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CompletedNCT06871865Updated Jul 18, 2025

The Effects of Oculomotor Training on Pain, Cervical Range of Motion, Joint Position Sense, Endurance, and Balance in Individuals With Mechanical Neck Pain

An interventional study of Oculomotor Exercises and Posture Exercises in Mechanical Neck Pain, sponsored by Zonguldak Bulent Ecevit University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2025-07-18.

Sponsored by Zonguldak Bulent Ecevit University · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

The aim of this study was to investigate the effects of oculomotor training on pain, cervical range of motion, joint position sense, endurance and balance in individuals with mechanical neck pain.

02

Conditions studied

  • Mechanical Neck Pain

Keywords

  • Mechanical neck pain
03

In context

Lead sponsor

Zonguldak Bulent Ecevit University is the lead sponsor of 96 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diagnosed with mechanical neck pain
  • Neck pain lasting longer than 3 weeks
  • Individuals aged 18-50 years
  • Score of 5 or higher on the Neck Disability Index

Exclusion criteria

Exclusion Criteria:

  • Having received physical therapy in the last 6 months
  • Presence of congenital anomaly on cervical radiography
  • Neurological deficit detected in physical examination
  • Diagnosis of vertebrobasilar artery insufficiency
  • Diagnosis of vestibular disease
  • Presence of a rheumatic disease
  • Presence of structural scoliosis
  • History of spinal surgery
  • Pregnancy
  • Malignancy
  • Eye disease/strabismus other than refractive errors
  • Active use of anti-inflammatory medication
  • Any mental condition that may prevent adherence to exercises
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    Intervention Group

    This group will be given a home program including isometric neck strengthening exercises, neck stretching exercises and posture exercises during the 6-week treatment period, and the control group will be given an additional oculomotor exercise program.

    Other: Oculomotor Exercises · Other: Posture Exercises · Other: Neck Stretching and Strengthing Exercises

  • Active comparator
    Control Group

    This group will be given a home program including isometric neck strengthening exercises, neck stretching exercises and posture exercises during the 6-week treatment period.

    Other: Posture Exercises · Other: Neck Stretching and Strengthing Exercises

Interventions

  • OtherOculomotor Exercises

    Oculomotor exercises are designed to improve eye movement control, coordination, and visual tracking.

  • OtherPosture Exercises

    Postural exercises help strengthen core muscles, improve alignment, and enhance stability. They are essential for maintaining proper posture, preventing pain, and reducing the risk of musculoskeletal imbalances.

  • OtherNeck Stretching and Strengthing Exercises

    Neck stretching and strengthening exercises help improve flexibility, reduce stiffness, and enhance muscle support for the cervical spine. They are beneficial for relieving neck pain, improving posture, and preventing injuries.

06

What researchers measure

Primary outcomes

  1. Visual Analog Scale

    Time frame: From enrollment to the end of treatment at 6 weeks

Secondary outcomes

  1. Neck Disability Index

    Time frame: From enrollment to the end of treatment at 6 weeks

  2. Craniovertebral Angle

    Time frame: From enrollment to the end of treatment at 6 weeks

  3. Cervical ROM

    Flexion, extension, lert-right rotation, left-right lateral flexion will be measured.

    Time frame: From enrollment to the end of treatment at 6 weeks

  4. Craniocervical Flexion Test

    Endurance of the deep cervical flexor muscles will be measured.

    Time frame: From enrollment to the end of treatment at 6 weeks

  5. Y Balance Test

    Y Bavlance Test will be applied to test the ability to reach of upper extremity.

    Time frame: From enrollment to the end of treatment at 6 weeks

  6. Beck Depression Inventory

    Time frame: From enrollment to the end of treatment at 6 weeks

07

Study locations

1 site
  • Zonguldak Bülent Ecevit University
    Zonguldak, Zonguldak Province 67100, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06871865
Lead sponsor
Zonguldak Bulent Ecevit University
Responsible party
Eda AKBAŞ (Associate Professor, Zonguldak Bulent Ecevit University) — Principal investigator
First posted
Mar 12, 2025
Start date
Mar 3, 2025
Primary completion
Jun 5, 2025
Completion
Jun 23, 2025
Last update
Jul 18, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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