ClinicalTrials.Veeva

Menu

Effects of Blue of Glasses VS Standard Lenses on Contrast Sensitivity & Visual Fatigue in Myopic & Non-Myopic Adults

S

Superior University

Status

Active, not recruiting

Conditions

Myopia

Treatments

Diagnostic Test: Standard Lenses (Control Group)
Combination Product: Blue Light-Blocking Glasses (Intervention Group)

Study type

Interventional

Funder types

Other

Identifiers

NCT06739525
MSRSW/Batch-Fall22/749

Details and patient eligibility

About

This study investigates the effects of blue light-blocking glasses compared to standard lenses on contrast sensitivity and visual fatigue in myopic and non-myopic adults. With the growing use of digital screens, blue light exposure has raised concerns due to potential eye strain, sleep disruption, and visual fatigue.

Full description

While blue light-blocking lenses are marketed to address these issues, evidence of their efficacy, particularly for different refractive errors like myopia, remains inconclusive. Using a randomized controlled design, this study will assess both groups across specific visual tasks to measure contrast sensitivity and visual fatigue. Outcomes are evaluated using validated tools, including the Computer Vision Syndrome Questionnaire (CVS-Q) and Visual Fatigue Questionnaire (VFQ), with measurements taken at baseline, 2 weeks, and 4 weeks. Findings are expected to clarify the potential advantages of blue light-blocking glasses over standard lenses, aiding in evidence-based recommendations for adults with varying visual needs.

Enrollment

64 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults aged 18-50 years.
  • Both myopic (with any degree of myopia) and non-myopic adults.
  • Participants who use computer screens for at least four hours per day.
  • Individuals currently using corrective lenses or willing to wear study-provided glasses during the experiment.
  • Individuals willing to complete the study protocol, which includes attending follow-up examinations and filling out visual fatigue questionnaires.

Exclusion criteria

  • A history of any serious vision-related condition (such as glaucoma, cataracts, or retinal problems).
  • Individuals who have already undergone refractive surgery (e.g., LASIK) or other types of eye surgery.
  • Systemic conditions affecting vision include diabetes, neurological problems, and any other ailment that may impair visual ability.
  • Taking drugs that are known to impair vision or produce visual tiredness (for example, certain antihistamines and antidepressants).
  • Pregnant women's visual performance may be affected by hormonal changes.
  • People with uncorrected vision difficulties cannot use the prescription lenses during study time.
  • Participants who are allergic or sensitive to lens materials.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

64 participants in 2 patient groups

interventional group
Experimental group
Treatment:
Combination Product: Blue Light-Blocking Glasses (Intervention Group)
Control Group
Active Comparator group
Treatment:
Diagnostic Test: Standard Lenses (Control Group)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems