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Efficacy of blink software in improving the blink rate and dry eye symptoms in visual display terminal users - A
D L Ashwini1, Ramesh S Ve2, Daniela Nosch3
1Department of Optometry, Manipal College of Health Professions, Manipal Academy of Higher Education, Manipal, Udupi; Sankara College of Optometry, Sankara Eye Hospital, Bengaluru, Karnataka, India.
Purpose:
Dry eye disease (DED) is a multifactorial disease, more prevalent among visual display terminal users. Reduced blink rate is a risk factor to dry eye disorder, innovative means to remind to blink while using computers can be helpful.
Methods:
Single-blinded Randomized Control Trial enrolled computer users with dry eye. Allocation concealment was done using opaque envelope and principal investigator was blinded. After baseline examination, eligible participants were randomized to intervention group (appearance of bars is 8 times/min) and control group (appearance of bars is 1 time/min). Participants from both groups used the software for 15 days, came for first follow up, and did not use the software for next 15 days until second follow-up examination. During each visit, detailed eye examination was done including blink rate, tear film break up time, and Ocular Surface Disease Index score.
Results:
Forty-six participants (women n = 31; men n = 15) with a mean age of 28.02 (±6.295) years completed the study. Four participants were excluded from analysis because of early dropout. In the intervention group (n = 23) and control group (n = 23), participants were allocated. At the end of first phase, there was statistically significant difference in OSDI score (P = 0.021). Statistically significant difference was noticed in OSDI (P = 0.014) and blink rate (P = 0.049) as baseline, and final visit data were compared.
Conclusion:
"Blink-Blink" software with 8 reminders/min improved DED-related symptoms by increasing the blink rate. The carry-over effect after cessation of Blink-Blink software in improving blink rate was maintained even after 1 month.
Trial Registration:
: Clinical Trials Registry-India (CTRI): CTRI/2018/08/015176.
