NCT07684183

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
74

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress85%
Nov 2025Sep 2026

Study Start

First participant enrolled

November 15, 2025

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

June 28, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 6, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 15, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 15, 2026

Last Updated

July 27, 2026

Status Verified

September 1, 2025

Enrollment Period

9 months

First QC Date

June 28, 2026

Last Update Submit

July 24, 2026

Conditions

Keywords

Text neck syndromeCervical StabilizationPressure biofeedback unitEyeball exercisesPhysiotherapyRandomized clinical trialpain managementneck disability index

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

EXPERIMENTAL

These patients will receive physiotherapy care along with cervical stabilization exercises and eyeball exercises. Treatment schedule: 3 sessions on alternate days for 6 weeks.

Other: Physiotherapy care, Cervical Stabilization and Eyeball Exercises

Physiotherpy care, Cervical stabilisation and placebo

ACTIVE COMPARATOR

These 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.

Other: Phyisotherapy Care, Cervical Stabilization and placebo exercises

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, Cervical stabilisation and eyeball exercises

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.

Physiotherpy care, Cervical stabilisation and placebo

Eligibility Criteria

Age25 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

MeSH Terms

Conditions

Agnosia

Condition Hierarchy (Ancestors)

Perceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Sahreen Anwar, Ph.D

    University of Lahore

    STUDY CHAIR

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

Locations