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Clinical Trials/NCT04637516
NCT04637516CompletedNot Applicable

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

University of Applied Sciences and Arts Northwestern Switzerland1 site in 1 country30 target enrollmentStarted: April 1, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Subjective improvement of dry eyes

Study Overview

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.

Study Design

Study Type
Interventional
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.

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts 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

Arms & Interventions

Programme Version 60 sec frequency

Active Comparator

This version of the program "BlinkBlink" has a presentation frequency of 60 sec

Intervention: Animation program "BlinkBlink" (Device)

Programme Version 300 sec frequency

Placebo Comparator

This version of the program "BlinkBlink" has a presentation frequency of 300 sec

Intervention: Animation program "BlinkBlink" (Device)

Outcomes

Primary Outcomes

Subjective improvement of dry eyes

Time Frame: 14 days

subjective improvement with OSDI questionnaire

objective improvement of dry eyes

Time Frame: 14 days

objective improvement of tear film quality (NIBUT)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Daniela Nosch

Professor

University of Applied Sciences and Arts Northwestern Switzerland

Study Sites (1)

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