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The impact of astigmatic correction with Precision 1 Toric contact lenses on functional vision with digital devices

The impact of astigmatic correction with Precision 1 Toric contact lenses on functional vision with digital devices in healthy participants with low to moderate astigmatism

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622001575729
Enrollment
15
Registered
2022-12-20
Start date
2023-01-30
Completion date
2023-05-24
Last updated
2023-12-12

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

Conditions

None listed

Brief summary

The purpose of this prospective, randomized crossover trial is to understand how Precision 1 Toric contact lenses impact on functional vision with digital devices, in comparison to functional visual performance with spherical equivalent contact lenses (Precision 1 sphere) in healthy participants with low to moderate levels of astigmatism.

Interventions

The intervention is a soft disposable contact lens that provides an optical correction for astigmatism. The lenses will be fit to individual participants' eyes by an experienced (>10 years) research optometrist, to provide optimal correction for their low to moderate astigmatic refractive errors. The astigmatism correcting lens will be worn in both eyes for a single 60-minute session in a research laboratory/clinical facility. The order of lens wear (intervention/control) will be randomized.

The intervention is a soft disposable contact lens that provides an optical correction for astigmatism. The lenses will be fit to individual participants' eyes by an experienced (>10 years) research optometrist, to provide optimal correction for their low to moderate astigmatic refractive errors. The astigmatism correcting lens will be worn in both eyes for a single 60-minute session in a research laboratory/clinical facility. The order of lens wear (intervention/control) will be randomized. All participants will wear the intervention and control lenses in separate sessions on different days at least 24 hours apart (i.e. crossover study design).

Sponsors

Queensland University of Technology
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject)

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy adults with normal corrected visual acuity in each eye Refractive astigmatism between -0.50 and -1.50 D Spherical refractive error of between 0.00 and -6.00 D Normal binocular vision and accommodative function Prior history of successful soft contact lens wear

Exclusion criteria

History of eye disease, surgery, or injury Contraindications to contact lens wear Signs or symptoms of dry eye or ocular surface disease Regular rigid contact lens wear Unable to achieve a satisfactory lens fit with the study contact lenses

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026