear film break up (NIBUT) and subjective dry eye symptoms with the Ocular Surface Disease Index (OSDI) questionnaire.

Interventions

DEVICEAnimation program BlinkBlink

Computer program that presents horizontal bars on the computer screen that move from above and below towards each other, mimicking a blink movement.

Sponsors

University of Applied Sciences and Arts Northwestern Switzerland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

The investigator does not know the order of versions tested by participants.

Intervention model description

Subjects use two versions of the program for a set duration, separated by a washout phase. The order of versions applied is randomised.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* duration of computer work of at least six hours per day during at least four days per week * OSDI score ≥ 18 * no active pathology on the anterior eye * Snellen visual acuity of ≥ 0.8.

Exclusion criteria

* acute systemic disease * contact lens wear * asthenopia

Design outcomes

Primary

MeasureTime frameDescription
Subjective improvement of dry eyes14 dayssubjective improvement with OSDI questionnaire
objective improvement of dry eyes14 daysobjective improvement of tear film quality (NIBUT)

Countries

Switzerland

Outcome results

None listed

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