Actively Recruiting
Comparison of the Eficacy 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 defined as a headache caused by a disorder in the cervical spine, bones, discs, or soft tissue elements, which is also accompanied by neck pain. Unilateral, non-reversible oculo, fronto, temporal pain, pain that increases with poor neck positioning and incorrect neck movements, and may be seen with restricted movement in the upper cervical and occiput regions. The aim of this thesis is to compare the effectiveness of Mulligan mobilization technique and myofascial release methods used in the treatment of cervicogenic headache through a prospective clinical study.
CONDITIONS
Official 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 with unilateral pain
- Reduced neck range of motion
- Ipsilateral shoulder or arm discomfort
- Pain worsened by neck movement and painful on palpation
You will not qualify if you...
- Diagnosis of migraine or cluster headache
- Cervical radiculopathy or entrapment neuropathy
- Myelopathy or rheumatoid arthritis
- Previous cervical spinal surgery
- Pregnancy
- Physical therapy received within the last 6 months
- History of major psychiatric illness
- Uncontrolled systemic diseases (cardiovascular, pulmonary, hepatic, renal, hematological)
- Uncontrolled systemic endocrine diseases such as diabetes or hyperthyroidism
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Konya Beyhekim Eğitim ve Araştırma Hastanesi
Konya, Turkey (Türkiye), 42060
Actively Recruiting
Research Team
B
BURCU VURAL
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here