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To Correlate changes in contrast sensitivity with higher order aberrations in patients of Computer Vision Syndrome.

Correlation of central and peripheral contrast sensitivity with higher order aberrations in computer vision syndrome - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/06/069496
Enrollment
106
Registered
2024-06-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Health Condition 1: H189- Unspecified disorder of cornea

Interventions

Control Intervention1: NIL: NIL

Sponsors

Government Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: SUBJECT SELECTION Group 1: Normal Controls Group 2: Patients with Computer Vision Syndrome INCLUSION CRITERIA FOR GROUP 1 1. Age more than 18 and less than 40 years, either gender 2. Best corrected visual acuity of 6/6 and near acuity of N6. 3. No signs or symptoms of CVS 9 INCLUSION CRITERIA FOR GROUP 2 1. Age more than 18 and less than 40 years, either gender 2. Best corrected visual acuity of 6/6 and near acuity of N6. 3. Having a score of more than 6 in the CVS-Q questionnaire

Exclusion criteria

Exclusion criteria: 1. Contact lens use 2. Patients with history of incisional or laser eye surgery 3. Any cause for visual impairment (e.g., glaucoma, cataract more than grade 2 or higher using LOCS III grading (Annexure 3), diabetic retinopathy, Age Related Macular Degeneration, etc.) or media opacities. 4. Patients with amblyopia; strabismus; anisometropia; refractive errors higher than 6 D myopia, 4 D hyperopia, or 4 D astigmatism 5. Any medical condition which in the investigator"s opinion would preclude the patient from providing reliable and valid data (e.g., cognitive impairment, Parkinson"s disease, Alzheimer"s disease and any other neurological or musculoskeletal disease).

Design outcomes

Primary

MeasureTime frame
To compare central and peripheral contrast sensitivity in patients with computer vision syndrome (with and without dry eye disease) and normal controlsTimepoint: in a period of 12 months

Secondary

MeasureTime frame
To correlate changes in contrast sensitivity with higher order aberrations and compare them in between patients with and without CVS.Timepoint: in a period of 12 months

Countries

India

Contacts

Public ContactDr Parul Ichhpujani

Government Medical College and Hospital, Chandigarh

parul77@rediffmail.com9501071591

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026