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Study of Eye-Related Discomfort and Effectiveness of Vision Therapy as its Management in Young Adults.

Visual Discomfort Profile and Efficacy of Optometric Intervention as a Management Modality in Discomfort Associated with Internal Symptom Factor among a Cohort of Young Adults - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104785
Enrollment
40
Registered
2026-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: H533- Other and unspecified disorders ofbinocular vision

Interventions

Intervention1: Optometric Management Modality: Optometric Management Modality consisting of Optical Correction and Vision Therapy will be carried out for 12 weeks Control Intervention1: NIL: NIL

Sponsors

Dr Reshma Ramakrishnan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants in the age group of 18-35 years Participants with the BCVA 6/6, N6. Participants with Asthenopic symptoms. Participants of either gender Participants who provide consent form and are willing to be part of the study

Exclusion criteria

Exclusion criteria: Participants with known cases of ocular pathologies inclusive of surface disorder Participants with binocular vision anomalies due to constant strabismus, amblyopia, and anisometropia more than 2.00 Diopters Participants with NSBV (Nonstrabismic binocular vision) anomalies on treatment.

Design outcomes

Primary

MeasureTime frame
1. Mean difference in Visual Discomfort Questionnaire and Binocular Vision Dysfunction Questionnaire total scores pre- and post-optometric intervention. 2.Reduction in severity of symptoms related to Internal Symptom Factor 3.Prevalence and type of Symptom Factor Contributing to visual discomfortTimepoint: 12 weeks

Secondary

MeasureTime frame
1.Change in visual attention, reading rate and accuracy parameters before and after intervention. 2.Changes in binocular vision parameters. 3.Association between:Visual Discomfort Questionnaire, Binocular Vision Dysfunction Questionnaire scores and clinical binocular vision findings. 4.Association between Visual discomfort severity and reading/attention performance. 5.Differential improvement in individual symptoms related to the Internal Symptom Factor. Timepoint: 12 weeks

Countries

India

Contacts

Public ContactMisba Khan

MGM Institute of Health Sciences

anandreshma@gmail.com9930007490

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026