Comparison of Two Contact Lens Designs

The proposed study will address this gap by comparing the efficacy of two novel stenfilcon A contact lens designs in alleviating accommodative burden associated with digital device usage. The primary outcomes are measured with the following: * Computer vision syndrome questionnaire * Binocular logMar (H/Lo contrast) visual acuity at 6M and 40cm. * Binocular range of clear vision * Subjective assessment of accommodation * Objective assessment of accommodation Subjects will be randomly assigned to wear one contact lens design for 5 days. Then crossed over tot he opposing design after a three day washout period, and again asked to wear the lens for 5 days.

NCT Number	NCT07488208
Lead Sponsor	Southern College of Optometry
Conditions	Computer Vision Syndrome, Accommodation
Enrollment	30 participants
Start Date	2025-05-22
Primary Completion	2025-09-02 (estimated)
Study Completion	2025-09-02 (estimated)
Updated on ClinicalTrials.gov	2026-03-25