Eyeball Exercises and Cervical Stabilization in Text Neck Syndrome
Effects of Eyeball Exercises and Cervical Stabilization in Text Neck Syndrome: a Randomized Clinical Trial
1 other identifier
interventional
74
1 country
1
Brief Summary
The prolonged use of electronic devices in the population nowadays contributes to the development of various musculoskeletal disorders affecting the neck. One such condition is the Text neck syndrome characterized by neck pain and muscular imbalance in the region as well as development of forward head posture. Some additional symptoms include headaches, impaired range of motion and eye strain. Eyeball exercises have been shown to improve symptoms of neck pain, and cervical stabilization has demonstrated positive effects on the deep cervical flexors, thereby improving forward head posture and other neck-associated symptoms. However, the combined effect of these two interventions has not been studied to treat text neck syndrome before. The primary outcome measures include the pain measured through Numeric Pain Rating Scale (NPRS) and pain pressure threshold (algometer), whereas the secondary outcome measures include the craniovertebral angle (CVA) and functional disability measured through neck disability index (NDI).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
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
November 15, 2025
CompletedFirst Submitted
Initial submission to the registry
June 28, 2026
CompletedFirst Posted
Study publicly available on registry
July 6, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 15, 2026
July 27, 2026
September 1, 2025
9 months
June 28, 2026
July 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Pain Intensity
Change in pain intensity measured using the Numeric Pain rating Scale (NPRS, 0-10 cm). Lower limit: 0 Upper limit: 10 Lower value means less pain
Baseline, at 3rd week and at 6th week
Neck Disability
Functional disability measured using the Neck Disability Index (NDI) - Urdu validated version. Lower limit: 0 Upper limit: 50 Lower value indicates lesser disability
Baseline, at 3rd week and at 6th week
Secondary Outcomes (2)
Craniovertebral Angle (CVA)
Baseline, at 3rd week and at 6th week
Pain Pressure Threshold (PPT)
Baseline, at 3rd week and at 6th week
Study Arms (2)
Physiotherapy care, Cervical stabilisation and eyeball exercises
EXPERIMENTALThese patients will receive physiotherapy care along with cervical stabilization exercises and eyeball exercises. Treatment schedule: 3 sessions on alternate days for 6 weeks.
Physiotherpy care, Cervical stabilisation and placebo
ACTIVE COMPARATORThese patients will receive physiotherapy care along with cervical stabilization exercises and placebo treatment in place of eyeball exercises. Treatment schedule: 3 sessions on alternate days for 6 weeks.
Interventions
Physiotherapy care: 30minutes of physiotherapy, including hotpack for 10 minutes,cervical stretching (3sets/15-second hold,5 repetitions), cervical isometrics (5-10 reps/3sets), postural correction exercises (5-10 reps/2-3 sets), active ROMs of the neck.•Cervical Stabilization: Pressure biofeedback unit will be used, the patient will perform chin tucks while the inflated unit is below the head at 20mmHg initially, and will be raised to 30mmHg. A 10 seconds hold with 10 repetitions, including a 10-second rest interval between. A total of 3sets will be performed with 15second interval between each set. 15 minutes total •Eyeball exercises:The patient is then asked to carry out the described eyeball movements, each movement to be held for 10 seconds and repeated 4 times through the maximum range,directions: Leftward, rightward, upper left, lower left, upper and lower right, left and right side circular, leftward and rightward figure 8 rotation. 2sets with 15seconds interval. 15 mins total.
Physiotherapy care:30minutes of physiotherapy, including hotpack for 10 minutes, cervical stretching(3sets/15second hold, 5reps), cervical isometrics(5-10 reps/3sets), postural correction exercises(5-10 reps/2-3 sets), active ROMs of the neck.•Cervical stabilization: Pressure biofeedback unit will be used, the patient will perform chin tucks while the inflated unit is below the head at 20mmHg initially, and will be raised to 30mmHg. A10seconds hold with 10 repetitions, including a 10second rest interval between. A total of 3sets will be performed with 15second interval between each set,15 minutes total. •Placebo treatment:These exercises will take 10-15 minutes and the purpose is to engage the patient. These exercises do not have any effect on the ocular muscle of the eye and will only serve as a source of relaxation and lubrication for the eyes of the patient: blink slowly \& fully (10reps,3sets with10-15seconds interval), fix gaze (10seconds, 3-5reps), eyes closed breathing 60seconds.
Eligibility Criteria
You may qualify if:
- Neck Disability Index (NDI) scoring: \>5 and \<24
- Duration of screen usage: 4-6 hours/day
- Pain: ranging from mild - moderate 4-7 Numeric Pain Rating Scale (NPRS)
You may not qualify if:
- Already undergoing physical therapy
- Cervical trauma, radiculopathy, pregnancy, malignancies, torticollis, herniation, stenosis, osteoporosis, etc
- Diagnosed with a CNS abnormality
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Lahore Teaching Hospital
Lahore, Punjab Province, 54782, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Sahreen Anwar, Ph.D
University of Lahore
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 28, 2026
First Posted
July 6, 2026
Study Start
November 15, 2025
Primary Completion (Estimated)
August 15, 2026
Study Completion (Estimated)
September 15, 2026
Last Updated
July 27, 2026
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share