Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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)
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
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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