Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID07508410

Comparison of the Efficacy of Mulligan Mobilization and Myofascial Release in Patients With Cervicogenic Headache

Led by Konya Beyhekim Training and Research Hospital · Updated on 2026-04-02

90

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cervicogenic headache (CBH) is a type of headache caused by problems in the cervical spine, including bones, discs, or soft tissues, often accompanied by neck pain. This research aims to compare the effects of two therapy methods, Mulligan mobilization and myofascial release, in treating cervicogenic headache through a prospective clinical study involving adults aged 18 to 65 years with symptoms lasting at least three months. The study follows ethical principles and collects detailed patient information including medical history and sociodemographic data. Participants will be randomly assigned to one of three groups. Group one will receive Mulligan mobilization therapy three times weekly for four weeks (12 sessions total) along with a home exercise program. Group two will receive myofascial release therapy on the same schedule plus the home exercises. Group three will follow only the home exercise program, also three times weekly for four weeks. Each therapy session involves specific manual techniques administered by a therapist, and the home exercises focus on neck mobility and strengthening. Throughout the study, patients will be evaluated before treatment, immediately after, and one month after completing therapy. Assessments include headache frequency recorded in a diary, pain intensity using a visual analog scale, and functional status via the headache impact test. Headache-related disability and quality of life will also be measured using standardized questionnaires. Weekly phone calls will support exercise adherence, and the study monitors outcomes to assess therapy effectiveness and patient quality of life over time.

CONDITIONS

Brief Title

Comparison of the Eficacy of Mulligan Mobilization and Myofascial Release in Patients With Cervicogenic Headache

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 18 to 65 years
  • Neck or headache symptoms lasting at least 3 months
  • Diagnosis of cervicogenic headache including unilateral pain
  • Reduced neck range of motion
  • Ipsilateral shoulder or arm discomfort
  • Pain worsened by neck movements and tender to touch
Not Eligible

You will not qualify if you...

  • Migraine or cluster headache
  • Cervical radiculopathy or entrapment neuropathy
  • Myelopathy or rheumatoid arthritis
  • Previous cervical spinal surgery
  • Pregnant women
  • Physical therapy within the last 6 months
  • History of major psychiatric illness
  • Uncontrolled cardiovascular, pulmonary, hepatic, renal, hematological diseases
  • Uncontrolled endocrine diseases such as diabetes or hyperthyroidism

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 - 4 weeks

Participants receive their assigned therapy: Mulligan mobilization therapy, myofascial release therapy, or a home exercise program, each conducted three times a week for four weeks (12 sessions total).

Three sessions per week for 4 weeks (12 sessions total)

Follow-up

Duration - 1 month

Participants are evaluated immediately after treatment and one month later to assess headache frequency, pain intensity, functional status, disability, and quality of life.

2 visits (in-person) after treatment completion

Trial Site Locations

Total: 1 location

1

Konya Beyhekim Eğitim ve Araştırma Hastanesi

Konya, Turkey (Türkiye), 42060

Actively Recruiting

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Research Team

B

BURCU VURAL

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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