Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
ID07526025

Comparative Effects of Eye-Cervical Re-Education Exercises and Pressure Biofeedback Training of Deep Cervical Flexors in Cervicogenic Headache

Led by Foundation University Islamabad · Updated on 2026-05-20

34

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cervicogenic headache (CGH) is a type of headache caused by problems in the upper neck spine, especially the atlanto-occipital and C1-C3 segments. It affects the head or face and often worsens with neck movement, causing pain and limited neck motion. This condition involves disrupted neck muscle control and sensing, and it accounts for about 15-20% of chronic headaches. Researchers are comparing two physical therapy methods designed to improve neck muscle control and sensing in patients with CGH to better manage symptoms like pain and disability. The study compares two treatment groups receiving different exercises alongside conventional physical therapy. One group receives eye-cervical re-education exercises that involve ocular mobility, neck movement, and coordination phases. The other group undergoes pressure biofeedback training targeting deep neck muscles, using a device to monitor and guide muscle activation at various pressure levels. Both groups also receive hot packs, isometric neck exercises, and specific joint mobilization techniques. Treatments are given over multiple sessions, with assessments at the start and after the 10th session. Participants will be involved in physical therapy sessions including hot packs, exercises, and specialized training depending on their group. Researchers will measure neck joint position sense (proprioception), pain intensity, neck disability, and range of motion at baseline and after three weeks of treatment. Data collection aims to assess improvements within and between groups to inform better physical therapy practices for CGH. The total study duration includes initial assessment, treatment sessions, and follow-up evaluations.

CONDITIONS

Brief Title

Comparative Effects Of Eye-Cervical Re-Education Exercises And Pressure Biofeedback Training Of Deep Cervical Flexors In Cervicogenic Headache

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 45 years
  • Both genders
  • Unilateral neck pain and referred headache
  • Headache worsens with neck movements or sustained positions
  • Positive cervical flexion rotation test
  • Headache reproduced by provocation of upper cervical segments
  • Restricted mobility in upper cervical spine
Not Eligible

You will not qualify if you...

  • Cervical radiculopathy
  • Known or suspected vestibular disorders such as benign paroxysmal positional vertigo, vestibular neuritis, Meniere's disease, labyrinthitis
  • Visual problems including occipital neuralgia
  • History of traumatic neck injury, neck surgery, or cervical instability
  • Rheumatoid arthritis
  • Osteoporosis
  • Metabolic disorders
  • Spinal infection or tumors
  • Vertebrobasilar insufficiency
  • Other headache types such as tension headache or migraine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 3 weeks

Participants receive either eye-cervical re-education exercises or pressure biofeedback training of deep cervical flexors along with conventional physical therapy including hot packs, isometric exercises, and SNAGs to improve neck pain, range of motion, and joint proprioception.

Multiple visits over 3 weeks

Trial Site Locations

Total: 1 location

1

Foundation University College of Physical Therapy

Islamabad, Punjab Province, Pakistan, 46000

Actively Recruiting

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Research Team

M

Maira Tafzeel, DPT

Q

Quratulain Saeed, MS-OMPT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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