Yogic Eye Exercises for Computer Vision Syndrome in Female Design Students
Effect of a Four-Week Yogic Eye Exercise Program on Computer Vision Syndrome Symptoms in Female University Students: A Single-Arm Pre-Post Study
2 other identifiers
interventional
36
1 country
1
Brief Summary
Computer vision syndrome (CVS) is a cluster of eye and musculoskeletal complaints - dryness, redness, blurred vision, foreign body sensation, excessive tearing, and neck, shoulder or back pain - that arises from prolonged work at a digital display. It is common among university students, and optical, pharmacological and nutritional treatments have given inconsistent results. Yoga-based eye exercises have been proposed as a brief, inexpensive alternative that requires no equipment. This study tested whether a short, structured programme of yogic eye exercises reduces self-reported CVS symptoms in female undergraduates in a graphic design and digital media programme, a group whose coursework demands sustained, colour-critical near work at a screen. All 36 female students enrolled in the programme took part. Each attended one supervised training session and then performed a 13-minute sequence of relaxation exercises (slow blinking, gazing at a distant target, acupressure around the eyes) and strengthening exercises (eye rolling, nose-tip gazing) three days a week for four weeks, a total of 12 sessions, reporting completion of each session on the same day. Nine symptoms - five ocular and four musculoskeletal - were rated on a four-point scale (never, rarely, sometimes, always) at the start and again at the end of week 4. The main question was whether the average of all nine ratings fell over the four weeks. Every participant served as her own comparison; there was no control group and no masking.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2021
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 15, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 16, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
April 16, 2021
CompletedFirst Submitted
Initial submission to the registry
September 7, 2026
CompletedFirst Posted
Study publicly available on registry
September 11, 2026
CompletedSeptember 16, 2026
September 1, 2026
1 month
September 7, 2026
September 13, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline in total symptom score at week 4
Arithmetic mean of all nine self-reported symptom items - five ocular (eye dryness, red eye, foreign body sensation, blurred vision, excessive tearing) and four musculoskeletal (shoulder pain, back pain, loss of sensation in the fingers, loss of sensation in the hands) - each rated on a 4-point Likert scale (1 = never, 2 = rarely, 3 = sometimes, 4 = always). The total score ranges from 1 to 4; lower scores indicate fewer symptoms. Collected by self-completed electronic questionnaire.
Baseline and week 4
Secondary Outcomes (3)
Change from baseline in ocular symptom domain score at week 4
Baseline and week 4
Change from baseline in muscular symptom domain score at week 4
Baseline and week 4
Change from baseline in each individual symptom item at week 4
Baseline and week 4
Other Outcomes (1)
Baseline screen-use behaviour
Baseline
Study Arms (1)
Yogic eye exercise programme
EXPERIMENTALAll participants received the same intervention: a 13-minute session of yogic relaxation and strengthening eye exercises, performed three days per week for four consecutive weeks (12 sessions).
Interventions
A 13-minute sequence performed three days per week for four consecutive weeks (12 sessions in total). Relaxation component: slow blinking; gazing at a fine detail of a distant target; acupressure massage of periocular points. Strengthening component: eye-rolling movements; nose-tip gazing (focus on the extended thumb, move it slowly toward the nose tip, hold five seconds, move away; repeat twice, approximately 25 seconds per cycle). Delivery: one supervised group training session before baseline, written and illustrated instructions, then independent home practice with same-day reporting of each completed session in a monitored group thread.
Eligibility Criteria
You may qualify if:
- Female undergraduate enrolled in the Graphic Design and Digital Media programme at Princess Nourah bint Abdulrahman University
- Use of a computer for at least one month before the study
- Able to read and understand English
- Provided written informed consent
You may not qualify if:
- Diagnosis of Sjögren syndrome
- Diagnosis of keratoconjunctivitis sicca
- Use of medications known to reduce tear production, for example antihistamines
- Use of isotretinoin
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- King Saud Universitylead
- Princess Nourah Bint Abdulrahman Universitycollaborator
Study Sites (1)
: Princess Nourah bint Abdulrahman University
Riyadh, 11671, Saudi Arabia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr.
Study Record Dates
First Submitted
September 7, 2026
First Posted
September 11, 2026
Study Start
March 15, 2021
Primary Completion
April 16, 2021
Study Completion
April 16, 2021
Last Updated
September 16, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, CSR, ANALYTIC CODE
- Time Frame
- Available on request from the date of publication, indefinitely.
- Access Criteria
- Requests should be directed to the corresponding author and will be considered on reasonable scientific grounds.
The de-identified participant-level dataset and the analysis code that support the findings are held by the corresponding author.